Reactions & Stoichiometry

General Chemistry · Dr. Karmach

Dr. Karmach

By the end of this unit, you can…

  • Balance any chemical equation with the smallest whole-number coefficients
  • Read a balanced equation as a recipe: coefficients are mole relationships
  • Convert between amounts of any two species using mole ratios
  • Chain molar masses with mole ratios to solve gram-to-gram problems
  • Identify which reactant limits a reaction and how much product it allows
  • Classify a reaction by type and cite the evidence that a reaction occurred
  • Apply the solubility rules to predict precipitates and assign physical states
  • Write molecular, complete ionic, and net ionic equations and classify electrolytes
  • Assign oxidation numbers and identify oxidizing and reducing agents
  • Write half-reactions and use the activity series to predict single displacement
  • Carry molarity through stoichiometric calculations and compute percent yield
  • Find an unknown concentration, mass percent, or formula from one measurement
Dr. Karmach

Today's route 🗺️

  1. Balancing Equations
  2. Types of Reactions
  3. Solubility Rules & Precipitation
  4. Net Ionic Equations
  5. Electrolytes & Dissociation
  6. Acids and Bases, Strong vs Weak
  7. Oxidation Numbers
  8. Oxidizing & Reducing Agents
  9. The Activity Series
  10. Mole Ratios
  11. Mass-to-Mass Stoichiometry
  12. Limiting Reactant
  13. Percent Yield
  14. Solution Stoichiometry
  15. Quantitative Analysis
Dr. Karmach

1 · Balancing Equations

Turn any skeleton equation into a balanced one, and identify which numbers may change.

Dr. Karmach

Atoms don't disappear

Burning methane makes new molecules out of the same atoms. Count them: 1 C, 4 H, 4 O before and after. Every reaction works this way.

Dr. Karmach

What an equation says

CH₄(g) + 2 O₂(g) → CO₂(g) + 2 H₂O(g)
reactants → products  ·  the arrow reads "react to form"  ·  each + reads "and"
"methane and oxygen react to form carbon dioxide and water"
(s) solid  ·  (l) liquid  ·  (g) gas  ·  (aq) aqueous, dissolved in water

An equation is a sentence about substances. Formulas right, coefficients not yet chosen: that is a skeleton equation. Balancing supplies the coefficients; nothing else may change.

Dr. Karmach

Your turn: count atoms in 3 Mg(OH)₂

Sixty seconds, straight from the naming rules: parentheses multiply, and now a coefficient multiplies the whole formula.

atom count
Mg 3 × 1 =
O 3 × =
H 3 × =
Dr. Karmach

Your turn: count atoms in 3 Mg(OH)₂

Sixty seconds, straight from the naming rules: parentheses multiply, and now a coefficient multiplies the whole formula.

atom count
Mg 3 × 1 =
O 3 × =
H 3 × =
3 Mg(OH)₂
Mg: 3 × 1 = 3  ·  O: 3 × 2 = 6  ·  H: 3 × 2 = 6

The coefficient 3 multiplies every atom in the formula; the subscript 2 multiplies only what the parentheses enclose.

Dr. Karmach

Why every equation must balance

A reaction rearranges atoms. It never creates or destroys them. Both sides of a correct equation must show the same number of each kind of atom.

2 H₂ + O₂ → 2 H₂O
H: 4 = 4 ✓  ·  O: 2 = 2 ✓  ·  a possible reaction
H₂ + O₂ → H₂O
H: 2 = 2 ✓  ·  O: 2 ≠ 1 ✗  ·  an O atom would have to vanish
Dr. Karmach

What "balanced" looks like

2 KClO₃ → 2 KCl + 3 O₂
K: 2 = 2 ✓  ·  Cl: 2 = 2 ✓  ·  O: 6 = 6 ✓

Every element's count matches. That is the complete test.

Dr. Karmach

The method

  1. Write the atom count for each side.
  2. Balance one element at a time. Save any element that appears in several formulas for last.
  3. Recheck every count after each change.
  4. Finish with the smallest whole numbers.
Dr. Karmach

Worked example 1: splitting water

Step 1 · Write the atom count for each side

H₂O → H₂ + O₂  (skeleton)
H: 2 = 2 ✓  ·  O: 1 ≠ 2 ✗

Electrolysis splits water into hydrogen gas and oxygen gas. Oxygen doesn't balance.

A common first attempt: change H₂O to H₂O₂. Test it.

Dr. Karmach

Worked example 1: solution

H₂O → H₂ + O₂  (skeleton)
H: 2 = 2 ✓  ·  O: 1 ≠ 2 ✗

A common first attempt

H₂O₂ → H₂ + O₂
H: 2 = 2 ✓  ·  O: 2 = 2 ✓

Every count matches. But H₂O₂ is hydrogen peroxide. The goal was to split water; this equation splits a different substance. Changing a subscript changed the chemistry.

Dr. Karmach

Worked example 1: solution

H₂O → H₂ + O₂  (skeleton)
H: 2 = 2 ✓  ·  O: 1 ≠ 2 ✗
A common first attempt
H₂O₂ → H₂ + O₂
H: 2 = 2 ✓  ·  O: 2 = 2 ✓
Step 2 · Balance one element at a time

Coefficients, not subscripts:

2 H₂O → 2 H₂ + O₂
H: 4 = 4 ✓  ·  O: 2 = 2 ✓
Dr. Karmach

Worked example 1: solution

H₂O → H₂ + O₂  (skeleton)
H: 2 = 2 ✓  ·  O: 1 ≠ 2 ✗
A common first attempt
H₂O₂ → H₂ + O₂
H: 2 = 2 ✓  ·  O: 2 = 2 ✓
Step 2 · Balance one element at a time
2 H₂O → 2 H₂ + O₂
H: 4 = 4 ✓  ·  O: 2 = 2 ✓
Coefficients change the amount. Subscripts change the substance. Only coefficients may change.
Dr. Karmach

Worked example 1: the route

2 H₂O → 2 H₂ + O₂
found: H: 4 = 4 ✓  ·  O: 2 = 2 ✓

H₂O is the only compound, so O went first: 2 H₂O. H₂, a free element, took the last coefficient: 2 H₂. The recheck found every count equal, so no step repeated.
Dr. Karmach

Take-home: coefficients, not subscripts

An equation holds two kinds of numbers with different jobs. A coefficient counts molecules; a subscript is part of the formula. Balancing may change only the coefficients.

Dr. Karmach

Worked example 2: a common multiple

Rust: iron reacting with oxygen.

Step 1 · Write the atom count for each side

Fe + O₂ → Fe₂O₃  (skeleton)
Fe: 1 ≠ 2  ·  O: 2 ≠ 3

Oxygen shows 2 on the left and 3 on the right. What is the smallest number both divide into?

Dr. Karmach

Worked example 2: solution

Fe + O₂ → Fe₂O₃  (skeleton)
Fe: 1 ≠ 2  ·  O: 2 ≠ 3

Step 2 · Balance one element at a time

O first, using the common multiple, 6: write 3 O₂ and 2 Fe₂O₃.

Fe + 3 O₂ → 2 Fe₂O₃
O: 6 = 6 ✓  ·  Fe: 1 ≠ 4 ✗

Fixing O changed the Fe count.

Dr. Karmach

Worked example 2: solution

Fe + O₂ → Fe₂O₃  (skeleton)
Fe: 1 ≠ 2  ·  O: 2 ≠ 3
Step 2 · Balance one element at a time
Fe + 3 O₂ → 2 Fe₂O₃
O: 6 = 6 ✓  ·  Fe: 1 ≠ 4 ✗
Step 3 · Recheck every count

The recheck shows Fe unbalanced. Write 4 Fe:

4 Fe + 3 O₂ → 2 Fe₂O₃
Fe: 4 = 4 ✓  ·  O: 6 = 6 ✓
Dr. Karmach

Worked example 2: solution

Fe + O₂ → Fe₂O₃  (skeleton)
Fe: 1 ≠ 2  ·  O: 2 ≠ 3
Step 2 · Balance one element at a time
Fe + 3 O₂ → 2 Fe₂O₃
O: 6 = 6 ✓  ·  Fe: 1 ≠ 4 ✗
Step 3 · Recheck every count
4 Fe + 3 O₂ → 2 Fe₂O₃
Fe: 4 = 4 ✓  ·  O: 6 = 6 ✓
One change can unbalance an element already counted. Recheck every count after each change.
Dr. Karmach

Worked example 2: the route

4 Fe + 3 O₂ → 2 Fe₂O₃
found: Fe: 4 = 4 ✓  ·  O: 6 = 6 ✓

Fe₂O₃ is the busiest formula, so O went first, with the common multiple 6. The recheck caught Fe, and the free element took the last coefficient: 4 Fe.
Dr. Karmach

Your turn: zinc and hydrochloric acid

Zn + HCl → ZnCl₂ + H₂
atom left right
Zn 1 1 ✓
H × 1 2
Cl × 1 2

One coefficient balances both H and Cl.

Dr. Karmach

Your turn: zinc and hydrochloric acid

Zn + HCl → ZnCl₂ + H₂
atom left right
Zn 1 1 ✓
H × 1 2
Cl × 1 2

One coefficient balances both H and Cl.

Zn + 2 HCl → ZnCl₂ + H₂
Zn: 1 = 1 ✓  ·  H: 2 = 2 ✓  ·  Cl: 2 = 2 ✓
Dr. Karmach

Where this goes wrong

Changing subscripts. Writing H₂O₂ balances the counts but changes the substance. If the formula changes, the chemistry changes.
Forgetting the unwritten 1. Zn + 2 HCl → ZnCl₂ + H₂ has coefficient sum 1 + 2 + 1 + 1 = 5, not 4. An unwritten coefficient is still a 1.
Reading coefficients as grams. 4 Fe + 3 O₂ does not mean "4 g and 3 g." Coefficients count particles or moles. Converting to mass requires the molar mass.
Stopping too early. 8 Fe + 6 O₂ → 4 Fe₂O₃ balances, but every coefficient divides by 2. Reduce to smallest whole numbers.
Dr. Karmach

Practice 1

4 NH₃ + 5 O₂ → 4 NO + 6 H₂O

Ammonia burned over a platinum catalyst, the first step in making nitric acid for fertilizer. What does the 5 in front of O₂ mean?

  1. Each O₂ molecule contains 5 oxygen atoms.
  2. 5 molecules of O₂ react, or equally 5 moles, in proportion to the other coefficients.
  3. 5 grams of O₂ are consumed.
  4. Exactly 5 individual molecules react. The number cannot scale up to moles.
Dr. Karmach

Practice 1: answer B

4 NH₃ + 5 O₂ → 4 NO + 6 H₂O
5 O₂ → 5 × 2 = 10 O  ·  right side: 4 NO + 6 H₂O → 4 + 6 = 10 O ✓

A describes a subscript's job. C: coefficients are counts, never masses. D: multiplying every coefficient by Avogadro's number leaves the ratios unchanged, so coefficients count moles as well as molecules.

In 5 O₂, the coefficient and the subscript do different jobs: 5 × 2 = 10 atoms of O.
Dr. Karmach

Worked example 3: combustion

Stove gas is methane, and burning it makes carbon dioxide and water. The skeleton:

Step 1 · Write the atom count for each side

CH₄ + O₂ → CO₂ + H₂O  (skeleton)
C: 1 = 1 ✓  ·  H: 4 ≠ 2  ·  O: 2 ≠ 3

For combustion, balance C first, H second, O last. O₂ contains only one element, so its coefficient can be set last without disturbing the others.

Balance it.

Dr. Karmach

Worked example 3: solution

CH₄ + O₂ → CO₂ + H₂O  (skeleton)

Step 2 · Balance one element at a time

C first: 1 = 1 already. H second: 4 H on the left need 2 H₂O.

CH₄ + O₂ → CO₂ + 2 H₂O
C: 1 = 1 ✓  ·  H: 4 = 4 ✓  ·  O: 2 ≠ 4 ✗
Dr. Karmach

Worked example 3: solution

CH₄ + O₂ → CO₂ + H₂O  (skeleton)
Step 2 · Balance one element at a time
CH₄ + O₂ → CO₂ + 2 H₂O
C: 1 = 1 ✓  ·  H: 4 = 4 ✓  ·  O: 2 ≠ 4 ✗
Step 3 · Recheck every count

O last: the right side holds 2 + 2 = 4 O, and each O₂ supplies 2. Write 2 O₂.

CH₄ + 2 O₂ → CO₂ + 2 H₂O
C: 1 = 1 ✓  ·  H: 4 = 4 ✓  ·  O: 4 = 4 ✓
Dr. Karmach

Worked example 3: solution

CH₄ + O₂ → CO₂ + H₂O  (skeleton)
Step 2 · Balance one element at a time
CH₄ + O₂ → CO₂ + 2 H₂O
C: 1 = 1 ✓  ·  H: 4 = 4 ✓  ·  O: 2 ≠ 4 ✗
Step 3 · Recheck every count
CH₄ + 2 O₂ → CO₂ + 2 H₂O
C: 1 = 1 ✓  ·  H: 4 = 4 ✓  ·  O: 4 = 4 ✓
4 is even, so O₂ lands cleanly: no fractions, smallest whole numbers on the first pass. Saving the lone-element formula for last meant one clean choice at the end.
Dr. Karmach

Worked example 3: the route

CH₄ + 2 O₂ → CO₂ + 2 H₂O
found: C: 1 = 1 ✓  ·  H: 4 = 4 ✓  ·  O: 4 = 4 ✓

CH₄ is the busiest formula: C, then H. O₂ is a free element, so its coefficient came last and changed no other count. Nothing sent the solution back.
Dr. Karmach

Worked example 4: a fraction appears

Butane fuels lighters.

Step 1 · Write the atom count for each side

C₄H₁₀ + O₂ → CO₂ + H₂O  (skeleton)
C: 4 ≠ 1  ·  H: 10 ≠ 2  ·  O: 2 ≠ 3

Same order: C first, H second, O last.

Balance it. A fraction will appear along the way.

Dr. Karmach

Worked example 4: solution

C₄H₁₀ + O₂ → CO₂ + H₂O  (skeleton)

Step 2 · Balance one element at a time

C first: write 4 CO₂. Then H: write 5 H₂O.

C₄H₁₀ + O₂ → 4 CO₂ + 5 H₂O
C: 4 = 4 ✓  ·  H: 10 = 10 ✓  ·  O: 2 ≠ 13 ✗
Dr. Karmach

Worked example 4: solution

C₄H₁₀ + O₂ → CO₂ + H₂O  (skeleton)
Step 2 · Balance one element at a time Step 3 · Recheck every count Step 4 · Finish with the smallest whole numbers

O last: the right side holds 13 O. Each O₂ supplies 2, so write 13/2 O₂, then double every coefficient.

step equation
C, then H C₄H₁₀ + O₂ → 4 CO₂ + 5 H₂O
O: right side holds 13 C₄H₁₀ + 13/2 O₂ → 4 CO₂ + 5 H₂O
double it 2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
C: 8 = 8 ✓  ·  H: 20 = 20 ✓  ·  O: 26 = 26 ✓
Dr. Karmach

Worked example 4: solution

C₄H₁₀ + O₂ → CO₂ + H₂O  (skeleton)
Step 2 · Balance one element at a time Step 3 · Recheck every count Step 4 · Finish with the smallest whole numbers
step equation
C, then H C₄H₁₀ + O₂ → 4 CO₂ + 5 H₂O
O: right side holds 13 C₄H₁₀ + 13/2 O₂ → 4 CO₂ + 5 H₂O
double it 2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
C: 8 = 8 ✓  ·  H: 20 = 20 ✓  ·  O: 26 = 26 ✓
13 is odd, so no common factor remains. These are already the smallest whole numbers.
Dr. Karmach

Worked example 4: the route

2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
found: C: 8 = 8 ✓  ·  H: 20 = 20 ✓  ·  O: 26 = 26 ✓

C₄H₁₀ first, O₂ last. The free element took the odd count as 13/2, and doubling every coefficient cleared the fraction.
Dr. Karmach

Practice 2: combustion

C₈H₁₀ + O₂ → CO₂ + H₂O  (skeleton)

Xylene, a paint-thinner solvent, burns in air. Balance with smallest whole numbers. What is the sum of all the coefficients?

  1. 35
  2. 24.5
  3. 49
  4. 25
Dr. Karmach

Practice 2: answer C

C₈H₁₀ + 21/2 O₂ → 8 CO₂ + 5 H₂O
C first: 8 CO₂ · H next: 5 H₂O · O last: 8 × 2 + 5 = 21 on the right, so 21/2 O₂
2 C₈H₁₀ + 21 O₂ → 16 CO₂ + 10 H₂O
C: 16 = 16 ✓ · H: 20 = 20 ✓ · O: 42 = 32 + 10 ✓ · sum: 2 + 21 + 16 + 10 = 49 (answer C)

B stopped at the fraction: 1 + 21/2 + 8 + 5 = 24.5, not whole numbers. A doubled only the O₂: 1 + 21 + 8 + 5 = 35, with 42 O on the left against 21 on the right. D rounded 21/2 up to 11: 1 + 11 + 8 + 5 = 25, and 22 O ≠ 21.

A fraction clears only when every coefficient doubles. 21 is odd, so 2, 21, 16, 10 share no factor: 49 is the smallest-whole-number sum.
Dr. Karmach

Practice 3

Al + O₂ → Al₂O₃  (skeleton)
Al: 1 ≠ 2  ·  O: 2 ≠ 3

Aluminum never looks corroded: the fresh metal instantly seals itself under a skin of its own oxide. Balanced with smallest whole numbers, which coefficients are correct, in order?

  1. (2, 3, 2)
  2. (8, 6, 4)
  3. (2, 3/2, 1)
  4. (4, 3, 2)
Dr. Karmach

Practice 3: answer D

4 Al + 3 O₂ → 2 Al₂O₃
Al: 4 = 4 ✓  ·  O: 6 = 6 ✓

O shows 2 on the left and 3 on the right; the common multiple 6 forces 3 O₂ and 2 Al₂O₃, and Al follows with 4. A fixed O but never rechecked Al: 2 ≠ 4. B balances every count, then skips the last step: every coefficient divides by 2. C balances too, but 3/2 is not a whole number; doubling it gives D.

Check: 3 × 2 = 6 O on the left, 2 × 3 = 6 O on the right. Fixing one element forced the next: recheck after every change.
Dr. Karmach

Practice 4

N₂ + H₂ → NH₃  (skeleton)
N: 2 ≠ 1  ·  H: 2 ≠ 3

Ammonia for fertilizer is made from nitrogen pulled straight out of the air. Balance with smallest whole numbers. What is the sum of all the coefficients, counting every unwritten 1?

  1. 3
  2. 5
  3. 6
  4. 12
Dr. Karmach

Practice 4: answer C

N₂ + 3 H₂ → 2 NH₃
N: 2 = 2 ✓  ·  H: 6 = 6 ✓  ·  sum: 1 + 3 + 2 = 6

A read the skeleton as already balanced: 1 + 1 + 1 = 3, but N is 2 ≠ 1. B dropped the unwritten 1 on N₂: 3 + 2 = 5. D doubled every coefficient without reducing: 2 × 6 = 12.

H check: 3 × 2 = 6 on the left, 2 × 3 = 6 on the right ✓. The coefficient nobody writes is the one this question is really about.
Dr. Karmach

Practice 5

Na + H₂O → NaOH + H₂  (skeleton)
Na: 1 = 1  ·  H: 2 ≠ 3  ·  O: 1 = 1

A pea-sized piece of sodium skitters across water, fizzing as it goes. Balanced with smallest whole numbers, which coefficients are correct, in order?

  1. (2, 2, 2, 1)
  2. (1, 1, 1, 1)
  3. (2, 2, 2, 2)
  4. (4, 4, 4, 2)
Dr. Karmach

Practice 5: answer A

2 Na + 2 H₂O → 2 NaOH + H₂
Na: 2 = 2 ✓  ·  H: 4 = 2 + 2 ✓  ·  O: 2 = 2 ✓

H sits in three formulas, so it goes last: set Na and O with matching 2s, and H₂'s coefficient absorbs what remains: (4 - 2)/2 = 1. B leaves H at 2 ≠ 3. C puts a 2 on everything: H becomes 4 ≠ 6. D balances, but every coefficient divides by 2.

The fizzing is the H₂ leaving. The equation is calm; the demo is why sodium is stored under oil instead of water.
Dr. Karmach

Practice 6: from words to an equation

Dinitrogen monoxide gas is used by some dental practitioners as an anesthetic. It is produced by careful heating of solid ammonium nitrate; water vapor is a by-product. Write the balanced chemical equation.

A problem may hand you the formulas, give only the names, or expect a prediction. Here the naming rules supply every formula.

Dr. Karmach

Practice 6: solution

dinitrogen monoxide: N₂O  ·  ammonium nitrate: NH₄NO₃  ·  water: H₂O
molecular prefixes give N₂O  ·  ammonium NH₄⁺ + nitrate NO₃⁻ give NH₄NO₃
NH₄NO₃(s) → N₂O(g) + 2 H₂O(g)
N: 2 = 2 ✓  ·  H: 4 = 4 ✓  ·  O: 3 = 1 + 2 ✓

Names first, then balance. Only H and O need attention, and 2 H₂O settles both at once. The heating is done carefully because ammonium nitrate, heated carelessly, has a second decomposition that is considerably louder.

The equation reads back as the sentence it came from: ammonium nitrate reacts to form dinitrogen monoxide and water. The (g) on the water records the "vapor" in the story.
Dr. Karmach

Check yourself

  1. In 2 Al₂O₃, how many Al atoms in total? Which of the two numbers may change during balancing?
  2. Why is changing a subscript always wrong, even when the counts match?

Balanced equations arrive by the thousand, but their shapes do not: nearly all repeat a handful of patterns, and the pattern predicts the products before any balancing starts.

Dr. Karmach

2 · Types of Reactions

Spot the evidence that a reaction occurred, classify any equation as one of the five reaction types, and predict products from the pattern.

Dr. Karmach

Signs of a new substance

Baking soda and vinegar foam. A nail turns brown and flaky. Stove gas burns blue. Each change makes a new substance, and each leaves a visible sign.

Dr. Karmach

Reactions repeat a few patterns

2 Na + Cl₂ → 2 NaCl
element + element → one compound
2 Mg + O₂ → 2 MgO
element + element → one compound, the same pattern

Millions of reactions are known. Nearly all follow a few repeating patterns, visible in the equation's shape. Recognizing the pattern tells what the products must be before any balancing starts.

Dr. Karmach

Evidence a reaction occurred

New substances have new properties, so the change is visible. Watch for a color change, a gas bubbling out, a solid settling from clear solutions (a precipitate), a temperature change, or light.

Dr. Karmach

Reading a pattern

A + BC → AC + B
each letter stands for an element or an ion, not one particular substance
Zn + 2 HCl → ZnCl₂ + H₂
A = Zn  ·  BC = HCl (B is H, C is Cl)  ·  AC = ZnCl₂  ·  B leaves as H₂

A pattern is a template: any element or ion can play a letter. Coefficients play no part; the pattern reads only which substances are elements and which are compounds.

Dr. Karmach

The five patterns

Five shapes suffice: atoms can only join, split apart, or trade partners. The shape carries the classification: how many substances on each side, element or compound. Combustion adds a signature: O₂ consumed, CO₂ and H₂O formed.

Dr. Karmach

The method

  1. Inventory each side. Count the substances; mark each as element or compound.
  2. Match the shape. Pick the pattern the inventory fits.
  3. Name the type and complete the products. If products are missing, the pattern supplies them.
Dr. Karmach

Worked example 1: heating limestone

Step 1 · Inventory each side

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds  ·  O: 3 = 1 + 2 ✓

Limestone breaks down in a hot kiln. Classify the reaction.

A common first attempt: CO₂ forms, so combustion. Test it.

Dr. Karmach

Worked example 1: solution

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds

A common first attempt

CaCO₃ → CaO + CO₂ as a combustion
combustion: fuel + O₂ → CO₂ + H₂O  ·  no O₂ is consumed here ✗

Nothing burns. Combustion consumes O₂ as a reactant, and no O₂ appears on the left.

Dr. Karmach

Worked example 1: solution

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds
A common first attempt
CaCO₃ → CaO + CO₂ as a combustion
combustion: fuel + O₂ → CO₂ + H₂O  ·  no O₂ is consumed here ✗
Step 2 · Match the shape

One reactant, two products. Only one pattern starts from a single substance: AB → A + B.

Dr. Karmach

Worked example 1: solution

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds
A common first attempt
CaCO₃ → CaO + CO₂ as a combustion
combustion: fuel + O₂ → CO₂ + H₂O  ·  no O₂ is consumed here ✗
Step 2 · Match the shape Step 3 · Name the type and complete the products
CaCO₃(s) → CaO(s) + CO₂(g): decomposition
Ca: 1 = 1 ✓  ·  C: 1 = 1 ✓  ·  O: 3 = 1 + 2 ✓
Dr. Karmach

Worked example 1: solution

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds
A common first attempt
CaCO₃ → CaO + CO₂ as a combustion
combustion: fuel + O₂ → CO₂ + H₂O  ·  no O₂ is consumed here ✗
Step 2 · Match the shape Step 3 · Name the type and complete the products
CaCO₃(s) → CaO(s) + CO₂(g): decomposition
Ca: 1 = 1 ✓  ·  C: 1 = 1 ✓  ·  O: 3 = 1 + 2 ✓
Heat split one compound into two simpler ones. CO₂ appeared without any burning: the products alone cannot name the type.
Dr. Karmach

Worked example 1: the route on the map

CaCO₃(s) → CaO(s) + CO₂(g): decomposition
given: one reactant, a compound · found: decomposition

The first question settles it: one reactant. The CO₂ never reaches the fuel question. ✓
Dr. Karmach

Take-home: combustion is read from the reactants

CH₄ + 2 O₂ → CO₂ + 2 H₂O: combustion
O₂ consumed  ·  a fuel burned to CO₂ and H₂O
CaCO₃ → CaO + CO₂: decomposition
CO₂ formed, but no O₂ consumed: one compound splitting

A product alone never classifies a reaction. Combustion needs O₂ on the reactant side; CO₂ among the products can come from burning or from breaking down.

Dr. Karmach

Worked example 2: propane on a grill

Step 1 · Inventory each side

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂  ·  products not yet written

Propane burns in a grill. Classify the reaction, write the products the pattern requires, and balance.

Dr. Karmach

Worked example 2: solution

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂

Step 2 · Match the shape

A fuel reacting with O₂ fits one pattern: combustion.

Dr. Karmach

Worked example 2: solution

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂
Step 2 · Match the shape Step 3 · Name the type and complete the products
C₃H₈ + O₂ → CO₂ + H₂O  (skeleton)
every C leaves in CO₂  ·  every H leaves in H₂O

The pattern fixes both products before any balancing. Balancing now assigns the coefficients: C first, H second, O last.

Dr. Karmach

Worked example 2: solution

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂
Step 2 · Match the shape Step 3 · Name the type and complete the products
C₃H₈ + O₂ → CO₂ + H₂O  (skeleton)
every C leaves in CO₂  ·  every H leaves in H₂O
The balance check
C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O
C: 3 = 3 ✓  ·  H: 8 = 8 ✓  ·  O: 10 = 6 + 4 ✓
Dr. Karmach

Worked example 2: solution

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂
Step 2 · Match the shape Step 3 · Name the type and complete the products
C₃H₈ + O₂ → CO₂ + H₂O  (skeleton)
every C leaves in CO₂  ·  every H leaves in H₂O
The balance check
C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O
C: 3 = 3 ✓  ·  H: 8 = 8 ✓  ·  O: 10 = 6 + 4 ✓
Every carbon–hydrogen fuel burns to the same two products. The pattern chose CO₂ and H₂O; balancing only chose the amounts.
Dr. Karmach

Worked example 2: the route on the map

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(g): combustion
given: a fuel + O₂ · found: combustion, CO₂ and H₂O

Two reactants, and two products, not one: the first two exits pass. A C, H fuel with O₂ exits at combustion, and that exit fixes CO₂ and H₂O. ✓
Dr. Karmach

Your turn: magnesium in acid

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
bubbles rise as the metal dissolves  ·  H: 2 = 2 ✓  ·  Cl: 2 = 2 ✓
step question answer
1 · Inventory each side element or compound? bare element + compound → compound + bare
2 · Match the shape which pattern fits? A + BC → + B
3 · Name the type displacement

Complete the three steps.

Dr. Karmach

Your turn: magnesium in acid

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
bubbles rise as the metal dissolves  ·  H: 2 = 2 ✓  ·  Cl: 2 = 2 ✓
step question answer
1 · Inventory each side element or compound? bare element + compound → compound + bare
2 · Match the shape which pattern fits? A + BC → + B
3 · Name the type displacement

Complete the three steps.

Mg + 2 HCl → MgCl₂ + H₂: single displacement
Mg displaces hydrogen from HCl  ·  the escaping H₂ gas is the visible evidence
Dr. Karmach

Where this goes wrong

Reading any two-and-two equation as a partner swap. Zn + CuSO₄ → ZnSO₄ + Cu shows two reactants and two products, but Zn enters as a bare element. Double displacement needs two compounds; a bare element displacing another is single displacement.
Calling every CO₂ producer combustion. CaCO₃ → CaO + CO₂ releases CO₂ with no O₂ consumed. Combustion consumes O₂ and forms CO₂ and H₂O; one compound splitting apart is decomposition.
Reading the arrow backwards. Combination builds one product from several reactants; decomposition splits one reactant into several products. 2 HgO → 2 Hg + O₂ starts from a single compound: decomposition.
Calling every bright, hot reaction combustion. 2 Na + Cl₂ → 2 NaCl gives off heat and light, yet no O₂ is consumed and no CO₂ or H₂O forms. Two elements forming one compound: combination.
Dr. Karmach

Practice 1

2 C₂H₂(g) + 5 O₂(g) → 4 CO₂(g) + 2 H₂O(g)
C: 4 = 4 ✓  ·  H: 4 = 4 ✓  ·  O: 10 = 8 + 2 ✓

A welding torch burns acetylene, C₂H₂, in pure oxygen. Which type best classifies this reaction?

  1. Double displacement: two reactants form two products, so two pairs traded partners
  2. Combination: the fuel and the oxygen combine into new compounds
  3. Combustion: a carbon–hydrogen fuel consumes O₂ and forms CO₂ and H₂O
  4. Decomposition: the heat breaks the C₂H₂ molecule apart
Dr. Karmach

Practice 1: answer C

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O: combustion (answer C)
a carbon–hydrogen fuel consumes O₂ and forms CO₂ and H₂O: the full signature

A: a partner swap needs two compounds trading ions, and O₂ is a bare element. B: combination merges everything into one product; two products form here. D: decomposition starts from one reactant; two react here, and the fuel is not falling apart on its own.

Fuel and O₂ on the left, CO₂ and H₂O on the right. The same signature classifies every burning hydrocarbon.
Dr. Karmach

Worked example 3: single or double displacement

Step 1 · Inventory each side

Zn(s) + CuSO₄(aq) → ZnSO₄(aq) + Cu(s)
bare element + compound → compound + bare element
AgNO₃(aq) + KCl(aq) → AgCl(s) + KNO₃(aq)
compound + compound → compound + compound · no bare element

Each equation shows two reactants and two products. Classify each reaction.

Dr. Karmach

Worked example 3: match the shape

Zn + CuSO₄ → ZnSO₄ + Cu
bare element + compound → compound + bare element
AgNO₃ + KCl → AgCl + KNO₃
compound + compound → compound + compound

Step 2 · Match the shape

Counting substances cannot separate these: both show two reactants and two products. The inventory can: the first equation carries a bare element, the second carries none.

Dr. Karmach

Worked example 3: match the shape

Zn + CuSO₄ → ZnSO₄ + Cu
bare element + compound → compound + bare element
AgNO₃ + KCl → AgCl + KNO₃
compound + compound → compound + compound

Step 2 · Match the shape

Counting substances cannot separate these: both show two reactants and two products. The inventory can: the first equation carries a bare element, the second carries none.
The first fits A + BC → AC + B. The second fits AB + CD → AD + CB.

Substance counts match pattern to pattern. The element-or-compound inventory is what tells the two displacements apart.
Dr. Karmach

Worked example 3: name the types

Step 3 · Name the type and complete the products

Zn + CuSO₄ → ZnSO₄ + Cu: single displacement
A + BC → AC + B  ·  Zn displaces Cu; copper leaves as the bare element
Dr. Karmach

Worked example 3: name the types

Step 3 · Name the type and complete the products

Zn + CuSO₄ → ZnSO₄ + Cu: single displacement
A + BC → AC + B  ·  Zn displaces Cu; copper leaves as the bare element
AgNO₃ + KCl → AgCl + KNO₃: double displacement
AB + CD → AD + CB  ·  the compounds trade partners; AgCl is a precipitate
Dr. Karmach

Worked example 3: name the types

Step 3 · Name the type and complete the products

Zn + CuSO₄ → ZnSO₄ + Cu: single displacement
A + BC → AC + B  ·  Zn displaces Cu; copper leaves as the bare element
AgNO₃ + KCl → AgCl + KNO₃: double displacement
AB + CD → AD + CB  ·  the compounds trade partners; AgCl is a precipitate
A bare element among the reactants marks single displacement. Two compounds trading partners, with no bare element anywhere, marks double displacement.
Dr. Karmach

Worked example 3: the route on the map

Zn + CuSO₄ → ZnSO₄ + Cu: single displacement
given: bare element + compound
AgNO₃ + KCl → AgCl + KNO₃: double displacement
given: compound + compound

Both pass the first three questions. The fourth splits them: a bare element exits at single displacement; two compounds run on to double displacement. ✓
Dr. Karmach

Practice 2

Ba(NO₃)₂(aq) + K₂SO₄(aq) → BaSO₄(s) + 2 KNO₃(aq)
two clear solutions mixed; a white solid settles out

Barium nitrate and potassium sulfate solutions are mixed, and a white solid appears. Which type best classifies this reaction?

  1. Single displacement: barium displaces potassium from its compound
  2. Combination: the two reactants combine into the one solid product
  3. Decomposition: a compound broke down, which is why a solid fell out
  4. Double displacement: two compounds trade partners, and one new pair leaves as a solid
Dr. Karmach

Practice 2: answer D

Ba(NO₃)₂ + K₂SO₄ → BaSO₄ + 2 KNO₃: double displacement (answer D)
AB + CD → AD + CB  ·  the new pair BaSO₄ is the precipitate, the visible evidence

A: single displacement needs a bare element among the reactants, and every substance here is a compound. B: combination ends in one product; two form, and KNO₃ stays dissolved. C: decomposition starts from one reactant; two were mixed, and nothing split into simpler substances.

Two compounds in, two compounds out, one of them insoluble. The white solid is the evidence that the partners traded.
Dr. Karmach

Practice 3

2 H₂O₂(aq) → 2 H₂O(l) + O₂(g)
H: 4 = 4 ✓  ·  O: 4 = 2 + 2 ✓

A brown bottle of drugstore peroxide slowly goes flat on the shelf. Which type classifies this reaction?

  1. Combustion: O₂ appears in the equation
  2. Decomposition: one compound splits into two simpler substances
  3. Combination: reading right to left, two substances build into one
  4. Double displacement: two products form, so two pairs traded partners
Dr. Karmach

Practice 3: answer B

2 H₂O₂ → 2 H₂O + O₂: decomposition
one reactant, a compound → two products  ·  no O₂ on the left

A: combustion consumes O₂ as a reactant; here O₂ is produced. C: the arrow reads left to right only; run backwards, the equation describes a different reaction. D: double displacement needs two compounds trading partners, and only one substance reacts.

The bottle goes flat because the peroxide quietly falls apart into water and oxygen. A product's identity never names the type; the reactant side does.
Dr. Karmach

Practice 4

2 K(s) + Cl₂(g) → 2 KCl(s)
K: 2 = 2 ✓  ·  Cl: 2 = 2 ✓

Potassium metal meets chlorine gas with a violent flash of heat and light. Which type classifies this reaction?

  1. Combustion: it is bright and hot, exactly like a flame
  2. Double displacement: potassium and chlorine trade partners
  3. Decomposition: the Cl₂ molecule splits apart as it reacts
  4. Combination: two elements form one compound
Dr. Karmach

Practice 4: answer D

2 K + Cl₂ → 2 KCl: combination
element + element → one compound  ·  no O₂ consumed, no CO₂ or H₂O formed

A: bright and hot describes the energy released, not the type; combustion consumes O₂, and none appears here. B: a partner swap needs two compounds, and both reactants are bare elements. C: Cl₂'s bond does break, but the shape reads whole substances: one compound is built, and nothing splits into simpler substances.

Same lesson as 2 Na + Cl₂: drama is not a classification. The shape is: two elements in, one compound out.
Dr. Karmach

Practice 5

Fe(s) + CuSO₄(aq) → FeSO₄(aq) + Cu(s)
an iron nail left in blue copper sulfate solution turns copper-colored

Which type classifies this reaction?

  1. Double displacement: two compounds appear, so two pairs traded partners
  2. Single displacement: a bare element displaces copper from its compound
  3. Combination: the iron and the copper sulfate combine
  4. Decomposition: CuSO₄ breaks down and leaves copper behind
Dr. Karmach

Practice 5: answer B

Fe + CuSO₄ → FeSO₄ + Cu: single displacement
bare element + compound → compound + bare element  ·  Fe: 1 = 1 ✓  ·  Cu: 1 = 1 ✓

A: double displacement needs two compounds and no bare element; Fe enters bare and Cu leaves bare. C: combination ends in one product, and two form here. D: decomposition starts from a single reactant splitting on its own; here iron does the pushing.

The copper color plating onto the nail is the displaced element itself. One compound on each side plus a bare element: the single displacement signature.
Dr. Karmach

Two ways to classify the same reaction

sort by shape: combination · decomposition · single displacement · double displacement
how many pieces, element or compound, and how they recombine
sort by driver: precipitation · acid base · redox · combustion
what pushes the reaction forward
AgNO₃ + KCl → AgCl + KNO₃ · shape: double displacement · driver: precipitation
Zn + CuSO₄ → ZnSO₄ + Cu · shape: single displacement · driver: redox

One reaction, a name from each scheme. Double displacement splits by driver into precipitation and neutralization; single displacement and combustion are both redox.

Dr. Karmach

Practice 6: both lenses

Mg(s) + 2 AgNO₃(aq) → Mg(NO₃)₂(aq) + 2 Ag(s)
a clear solution · a gray-white solid collects on the ribbon

Magnesium ribbon stands in silver nitrate solution, and a solid builds up on it. Classify this reaction once per scheme. Which pair of names is correct?

  1. Double displacement, and a precipitation
  2. Single displacement, and a precipitation
  3. Double displacement, and a redox
  4. Single displacement, and a redox
Dr. Karmach

Practice 6: answer D

Mg + 2 AgNO₃ → Mg(NO₃)₂ + 2 Ag: single displacement, and a redox (answer D)
bare element + compound → compound + bare element  ·  Mg: 1 = 1 ✓  ·  Ag: 2 = 2 ✓  ·  N: 2 = 2 ✓  ·  O: 6 = 6 ✓

A took both names from the surface: a solid appeared, and two substances went in and two came out. B has the shape right, but the solid is silver metal pushed out of its compound, not a new ion pair leaving the water; precipitation belongs to double displacement. C has the driver right, but Mg enters as a bare element, and a partner swap needs two compounds. Single displacement is driven by electron transfer: a redox.

A solid appearing is not proof of a precipitate. Ask what the solid is: a new ion pairing, or an element pushed out of its compound.
Dr. Karmach

Check yourself

  1. Electrolysis splits water: 2 H₂O → 2 H₂ + O₂. Inventory each side and name the type. O₂ appears as a product: why is this not combustion?
  2. Butane, C₄H₁₀, burns in a lighter. Write the two products before balancing anything. Which pattern makes that prediction possible?

A double displacement happens only when a new pair leaves the solution: as a solid, a gas, or water. The solubility rules predict which ion pairs drop out as precipitates.

Dr. Karmach

3 · Solubility Rules & Precipitation

Predict whether mixing two solutions makes a precipitate: swap the partners, check each new compound against the solubility rules, and write the balanced equation with states.

Dr. Karmach

A solid from two clear liquids

Two beakers, two clear liquids. Poured together, they instantly cloud, and a bright yellow solid settles to the bottom. No solid went in.

Dr. Karmach

What dissolving looks like

Dissolving an ionic solid means the ions separate and travel independently. The solid's Na⁺ and Cl⁻ leave the stack one ion at a time and spread through the water.

Dr. Karmach

Soluble or insoluble

NaCl(aq) is soluble: it dissolves, and its ions spread through the water
(aq) = aqueous, dissolved in water
AgCl(s) is insoluble: it stays a solid
(s) = solid; it does not dissolve

An ionic compound in water dissolves or it does not. Dissolving is a tug-of-war: water pulls the ions apart, and for a few pairings the ion-ion attraction wins, so the compound stays solid.

Dr. Karmach

Check the always-soluble ions first

group 1 cations (Li⁺, Na⁺, K⁺, ...) · NH₄⁺ · NO₃⁻
compounds of these never precipitate · any new pairing holding one stays (aq)

Three families never precipitate. Check a new pairing against this short list first; it settles most cases. Only a pairing with none of the three needs the chart's exception lines.

Dr. Karmach

The solubility rules

NAGSAG: Nitrates · Acetates · Group 1 · Sulfates · Ammonium · Group 17 halides
the mostly-soluble families · only the sulfates and the halides (Cl⁻ Br⁻ I⁻) carry exception lists

One line decides each compound: read its ions, find their line, apply the exception list.

Dr. Karmach

Mixing two solutions: the partners swap

Dissolved compounds are separated ions. Mixing two solutions lets each cation meet the other anion. A new pairing the rules call insoluble forms a solid: a precipitate.

Dr. Karmach

Warm-up: formulas from charge balance

Ba²⁺ + OH⁻ → ? · Al³⁺ + SO₄²⁻ → ?
wanted: the neutral formula each ion pair builds
ions charge balance formula
Ba²⁺ + OH⁻ 1(2+) + 2(1−) = 0 Ba(OH)
Al³⁺ + SO₄²⁻ 2(3+) + 3(2−) = 0

Complete both formulas.

Dr. Karmach

Warm-up: formulas from charge balance

Ba²⁺ + OH⁻ → ? · Al³⁺ + SO₄²⁻ → ?
wanted: the neutral formula each ion pair builds
ions charge balance formula
Ba²⁺ + OH⁻ 1(2+) + 2(1−) = 0 Ba(OH)
Al³⁺ + SO₄²⁻ 2(3+) + 3(2−) = 0

Complete both formulas.

Ba(OH)₂ · Al₂(SO₄)₃
1(2+) + 2(1−) = 0 ✓ · 2(3+) + 3(2−) = 0 ✓ · charge balance sets the subscripts, exactly as when naming ionic compounds
Dr. Karmach

The method

  1. Swap the partners. New cation–anion pairs.
  2. Build each new formula. Charge balance sets subscripts.
  3. Check each product against the rules. Soluble → (aq); insoluble → (s).
  4. Write the balanced equation with states. Both products (aq): no reaction.
Dr. Karmach

Worked example 1: soluble or insoluble

CaCO₃ · K₂CO₃
wanted: the state of each in water, (aq) or (s)

White marble is CaCO₃. Potash fertilizer, K₂CO₃, is spread as a clear solution. Assign each compound its state in water.

Dr. Karmach

Worked example 1: solution

CaCO₃ · K₂CO₃
wanted: the state of each in water, (aq) or (s)

Read the ions

CaCO₃ = Ca²⁺ + CO₃²⁻ · K₂CO₃ = 2 K⁺ + CO₃²⁻
both compounds are carbonates: the carbonate line decides both
Dr. Karmach

Worked example 1: solution

CaCO₃ · K₂CO₃
wanted: the state of each in water, (aq) or (s)
Read the ions
CaCO₃ = Ca²⁺ + CO₃²⁻ · K₂CO₃ = 2 K⁺ + CO₃²⁻
both compounds are carbonates: the carbonate line decides both
Apply the carbonate line

Carbonates are insoluble except with group 1 cations or NH₄⁺.

CaCO₃ → CaCO₃(s) · K₂CO₃ → K₂CO₃(aq)
Ca²⁺: not on the exception list → solid · K⁺: group 1 → the exception applies, dissolved
Dr. Karmach

Worked example 1: solution

CaCO₃ · K₂CO₃
wanted: the state of each in water, (aq) or (s)
Read the ions
CaCO₃ = Ca²⁺ + CO₃²⁻ · K₂CO₃ = 2 K⁺ + CO₃²⁻
both compounds are carbonates: the carbonate line decides both
Apply the carbonate line

Carbonates are insoluble except with group 1 cations or NH₄⁺.

CaCO₃ → CaCO₃(s) · K₂CO₃ → K₂CO₃(aq)
Ca²⁺: not on the exception list → solid · K⁺: group 1 → the exception applies, dissolved
Same anion, opposite states. A rule reads the pair of ions; the exception list is part of the rule.
Dr. Karmach

Worked example 1: the route on the chart

CaCO₃ · K₂CO₃
found: CaCO₃(s) · K₂CO₃(aq)

Both compounds read the carbonate line: insoluble. K⁺ is group 1, an EXCEPT partner, so K₂CO₃ flips to (aq). Ca²⁺ is not on the list: CaCO₃(s).
Dr. Karmach

Worked example 2: AgNO₃ + NaCl

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

Silver nitrate solution meets salt solution in photographic processing. Both are clear and colorless; mixing them turns the beaker milky white. Predict the solid.

A common first attempt: check AgNO₃ and NaCl against the rules: both soluble, so no solid should form. Test it.

Dr. Karmach

Worked example 2: testing the first attempt

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

A common first attempt

AgNO₃ soluble ✓ · NaCl soluble ✓ → no solid?
nitrates: always soluble · group 1: always soluble, yet the mixture turns white ✗
Dr. Karmach

Worked example 2: testing the first attempt

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

A common first attempt

AgNO₃ soluble ✓ · NaCl soluble ✓ → no solid?
nitrates: always soluble · group 1: always soluble, yet the mixture turns white ✗
Both reactants pass the rules. That is what (aq) already records: they arrived dissolved. The white solid must be a compound neither beaker held.
The mixed beaker holds four ions moving independently: Ag⁺, NO₃⁻, Na⁺, Cl⁻. Two of them meet here for the first time.
Dr. Karmach

Worked example 2: the swap

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

Step 1 · Swap the partners Step 2 · Build each new formula

Ag⁺ pairs with Cl⁻; Na⁺ pairs with NO₃⁻. Both new pairs balance one-to-one.

Dr. Karmach

Worked example 2: the swap

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

Step 1 · Swap the partners Step 2 · Build each new formula

Ag⁺ pairs with Cl⁻; Na⁺ pairs with NO₃⁻. Both new pairs balance one-to-one.

new pairs: AgCl and NaNO₃
AgCl: 1(+1) + 1(−1) = 0 ✓ · NaNO₃: 1(+1) + 1(−1) = 0 ✓
Two dissolved compounds went in; two new pairings remain to be checked against the rules.
Dr. Karmach

Worked example 2: states and the equation

AgNO₃(aq) + NaCl(aq) → AgCl + NaNO₃
new pairs built · wanted: each product's state

Step 3 · Check each product against the rules

AgCl → (s) · NaNO₃ → (aq)
chlorides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺; Ag⁺ is on the list · nitrates: always soluble
Dr. Karmach

Worked example 2: states and the equation

AgNO₃(aq) + NaCl(aq) → AgCl + NaNO₃
new pairs built · wanted: each product's state
Step 3 · Check each product against the rules
AgCl → (s) · NaNO₃ → (aq)
chlorides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺; Ag⁺ is on the list · nitrates: always soluble
Step 4 · Write the balanced equation with states
AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
Ag: 1 = 1 · NO₃: 1 = 1 · Na: 1 = 1 · Cl: 1 = 1 · balanced as written
Dr. Karmach

Worked example 2: states and the equation

AgNO₃(aq) + NaCl(aq) → AgCl + NaNO₃
new pairs built · wanted: each product's state
Step 3 · Check each product against the rules
AgCl → (s) · NaNO₃ → (aq)
chlorides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺; Ag⁺ is on the list · nitrates: always soluble
Step 4 · Write the balanced equation with states
AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
Ag: 1 = 1 · NO₃: 1 = 1 · Na: 1 = 1 · Cl: 1 = 1 · balanced as written
The milky white is AgCl, the one new pairing the rules call insoluble. Na⁺ and NO₃⁻ never left the water.
Dr. Karmach

Worked example 2: the route on the chart

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
found: AgCl(s) · NaNO₃(aq)

NaNO₃ reads the nitrate line: always soluble. AgCl reads the chloride line, and Ag⁺ is an EXCEPT partner: the verdict flips to (s).
Dr. Karmach

Take-home: apply the rules to the products

AgNO₃(aq) + NaCl(aq): reactants already dissolved
(aq) on a reactant records that it already dissolved
Ag⁺ + Cl⁻ → AgCl(s): the new pairing
chlorides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺

Swap first, then check. The precipitate question is about the two new pairings, never about the compounds that arrived dissolved.

Dr. Karmach

Your turn: Pb(NO₃)₂ + KI

Pb(NO₃)₂(aq) + KI(aq) → ?
two clear solutions · mixing makes a bright yellow solid
step question answer
1 · swap the partners which new pairs form? Pb²⁺ with I⁻ · K⁺ with NO₃⁻
2 · build each new formula 1(2+) + 2(1−) = 0 PbI and KNO₃
3 · check each product which lines of the rules? PbI₂ → () · KNO₃ → ()
4 · write the balanced equation coefficients

Complete the prediction.

Dr. Karmach

Your turn: Pb(NO₃)₂ + KI

Pb(NO₃)₂(aq) + KI(aq) → ?
two clear solutions · mixing makes a bright yellow solid
step question answer
1 · swap the partners which new pairs form? Pb²⁺ with I⁻ · K⁺ with NO₃⁻
2 · build each new formula 1(2+) + 2(1−) = 0 PbI and KNO₃
3 · check each product which lines of the rules? PbI₂ → () · KNO₃ → ()
4 · write the balanced equation coefficients

Complete the prediction.

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
PbI₂: 1(2+) + 2(1−) = 0 ✓ · iodides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺ · nitrates: always soluble · PbI₂ settles brilliant yellow
Dr. Karmach

Where this goes wrong

Checking the rules on the starting solutions. AgNO₃ and NaCl both pass: they were already dissolved. The rules judge the products of the swap: Ag⁺ with Cl⁻ gives AgCl, and the chloride line puts Ag⁺ on its exception list.
Calling the soluble product the precipitate. BaCl₂ + Na₂SO₄ gives two new pairs. NaCl passes the rules, so its ions stay dissolved. The solid is the pairing that does not: BaSO₄.
Expecting a starting compound to fall out. A compound that arrived dissolved stays dissolved. The precipitate is always a new pairing: ions that arrived in different beakers.
Dragging old subscripts into new formulas. Pb(NO₃)₂ + KI: copying KI's one-to-one ratio gives PbI, and 1(+2) + 1(−1) = +1, not neutral. Charge balance builds the new formula: PbI₂, 1(+2) + 2(−1) = 0.
Dr. Karmach

Practice 1

AgNO₃(aq) + Na₂S(aq) → ?
two clear solutions are mixed

Silver nitrate solution is poured into sodium sulfide solution. Which precipitate forms, if any?

  1. Ag₂S
  2. NaNO₃
  3. AgS
  4. No precipitate: both new pairings stay dissolved
Dr. Karmach

Practice 1: answer A

2 AgNO₃(aq) + Na₂S(aq) → Ag₂S(s) + 2 NaNO₃(aq) (answer A)
sulfides: insoluble except group 1 and NH₄⁺ · Ag₂S: 2(1+) + 1(2−) = 0 ✓ · Ag: 2 = 2 · S: 1 = 1 · Na: 2 = 2 · NO₃: 2 = 2

B is the soluble product: sodium is group 1 and nitrate is always soluble, so NaNO₃'s ions stay dissolved. C has the right pairing and the wrong formula: AgS gives 1(1+) + 1(2−) = −1, so charge balance needs two Ag⁺ per S²⁻. D skipped the sulfide line: Ag⁺ is not group 1 or NH₄⁺, so Ag₂S falls out.

Of the four ions mixed, only Ag⁺ + S²⁻ lands on an insoluble line. One insoluble pairing, one solid: black Ag₂S, the same compound that tarnishes silverware.
Dr. Karmach

Worked example 3: BaCl₂ + NaOH

BaCl₂(aq) + NaOH(aq) → ?
wanted: the precipitate, if one forms

Solutions of barium chloride and sodium hydroxide are mixed. Work all four steps.

Dr. Karmach

Worked example 3: the swap

BaCl₂(aq) + NaOH(aq) → ?
wanted: the precipitate, if one forms

Step 1 · Swap the partners Step 2 · Build each new formula

Ba²⁺ pairs with OH⁻; Na⁺ pairs with Cl⁻. Ba²⁺ needs two OH⁻ to reach zero charge.

Dr. Karmach

Worked example 3: the swap

BaCl₂(aq) + NaOH(aq) → ?
wanted: the precipitate, if one forms

Step 1 · Swap the partners Step 2 · Build each new formula

Ba²⁺ pairs with OH⁻; Na⁺ pairs with Cl⁻. Ba²⁺ needs two OH⁻ to reach zero charge.

new pairs: Ba(OH)₂ and NaCl
Ba(OH)₂: 1(+2) + 2(−1) = 0 ✓ · NaCl: 1(+1) + 1(−1) = 0 ✓
The new formulas come from charge balance, never from the reactants' subscripts.
Dr. Karmach

Worked example 3: solution

BaCl₂(aq) + NaOH(aq) → Ba(OH)₂ + NaCl
new pairs built · wanted: each product's state

Step 3 · Check each product against the rules

Most hydroxides are insoluble. The exception list is part of the rule, and Ba²⁺ is on it.

Ba(OH)₂ → (aq) · NaCl → (aq)
hydroxides: insoluble except group 1 and Ba²⁺ · group 1: always soluble
Dr. Karmach

Worked example 3: solution

BaCl₂(aq) + NaOH(aq) → Ba(OH)₂ + NaCl
new pairs built · wanted: each product's state
Step 3 · Check each product against the rules
Ba(OH)₂ → (aq) · NaCl → (aq)
hydroxides: insoluble except group 1 and Ba²⁺ · group 1: always soluble
Step 4 · Write the balanced equation with states
BaCl₂(aq) + NaOH(aq) → no reaction
both new pairings stay dissolved: nothing leaves the solution
Dr. Karmach

Worked example 3: solution

BaCl₂(aq) + NaOH(aq) → Ba(OH)₂ + NaCl
new pairs built · wanted: each product's state
Step 3 · Check each product against the rules
Ba(OH)₂ → (aq) · NaCl → (aq)
hydroxides: insoluble except group 1 and Ba²⁺ · group 1: always soluble
Step 4 · Write the balanced equation with states
BaCl₂(aq) + NaOH(aq) → no reaction
both new pairings stay dissolved: nothing leaves the solution
The mixed beaker stays clear: it holds four kinds of dissolved ions. A precipitate needs one insoluble pairing, and here there is none.
Dr. Karmach

Worked example 3: the route on the chart

BaCl₂(aq) + NaOH(aq) → no reaction
found: Ba(OH)₂(aq) · NaCl(aq)

NaCl reads the group 1 line: always soluble. Ba²⁺ is an EXCEPT partner on the hydroxide line, so Ba(OH)₂ flips to (aq). Two teal verdicts: nothing leaves the solution.
Dr. Karmach

Practice 2

four beakers · one pair of clear solutions mixed in each
three beakers turn cloudy · wanted: the mixture that stays clear

Which mixture stays clear?

  1. Pb(NO₃)₂ + NH₄Cl
  2. SrCl₂ + Li₂SO₄
  3. Ba(NO₃)₂ + NaI
  4. NiCl₂ + (NH₄)₂CO₃
Dr. Karmach

Practice 2: answer C

new pairs: BaI₂ → (aq) · NaNO₃ → (aq) → no reaction (answer C)
BaI₂: 1(+2) + 2(−1) = 0 ✓ · iodides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺ · Ba²⁺ sits on the sulfate list, not the iodide list
A: PbCl₂(s) · B: SrSO₄(s) · D: NiCO₃(s)
Pb²⁺: a chloride exception · Sr²⁺: a sulfate exception · Ni²⁺: not group 1, not NH₄⁺ · each partner (NH₄NO₃, LiCl, NH₄Cl) stays (aq)

A trusted the always-soluble ions: NH₄⁺ and NO₃⁻ stay dissolved, but the new pair PbCl₂ is on the chloride exception list. B remembered only barium on the sulfate list; Sr²⁺ is there too. D applied the ammonium exception to the wrong pairing: (NH₄)₂CO₃ arrived dissolved, but NiCO₃ has no exception.

Barium fails the sulfate line and passes the halide lines. An exception list belongs to one anion: no cation precipitates with everything.
Dr. Karmach

Practice 3

Na₂CO₃(aq) + CaCl₂(aq) → ?
two clear solutions are mixed · the beaker turns cloudy white

Washing soda and calcium chloride road salt, both dissolved. Which precipitate forms, if any?

  1. CaCO₃
  2. NaCl
  3. Na₂CO₃
  4. No precipitate: both new pairings stay dissolved
Dr. Karmach

Practice 3: answer A

Na₂CO₃(aq) + CaCl₂(aq) → CaCO₃(s) + 2 NaCl(aq) (answer A)
carbonates: insoluble except group 1 and NH₄⁺ · CaCO₃: 1(2+) + 1(2−) = 0 ✓ · Na: 2 = 2 · Cl: 2 = 2

B stays dissolved: sodium is group 1, and Ca²⁺ is not on the chloride exception list. C is a reactant: it arrived dissolved, and its ions stay until a new pairing removes them. D skipped the carbonate line: Ca²⁺ is not a group 1 cation, so CaCO₃ falls out.

The always-soluble list clears NaCl instantly: Na⁺ is group 1. Only the Ca²⁺ + CO₃²⁻ pairing needed the chart.
Dr. Karmach

Practice 4

NH₄Cl(aq) + KNO₃(aq) → ?
two clear solutions are mixed

Ammonium chloride and potassium nitrate, both dissolved. Which precipitate forms, if any?

  1. NH₄NO₃
  2. KCl
  3. No precipitate: both new pairings stay dissolved
  4. NH₄Cl
Dr. Karmach

Practice 4: answer C

new pairs: NH₄NO₃ → (aq) · KCl → (aq) → no reaction (answer C)
NH₄NO₃: 1(1+) + 1(1−) = 0 ✓ · KCl: 1(1+) + 1(1−) = 0 ✓ · every ion here sits on the always-soluble list

A pairs ammonium with nitrate: both always soluble, so NH₄NO₃ stays dissolved. B holds K⁺, a group 1 cation: always soluble. D is a reactant that arrived dissolved.

All four ions are on the always-soluble list, so no chart line was ever needed. Four ions went in; all four stay dissolved.
Dr. Karmach

Drill: assign each state

AgBr · K₃PO₄ · PbSO₄ · MgCO₃
wanted: (aq) or (s) for each compound in water
compound the line that decides state
AgBr bromides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺ ()
K₃PO₄ group 1: always soluble ()
PbSO₄ sulfates: soluble except Ba²⁺, Sr²⁺, Pb²⁺ ()
MgCO₃ carbonates: insoluble except group 1, NH₄⁺ ()

Assign each state.

Dr. Karmach

Drill: assign each state

AgBr · K₃PO₄ · PbSO₄ · MgCO₃
wanted: (aq) or (s) for each compound in water
compound the line that decides state
AgBr bromides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺ ()
K₃PO₄ group 1: always soluble ()
PbSO₄ sulfates: soluble except Ba²⁺, Sr²⁺, Pb²⁺ ()
MgCO₃ carbonates: insoluble except group 1, NH₄⁺ ()

Assign each state.

AgBr(s) · K₃PO₄(aq) · PbSO₄(s) · MgCO₃(s)
only K₃PO₄ carries an always-soluble ion · the other three land on exception lists or insoluble families
Dr. Karmach

Check yourself

  1. Solutions of Pb(NO₃)₂ and Na₂SO₄ are mixed. Swap the partners, build both formulas, check each against the rules: which product is the solid?
  2. Solutions of KCl and NH₄NO₃ are mixed. Both new pairings pass the rules. What is the prediction, and why?

Every (aq) compound in a precipitate equation is really separated ions in the water. Writing the dissolved compounds as their ions, then removing the ions that never change, leaves the net ionic equation: the precipitate-forming ions alone.

Dr. Karmach

4 · Net Ionic Equations

Write the molecular, complete ionic, and net ionic equations for a reaction in solution, cancel the spectator ions, and check that the result balances in atoms and charge.

Dr. Karmach

The solid takes only two kinds of particles

Two clear solutions are mixed; a white solid settles. Most dissolved particles are still floating afterward, unchanged. Only two kinds left the water.

Dr. Karmach

Dissolved means separated into ions

A soluble ionic compound does not dissolve as molecules. It exists in the water as separated ions. Writing the ions shows which of them react and which never change.

Dr. Karmach

Three views of the same reaction

The molecular equation lists whole compounds. The two ionic views show what the water actually holds.

"Molecular equation" means written as whole formulas; most compounds in these equations are ionic.
Dr. Karmach

Spectator ions

A spectator ion appears identical on both sides. Cancel the spectators; what remains is the net ionic equation. Any soluble silver salt plus any soluble chloride gives this same net line.

Dr. Karmach

What separates on the page

written as separated ions: only solutes that separate completely in water
the soluble ionic compounds · the few acids that ionize fully, the strong acids
kept whole: everything else
acids that barely ionize: HC₂H₃O₂(aq) stays whole · insoluble solids: AgCl(s) stays intact · covalent molecules: H₂O(l) and sugar

A formula earns ion notation only by existing in the water fully separated. In these reactions that means the soluble salts and the strong acids; everything else keeps its formula whole.

Dr. Karmach

The method

  1. Write the molecular equation with states.
  2. Write each (aq) compound as its ions. Keep charges and coefficients; polyatomic ions stay whole; (s) stays intact.
  3. Cancel the spectator ions.
  4. Check atoms and charge. Both must balance.
Dr. Karmach

Worked example 1: silver chloride

Step 1 · Write the molecular equation with states

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
states from the solubility rules: AgCl insoluble, the rest soluble

A drop of silver nitrate turns salty water cloudy white, a standard test for chloride. Write the complete ionic equation, then the net ionic equation.

Dr. Karmach

Worked example 1: the complete ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular · states from the solubility rules

Step 2 · Write each (aq) compound as its ions

Each (aq) compound separates. The solid does not.

Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
complete ionic · charge: left 1(+1) + 1(−1) + 1(+1) + 1(−1) = 0 · right 0 + 1(+1) + 1(−1) = 0 ✓
Dr. Karmach

Worked example 1: the complete ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular · states from the solubility rules
Step 2 · Write each (aq) compound as its ions
Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
complete ionic · charge: left 1(+1) + 1(−1) + 1(+1) + 1(−1) = 0 · right 0 + 1(+1) + 1(−1) = 0 ✓
Step 3 · Cancel the spectator ions

Na⁺ and NO₃⁻ appear identical on both sides. They never reacted.

Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
spectators: Na⁺ and NO₃⁻
Dr. Karmach

Worked example 1: the complete ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular · states from the solubility rules
Step 2 · Write each (aq) compound as its ions
Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
complete ionic · charge: left 1(+1) + 1(−1) + 1(+1) + 1(−1) = 0 · right 0 + 1(+1) + 1(−1) = 0 ✓
Step 3 · Cancel the spectator ions
Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
spectators: Na⁺ and NO₃⁻
The compound formulas are gone; the water's actual contents are on the page, and the two ions that never react are struck out.
Dr. Karmach

Worked example 1: the net ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular · spectators already cancelled: Na⁺ and NO₃⁻

Step 4 · Check atoms and charge

Only the ions that build the solid remain.

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
net ionic · atoms: Ag 1 = 1 ✓ · Cl 1 = 1 ✓ · charge: left 1(+1) + 1(−1) = 0, right 0 ✓
Dr. Karmach

Worked example 1: the net ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular · spectators already cancelled: Na⁺ and NO₃⁻
Step 4 · Check atoms and charge
Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
net ionic · atoms: Ag 1 = 1 ✓ · Cl 1 = 1 ✓ · charge: left 1(+1) + 1(−1) = 0, right 0 ✓
The net ionic equation balances twice: every atom matches, and both sides carry zero total charge.
Dr. Karmach

Worked example 1: the route on the strip

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
split: AgNO₃, NaCl, NaNO₃ · kept whole: AgCl(s) · found: Ag⁺(aq) + Cl⁻(aq) → AgCl(s)

Three formulas took the yes branch; the solid took no. Na⁺ and NO₃⁻ cancel, and the ions that build AgCl are all that is left. ✓
Dr. Karmach

Worked example 2: lead iodide

Step 1 · Write the molecular equation with states

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
PbI₂ insoluble: the yellow solid of the golden-rain demonstration

Write the complete ionic equation, then the net ionic equation.

A common first attempt for the net: Pb²⁺(aq) + I⁻(aq) → PbI₂(s). Test it.

Dr. Karmach

Worked example 2: the complete ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · PbI₂ is the solid

Step 2 · Write each (aq) compound as its ions

Pb(NO₃)₂ separates into one Pb²⁺ and two whole NO₃⁻. The coefficient on 2 KI carries through: 2 K⁺ and 2 I⁻.

Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
charge: left 1(+2) + 2(−1) + 2(+1) + 2(−1) = 0 · right 0 + 2(+1) + 2(−1) = 0 ✓
Dr. Karmach

Worked example 2: the complete ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · PbI₂ is the solid
Step 2 · Write each (aq) compound as its ions
Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
charge: left 1(+2) + 2(−1) + 2(+1) + 2(−1) = 0 · right 0 + 2(+1) + 2(−1) = 0 ✓
Step 3 · Cancel the spectator ions
Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
spectators: K⁺ and NO₃⁻ · Pb²⁺ and 2 I⁻ have no match to cancel
Dr. Karmach

Worked example 2: the complete ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · PbI₂ is the solid
Step 2 · Write each (aq) compound as its ions
Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
charge: left 1(+2) + 2(−1) + 2(+1) + 2(−1) = 0 · right 0 + 2(+1) + 2(−1) = 0 ✓
Step 3 · Cancel the spectator ions
Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
spectators: K⁺ and NO₃⁻ · Pb²⁺ and 2 I⁻ have no match to cancel
Nitrate separates and cancels as one whole unit, never as N and O pieces, and its coefficient 2 stays with it.
Dr. Karmach

Worked example 2: the net ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · spectators already cancelled: K⁺ and NO₃⁻

A common first attempt

Pb²⁺(aq) + I⁻(aq) → PbI₂(s)
atoms: I 1 ≠ 2 ✗ · charge: left 1(+2) + 1(−1) = +1, right 0 ✗

The coefficient on I⁻ was dropped. Two iodides build each PbI₂.

Dr. Karmach

Worked example 2: the net ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · spectators already cancelled: K⁺ and NO₃⁻
A common first attempt
Pb²⁺(aq) + I⁻(aq) → PbI₂(s)
atoms: I 1 ≠ 2 ✗ · charge: left 1(+2) + 1(−1) = +1, right 0 ✗
Step 4 · Check atoms and charge
Pb²⁺(aq) + 2 I⁻(aq) → PbI₂(s)
atoms: Pb 1 = 1 ✓ · I 2 = 2 ✓ · charge: left 1(+2) + 2(−1) = 0, right 0 ✓
Dr. Karmach

Worked example 2: the net ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · spectators already cancelled: K⁺ and NO₃⁻
A common first attempt
Pb²⁺(aq) + I⁻(aq) → PbI₂(s)
atoms: I 1 ≠ 2 ✗ · charge: left 1(+2) + 1(−1) = +1, right 0 ✗
Step 4 · Check atoms and charge
Pb²⁺(aq) + 2 I⁻(aq) → PbI₂(s)
atoms: Pb 1 = 1 ✓ · I 2 = 2 ✓ · charge: left 1(+2) + 2(−1) = 0, right 0 ✓
The solid is neutral, so the ions that build it must sum to zero. Keeping the coefficients is what makes both checks pass.
Dr. Karmach

Worked example 2: the route on the strip

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
split: Pb(NO₃)₂, KI, KNO₃ · kept whole: PbI₂(s) · found: Pb²⁺(aq) + 2 I⁻(aq) → PbI₂(s)

Same route as silver chloride: the solid took the no branch. K⁺ and NO₃⁻ cancel; Pb²⁺ and 2 I⁻ are left, with their coefficient. ✓
Dr. Karmach

Your turn: barium sulfate

BaCl₂(aq) + Na₂SO₄(aq) → BaSO₄(s) + 2 NaCl(aq)
Step 1 done · BaSO₄ insoluble: the X-ray contrast a patient drinks
step your work
2 · write each (aq) compound as its ions Ba²⁺ + 2 Cl⁻ + 2 Na⁺ + → BaSO₄(s) + 2 Na⁺ + 2 Cl⁻
3 · cancel the spectator ions and
4 · check atoms and charge net: · left charge = right charge 0

Complete steps 2 through 4.

Dr. Karmach

Your turn: barium sulfate

BaCl₂(aq) + Na₂SO₄(aq) → BaSO₄(s) + 2 NaCl(aq)
Step 1 done · BaSO₄ insoluble: the X-ray contrast a patient drinks
step your work
2 · write each (aq) compound as its ions Ba²⁺ + 2 Cl⁻ + 2 Na⁺ + → BaSO₄(s) + 2 Na⁺ + 2 Cl⁻
3 · cancel the spectator ions and
4 · check atoms and charge net: · left charge = right charge 0

Complete steps 2 through 4.

Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s)
spectators: Na⁺, Cl⁻ · atoms: Ba 1 = 1 ✓ · S 1 = 1 ✓ · O 4 = 4 ✓ · charge: left 1(+2) + 1(−2) = 0, right 0 ✓
Sulfate stayed whole from the first line to the last. Its charge comes from the memorized list, and the charge check depends on it.
Dr. Karmach

Where this goes wrong

Splitting the solid into ions. Writing AgCl(s) as Ag⁺(aq) + Cl⁻(aq) lets every ion cancel, and the equation claims nothing happened. A solid formed. Only (aq) compounds separate; (s) stays intact.
Breaking up a polyatomic ion. Dissolved nitrate is NO₃⁻(aq), one whole unit with one charge. Cancel nitrate as nitrate, never as separate N and O.
Dropping the charges. Ag(aq) + Cl(aq) → AgCl(s) shows neutral atoms the water does not contain. Without charges, the charge check cannot be run.
Stopping at the complete ionic equation. If K⁺ and NO₃⁻ still stand on both sides, nothing has been cancelled. The net ionic equation keeps only the ions that build the solid.
Dr. Karmach

Practice 1

SrCl₂(aq) + Na₂CO₃(aq) → SrCO₃(s) + 2 NaCl(aq)
molecular · SrCO₃ is the precipitate

Strontium salts color fireworks red. Aqueous SrCl₂ and Na₂CO₃ are mixed, and SrCO₃ precipitates. Which is the correct net ionic equation?

  1. SrCl₂(aq) + Na₂CO₃(aq) → SrCO₃(s) + 2 NaCl(aq)
  2. Sr²⁺(aq) + 2 Cl⁻(aq) + 2 Na⁺(aq) + CO₃²⁻(aq) → SrCO₃(s) + 2 Na⁺(aq) + 2 Cl⁻(aq)
  3. Sr²⁺(aq) + CO₃²⁻(aq) → SrCO₃(s)
  4. Sr⁺(aq) + CO₃⁻(aq) → SrCO₃(s)
Dr. Karmach

Practice 1: answer C

SrCl₂(aq) + Na₂CO₃(aq) → SrCO₃(s) + 2 NaCl(aq)
the molecular equation, states from the solubility rules
Sr²⁺(aq) + CO₃²⁻(aq) → SrCO₃(s) (answer C)
atoms: Sr 1 = 1 ✓ · C 1 = 1 ✓ · O 3 = 3 ✓ · charge: left 1(+2) + 1(−2) = 0, right 0 ✓

A is the molecular equation; nothing has been written as ions. B is the complete ionic equation: Na⁺ and Cl⁻ still stand on both sides, uncancelled. D halves both charges: strontium is a group 2 metal, Sr²⁺, and carbonate is CO₃²⁻, so its 1(+1) + 1(−1) = 0 only looks balanced.

An equation can pass the charge check with two wrong charges. Assign each ion's real charge first, then check.
Dr. Karmach

Worked example 3: sodium chloride and potassium nitrate

Step 1 · Write the molecular equation with states

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
partners swapped; the solubility rules mark every compound (aq): no solid

The two solutions are mixed and stay clear: no solid, no gas, no color change. Write the complete ionic equation, then the net ionic equation.

Dr. Karmach

Worked example 3: solution

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
molecular · every compound soluble, every state (aq)

Step 2 · Write each (aq) compound as its ions

Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq) → Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
complete ionic · no solid to keep intact
Dr. Karmach

Worked example 3: solution

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
molecular · every compound soluble, every state (aq)
Step 2 · Write each (aq) compound as its ions
Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq) → Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
complete ionic · no solid to keep intact
Step 3 · Cancel the spectator ions

All four ions appear identical on both sides. Every ion is a spectator.

Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq) → Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
4 − 4 = 0 ions remain: no net ionic equation
Dr. Karmach

Worked example 3: solution

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
molecular · every compound soluble, every state (aq)
Step 2 · Write each (aq) compound as its ions
Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq) → Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
complete ionic · no solid to keep intact
Step 3 · Cancel the spectator ions
Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq) → Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
4 − 4 = 0 ions remain: no net ionic equation
Mixing produced one solution holding the same four ions. When everything cancels, no reaction occurred, which is exactly what the clear beaker showed.
Dr. Karmach

Worked example 3: the route on the strip

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
split: all four compounds · kept whole: none · found: every ion cancels

Every formula took the yes branch, so nothing was left to build a solid, water or a gas. All ions cancel: no reaction. ✓
Dr. Karmach

Practice 2

AgNO₃(aq) + K₂CO₃(aq) → ?
two clear solutions are mixed · a pale yellow solid forms

A few drops of silver nitrate fall into potash solution, K₂CO₃. Which net ionic equation describes the change?

  1. 2 Ag⁺(aq) + CO₃²⁻(aq) → Ag₂CO₃(s)
  2. Ag⁺(aq) + CO₃²⁻(aq) → Ag₂CO₃(s)
  3. K⁺(aq) + NO₃⁻(aq) → KNO₃(s)
  4. 2 Ag⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + CO₃²⁻(aq) → Ag₂CO₃(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
  5. Ag⁺(aq) + CO₃²⁻(aq) → AgCO₃(s)
Dr. Karmach

Practice 2: answer A

2 AgNO₃(aq) + K₂CO₃(aq) → Ag₂CO₃(s) + 2 KNO₃(aq)
molecular · carbonates: insoluble except group 1 and NH₄⁺ · Ag₂CO₃: 2(1+) + 1(2−) = 0 ✓
2 Ag⁺(aq) + CO₃²⁻(aq) → Ag₂CO₃(s) (answer A)
atoms: Ag 2 = 2 ✓ · C 1 = 1 ✓ · O 3 = 3 ✓ · charge: left 2(1+) + 1(2−) = 0, right 0 ✓

B dropped the coefficient: Ag 1 ≠ 2, and charge 1(1+) + 1(2−) = −1 against 0. C precipitated the soluble pair: K⁺ is group 1 and nitrate is always soluble. D is the complete ionic equation, K⁺ and NO₃⁻ uncancelled. E copied a one-to-one ratio into the formula: AgCO₃ sums to 1(1+) + 1(2−) = −1, not neutral.

Two 1+ silvers balance one 2− carbonate. The neutral solid sets the 2 : 1 ratio, and the charge check confirms it.
Dr. Karmach

Worked example 4: acid plus base

Step 1 · Write the molecular equation with states

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
HCl: a strong acid, all ions in water · NaOH: a soluble ionic compound · H₂O(l): a covalent liquid

Mixing hydrochloric acid with sodium hydroxide solution gives salt water: nothing visible happens, yet the beaker warms. Write the complete ionic equation, then the net ionic equation.

Dr. Karmach

Worked example 4: the complete ionic equation

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
molecular · all three (aq) compounds are strong electrolytes

Step 2 · Write each (aq) compound as its ions

All three (aq) compounds separate completely. Water is a covalent molecule: it stays whole.

H⁺(aq) + Cl⁻(aq) + Na⁺(aq) + OH⁻(aq) → Na⁺(aq) + Cl⁻(aq) + H₂O(l)
charge: left 1(1+) + 1(1−) + 1(1+) + 1(1−) = 0 · right 1(1+) + 1(1−) + 0 = 0 ✓
Dr. Karmach

Worked example 4: the complete ionic equation

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
molecular · all three (aq) compounds are strong electrolytes
Step 2 · Write each (aq) compound as its ions
H⁺(aq) + Cl⁻(aq) + Na⁺(aq) + OH⁻(aq) → Na⁺(aq) + Cl⁻(aq) + H₂O(l)
charge: left 1(1+) + 1(1−) + 1(1+) + 1(1−) = 0 · right 1(1+) + 1(1−) + 0 = 0 ✓
Step 3 · Cancel the spectator ions
H⁺(aq) + Cl⁻(aq) + Na⁺(aq) + OH⁻(aq) → Na⁺(aq) + Cl⁻(aq) + H₂O(l)
spectators: Na⁺ and Cl⁻ · the salt of the molecular equation never left the water
Dr. Karmach

Worked example 4: the complete ionic equation

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
molecular · all three (aq) compounds are strong electrolytes
Step 2 · Write each (aq) compound as its ions
H⁺(aq) + Cl⁻(aq) + Na⁺(aq) + OH⁻(aq) → Na⁺(aq) + Cl⁻(aq) + H₂O(l)
charge: left 1(1+) + 1(1−) + 1(1+) + 1(1−) = 0 · right 1(1+) + 1(1−) + 0 = 0 ✓
Step 3 · Cancel the spectator ions
H⁺(aq) + Cl⁻(aq) + Na⁺(aq) + OH⁻(aq) → Na⁺(aq) + Cl⁻(aq) + H₂O(l)
spectators: Na⁺ and Cl⁻ · the salt of the molecular equation never left the water
No solid forms this time. The product that drives the reaction is the covalent molecule H₂O, and it keeps its H and O out of the ion pool.
Dr. Karmach

Worked example 4: the net ionic equation

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
molecular · spectators already cancelled: Na⁺ and Cl⁻

Step 4 · Check atoms and charge

H⁺(aq) + OH⁻(aq) → H₂O(l)
atoms: H 1 + 1 = 2 ✓ · O 1 = 1 ✓ · charge: left 1(1+) + 1(1−) = 0, right 0 ✓
Dr. Karmach

Worked example 4: the net ionic equation

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
molecular · spectators already cancelled: Na⁺ and Cl⁻

Step 4 · Check atoms and charge

H⁺(aq) + OH⁻(aq) → H₂O(l)
atoms: H 1 + 1 = 2 ✓ · O 1 = 1 ✓ · charge: left 1(1+) + 1(1−) = 0, right 0 ✓
Every strong acid neutralizing every soluble hydroxide gives this same net line, so long as the salt formed stays dissolved.
Dr. Karmach

Worked example 4: the net ionic equation

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
molecular · spectators already cancelled: Na⁺ and Cl⁻

Step 4 · Check atoms and charge

H⁺(aq) + OH⁻(aq) → H₂O(l)
atoms: H 1 + 1 = 2 ✓ · O 1 = 1 ✓ · charge: left 1(1+) + 1(1−) = 0, right 0 ✓
Every strong acid neutralizing every soluble hydroxide gives this same net line, so long as the salt formed stays dissolved.
One net ionic equation stands behind thousands of acid-base pairs: H⁺ meets OH⁻ and leaves the ion pool as water.
Dr. Karmach

Worked example 4: a weak acid instead

HCN(aq) + NaOH(aq) → NaCN(aq) + H₂O(l)
molecular · HCN: a weak acid, almost every molecule stays whole in water

The weak-acid case

A weak acid is not written as ions: the water really holds HCN molecules.

Dr. Karmach

Worked example 4: a weak acid instead

HCN(aq) + NaOH(aq) → NaCN(aq) + H₂O(l)
molecular · HCN: a weak acid, almost every molecule stays whole in water

The weak-acid case

A weak acid is not written as ions: the water really holds HCN molecules.

HCN(aq) + OH⁻(aq) → CN⁻(aq) + H₂O(l)
net ionic · Na⁺ is the only spectator · atoms: H 1 + 1 = 2 ✓ · C 1 = 1 ✓ · N 1 = 1 ✓ · O 1 = 1 ✓ · charge: left 0 + 1(1−) = 1−, right 1(1−) + 0 = 1− ✓
Dr. Karmach

Worked example 4: a weak acid instead

HCN(aq) + NaOH(aq) → NaCN(aq) + H₂O(l)
molecular · HCN: a weak acid, almost every molecule stays whole in water

The weak-acid case

A weak acid is not written as ions: the water really holds HCN molecules.

HCN(aq) + OH⁻(aq) → CN⁻(aq) + H₂O(l)
net ionic · Na⁺ is the only spectator · atoms: H 1 + 1 = 2 ✓ · C 1 = 1 ✓ · N 1 = 1 ✓ · O 1 = 1 ✓ · charge: left 0 + 1(1−) = 1−, right 1(1−) + 0 = 1− ✓
The acid appears whole because that is what the solution contains. A net ionic equation may carry a nonzero total charge, as long as both sides match.
Dr. Karmach

Worked example 4: the route on the strip

HCN(aq) + NaOH(aq) → NaCN(aq) + H₂O(l)
split: NaOH, NaCN · kept whole: HCN (weak acid), H₂O(l) · found: HCN(aq) + OH⁻(aq) → CN⁻(aq) + H₂O(l)

With HCl, only water takes the no branch. With HCN, the weak acid takes it too, so the acid enters the net ionic equation whole. ✓
Dr. Karmach

Worked example 5: a metal dissolves in acid

Step 1 · Write the molecular equation with states

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
not every net ionic equation is a precipitation · Mg(s) and H₂(g): not dissolved, kept whole

Magnesium ribbon dropped into hydrochloric acid fizzes and shrinks until it is gone. Write the complete ionic equation, then the net ionic equation.

Dr. Karmach

Worked example 5: solution

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
molecular · only the (aq) compounds separate

Step 2 · Write each (aq) compound as its ions

The solid metal and the gas stay whole; only the two (aq) compounds separate.

Mg(s) + 2 H⁺(aq) + 2 Cl⁻(aq) → Mg²⁺(aq) + 2 Cl⁻(aq) + H₂(g)
charge: left 0 + 2(1+) + 2(1−) = 0 · right 1(2+) + 2(1−) + 0 = 0 ✓
Dr. Karmach

Worked example 5: solution

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
molecular · only the (aq) compounds separate
Step 2 · Write each (aq) compound as its ions
Mg(s) + 2 H⁺(aq) + 2 Cl⁻(aq) → Mg²⁺(aq) + 2 Cl⁻(aq) + H₂(g)
charge: left 0 + 2(1+) + 2(1−) = 0 · right 1(2+) + 2(1−) + 0 = 0 ✓
Step 3 · Cancel the spectator ions Step 4 · Check atoms and charge
Mg(s) + 2 H⁺(aq) → Mg²⁺(aq) + H₂(g)
spectator: Cl⁻ · atoms: Mg 1 = 1 ✓ · H 2 = 2 ✓ · charge: left 0 + 2(1+) = 2+, right 1(2+) + 0 = 2+ ✓
Dr. Karmach

Worked example 5: solution

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
molecular · only the (aq) compounds separate
Step 2 · Write each (aq) compound as its ions
Mg(s) + 2 H⁺(aq) + 2 Cl⁻(aq) → Mg²⁺(aq) + 2 Cl⁻(aq) + H₂(g)
charge: left 0 + 2(1+) + 2(1−) = 0 · right 1(2+) + 2(1−) + 0 = 0 ✓
Step 3 · Cancel the spectator ions Step 4 · Check atoms and charge
Mg(s) + 2 H⁺(aq) → Mg²⁺(aq) + H₂(g)
spectator: Cl⁻ · atoms: Mg 1 = 1 ✓ · H 2 = 2 ✓ · charge: left 0 + 2(1+) = 2+, right 1(2+) + 0 = 2+ ✓
Both sides carry 2+: the check demands equal charge, not zero charge. A net ionic equation can describe more than precipitation.
Dr. Karmach

Worked example 5: the route on the strip

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
split: HCl, MgCl₂ · kept whole: Mg(s), H₂(g) · found: Mg(s) + 2 H⁺(aq) → Mg²⁺(aq) + H₂(g)

The solid metal and the gas took the no branch and stay whole. HCl and MgCl₂ split, and only Cl⁻ cancels. ✓
Dr. Karmach

Practice 3

FeCl₃(aq) + 3 NaOH(aq) → Fe(OH)₃(s) + 3 NaCl(aq)
molecular · Fe(OH)₃ is the rust-orange precipitate

Iron(III) chloride meets sodium hydroxide in water treatment. Which is the correct net ionic equation?

  1. Fe³⁺(aq) + 3 OH⁻(aq) → Fe(OH)₃(s)
  2. Fe³⁺(aq) + OH⁻(aq) → Fe(OH)₃(s)
  3. Fe³⁺(aq) + 3 Cl⁻(aq) + 3 Na⁺(aq) + 3 OH⁻(aq) → Fe(OH)₃(s) + 3 Na⁺(aq) + 3 Cl⁻(aq)
  4. FeCl₃(aq) + 3 NaOH(aq) → Fe(OH)₃(s) + 3 NaCl(aq)
Dr. Karmach

Practice 3: answer A

Fe³⁺(aq) + 3 OH⁻(aq) → Fe(OH)₃(s) (answer A)
atoms: Fe 1 = 1 ✓ · O 3 = 3 ✓ · H 3 = 3 ✓ · charge: left 1(3+) + 3(1−) = 0, right 0 ✓

B dropped the coefficient: 1(3+) + 1(1−) = 2+ against 0, and one OH⁻ cannot supply the three in Fe(OH)₃. C is the complete ionic equation: Na⁺ and Cl⁻ still stand on both sides. D is the molecular equation; nothing has been written as ions.

Three 1− hydroxides cancel one 3+ iron. The neutral solid sets the 3 : 1 ratio before any cancelling starts.
Dr. Karmach

Practice 4

K₂CO₃(aq) + BaCl₂(aq) → BaCO₃(s) + 2 KCl(aq)
molecular · BaCO₃ is the white precipitate

Potassium carbonate and barium chloride solutions are mixed. Which is the correct net ionic equation?

  1. Ba⁺(aq) + CO₃⁻(aq) → BaCO₃(s)
  2. K⁺(aq) + Cl⁻(aq) → KCl(s)
  3. Ba²⁺(aq) + 2 Cl⁻(aq) + 2 K⁺(aq) + CO₃²⁻(aq) → BaCO₃(s) + 2 K⁺(aq) + 2 Cl⁻(aq)
  4. Ba²⁺(aq) + CO₃²⁻(aq) → BaCO₃(s)
Dr. Karmach

Practice 4: answer D

Ba²⁺(aq) + CO₃²⁻(aq) → BaCO₃(s) (answer D)
atoms: Ba 1 = 1 ✓ · C 1 = 1 ✓ · O 3 = 3 ✓ · charge: left 1(2+) + 1(2−) = 0, right 0 ✓

B builds the wrong product: KCl passes the solubility rules, so its ions stay dissolved and KCl(s) never forms. C is the complete ionic equation with K⁺ and Cl⁻ uncancelled. A halves both charges: barium is a group 2 metal, Ba²⁺, and carbonate is CO₃²⁻; its 1(1+) + 1(1−) = 0 only looks balanced.

Two wrong charges can still sum to zero. Assign each ion's real charge first, then run the check.
Dr. Karmach

Check yourself

  1. K₂SO₄ dissolves in water. List the species actually present, with the charge and count of each.
  2. Cu²⁺(aq) + OH⁻(aq) → Cu(OH)₂(s) is offered as a net ionic equation. Run both checks; correct the equation.

Nearly every (aq) compound here was written as fully separated ions; HCN, kept whole, already hints that not every solute earns the split. How completely a dissolved substance actually separates classifies it as a strong, weak, or non-electrolyte, and it decides which formulas may be split on the page.

Dr. Karmach

5 · Electrolytes & Dissociation

Classify a solute as a strong electrolyte, a weak electrolyte, or a nonelectrolyte from its compound type, and write its dissociation equation with the right ions, coefficients, and charge sum.

Dr. Karmach

Inside a sports drink

The label lists sodium, potassium, chloride. In the bottle, each one travels through the water as a separate charged particle. Nerve and muscle signals run on these moving charges.

Dr. Karmach

Conduction needs moving charges

A solution conducts only if charged particles can move through it. What a solute becomes in water sets how strongly its solution conducts: all ions, a few ions, or no ions at all.

Dr. Karmach

Three classes of solute

strong electrolyte: dissolves entirely as ions
soluble ionic compounds (NaOH, KOH included) · the seven strong acids: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃
weak electrolyte: a small fraction ionizes
weak acids and weak bases: HC₂H₃O₂ · NH₃; most molecules stay whole
nonelectrolyte: dissolves as whole molecules
other molecular compounds: sugar · ethanol; no ions, no conduction

An electrolyte releases ions in water, and its solution conducts. Compound type assigns the class. Acids and bases get strength lists of their own.

Dr. Karmach

Dissociation equations

NaCl(s) → Na⁺(aq) + Cl⁻(aq)
1 + 1 = 2 ions per formula unit · charge: (1+) + (1−) = 0
CaCl₂(s) → Ca²⁺(aq) + 2 Cl⁻(aq)
1 + 2 = 3 ions per formula unit · charge: (2+) + 2(1−) = 0

Water pulls an ionic solid apart into its separate ions: dissociation. Each ion keeps its identity and its charge. A subscript counts separate ions, so it becomes a coefficient.

Dr. Karmach

Polyatomic ions stay in one piece

Na₂SO₄(s) → 2 Na⁺(aq) + SO₄²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0

Dissociation separates cations from anions. It never breaks the bonds inside a polyatomic ion: sulfate enters the water whole, carrying its 2− charge.

Dr. Karmach

Weak electrolytes: partial ionization

HC₂H₃O₂(aq) ⇌ H⁺(aq) + C₂H₃O₂⁻(aq)
most molecules stay whole · each ionization: (1+) + (1−) = 0
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a weak base: only a few molecules react · charge: (1+) + (1−) = 0

A molecular acid or base ionizes: reaction with water makes new ions. A weak one barely reacts: a few molecules ionize, the rest stay whole. The double arrow marks an incomplete reaction.

Dr. Karmach

The method

  1. Classify the solute. Soluble ionic and strong acids: strong. Other acids and bases: weak. Other molecular: nonelectrolyte.
  2. Write what water makes. Separated ions, a few ions, or whole molecules.
  3. Check the charge sum. The ions must total zero.
Dr. Karmach

Worked example 1: magnesium chloride

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation

Road crews spread MgCl₂ as a de-icer, and it dissolves freely. Classify it and write the dissociation equation.

Dr. Karmach

Worked example 1: solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation

Step 1 · Classify the solute

A metal with a nonmetal: ionic. A soluble ionic compound is a strong electrolyte.

Dr. Karmach

Worked example 1: solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit

The subscript counts two separate chloride ions. Each one leaves the lattice on its own.

Dr. Karmach

Worked example 1: solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit
Step 3 · Check the charge sum
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
3 ions · charge: (2+) + 2(1−) = 0 ✓
Dr. Karmach

Worked example 1: solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit
Step 3 · Check the charge sum
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
3 ions · charge: (2+) + 2(1−) = 0 ✓
The solid is neutral, so the ions it releases must cancel: one 2+ against two 1−. A nonzero sum marks a wrong formula or a wrong coefficient. ✓
Dr. Karmach

Worked example 1: the route on the chart

MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
MgCl₂: ionic, soluble · found: strong electrolyte, 3 ions per formula unit

Two yes answers: ionic, then soluble. The acid questions never come up for an ionic solute. ✓
Dr. Karmach

Worked example 2: Na₂CO₃, NH₃, C₂H₅OH

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol · wanted: each class + what each solution contains

All three dissolve freely in water. Classify each and write what its solution contains.

Dr. Karmach

Worked example 2: classifying

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol

Step 1 · Classify the solute

solute type class
Na₂CO₃ soluble ionic compound strong electrolyte
NH₃ molecular base, not an ionic hydroxide weak electrolyte
C₂H₅OH molecular, neither acid nor base nonelectrolyte
Dr. Karmach

Worked example 2: classifying

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol

Step 1 · Classify the solute

solute type class
Na₂CO₃ soluble ionic compound strong electrolyte
NH₃ molecular base, not an ionic hydroxide weak electrolyte
C₂H₅OH molecular, neither acid nor base nonelectrolyte
All three bottles look identical. The compound type, not the appearance, separates them.
Dr. Karmach

Worked example 2: what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
Dr. Karmach

Worked example 2: what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
Dr. Karmach

Worked example 2: what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
C₂H₅OH(aq): dissolves as whole molecules
0 ions · the OH is covalently bonded, not OH⁻
Dr. Karmach

Worked example 2: what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
C₂H₅OH(aq): dissolves as whole molecules
0 ions · the OH is covalently bonded, not OH⁻
Three clear solutions, three bulb readings: bright, dim, dark. ✓
Dr. Karmach

Worked example 2: the route on the chart

Na₂CO₃ · NH₃ · C₂H₅OH
Na₂CO₃: ionic, soluble · NH₃: not ionic, not on the acid list, a base · C₂H₅OH: every answer no

Three solutes leave by three exits. Only the ionic one needed the solubility rules. ✓
Dr. Karmach

Your turn: magnesium nitrate

Mg(NO₃)₂(s) dissolved in water
given: a soluble ionic compound · nitrate: NO₃⁻
step work result
1 · classify the solute soluble ionic compound electrolyte
2 · write what water makes Mg(NO₃)₂(s) → Mg²⁺(aq) + ions per formula unit:
3 · check the charge sum (2+) + 2(1−) =

Complete the classification and the equation.

Dr. Karmach

Your turn: magnesium nitrate

Mg(NO₃)₂(s) dissolved in water
given: a soluble ionic compound · nitrate: NO₃⁻
step work result
1 · classify the solute soluble ionic compound electrolyte
2 · write what water makes Mg(NO₃)₂(s) → Mg²⁺(aq) + ions per formula unit:
3 · check the charge sum (2+) + 2(1−) =

Complete the classification and the equation.

Mg(NO₃)₂(s) → Mg²⁺(aq) + 2 NO₃⁻(aq)
strong electrolyte · 1 + 2 = 3 ions · charge: (2+) + 2(1−) = 0 · each nitrate leaves whole
Dr. Karmach

Drill: three dissociation equations

K₂S · (NH₄)₂SO₄ · Al(NO₃)₃
all three: soluble ionic → strong electrolytes · wanted: each equation, ion count, charge sum
solid dissociation ions charge sum
K₂S(s) 2 K⁺(aq) + S²⁻(aq) 2 + 1 = 2(1+) + (2−) =
(NH₄)₂SO₄(s) 2 (aq) + SO₄²⁻(aq) 2 + 1 = 3 2(1+) + (2−) = 0
Al(NO₃)₃(s) Al³⁺(aq) + 1 + 3 = (3+) + 3(1−) = 0

Complete the table.

Dr. Karmach

Drill: three dissociation equations

K₂S · (NH₄)₂SO₄ · Al(NO₃)₃
all three: soluble ionic → strong electrolytes · wanted: each equation, ion count, charge sum
solid dissociation ions charge sum
K₂S(s) 2 K⁺(aq) + S²⁻(aq) 2 + 1 = 2(1+) + (2−) =
(NH₄)₂SO₄(s) 2 (aq) + SO₄²⁻(aq) 2 + 1 = 3 2(1+) + (2−) = 0
Al(NO₃)₃(s) Al³⁺(aq) + 1 + 3 = (3+) + 3(1−) = 0

Complete the table.

K₂S → 2 K⁺ + S²⁻ (3 ions) · (NH₄)₂SO₄ → 2 NH₄⁺ + SO₄²⁻ (3 ions) · Al(NO₃)₃ → Al³⁺ + 3 NO₃⁻ (4 ions)
every charge sum is 0 · both polyatomic ions travel whole: NH₄⁺ and SO₄²⁻
Dr. Karmach

Where this goes wrong

Reading a subscript as a bonded pair. CaCl₂ never releases a Cl₂²⁻ unit. The subscript counts separate ions: Ca²⁺ + 2 Cl⁻ makes 1 + 2 = 3 ions, not 1 + 1 = 2.
Breaking a polyatomic ion into atoms. Na₂CO₃ gives 2 Na⁺ + CO₃²⁻ = 3 ions, never 2 + 1 + 3 = 6 pieces. Dissociation separates ions; it does not break the bonds inside one.
Calling sugar a weak electrolyte. Weak means a few ions form. Sugar forms none: its solution conducts no better than pure water. Nonelectrolyte.
Reading a molecular OH as hydroxide. Ethanol's OH is covalently bonded and stays put. Only ionic hydroxides such as NaOH release OH⁻.
Dr. Karmach

Practice 1

K₃PO₄ dissolved in water
given: a soluble ionic compound · phosphate: PO₄³⁻

Fertilizer-grade potassium phosphate dissolves freely in water. Which statement classifies it and describes what its solution contains?

  1. Weak electrolyte: a salt built around a polyatomic ion dissociates only partially
  2. Strong electrolyte: it dissociates completely into 3 K⁺ and PO₄³⁻, four ions per formula unit
  3. Strong electrolyte: it dissociates completely into K₃⁺ and PO₄³⁻, two ions per formula unit
  4. Nonelectrolyte: it dissolves as intact, neutral K₃PO₄ molecules
Dr. Karmach

Practice 1: answer B

K₃PO₄(s) → 3 K⁺(aq) + PO₄³⁻(aq) (answer B)
3 + 1 = 4 ions · charge: 3(1+) + (3−) = 0

A: solubility decides, not the anion; a soluble salt dissociates completely, polyatomic ion or not. C: the subscript counts three separate K⁺ ions; no K₃⁺ unit exists, and 1 + 1 = 2 undercounts the ions. D: an ionic compound has no molecules; only separated ions enter the water.

Four ions from one formula unit, and the charges cancel: 3(1+) + (3−) = 0. ✓
Dr. Karmach

Worked example 3: ion concentrations

0.100 M AlBr₃ dissolved in water
M, molarity = mol of solute per liter of solution · wanted: the molarity of Br⁻

Aluminum bromide dissolves freely. Every formula unit that dissolves releases its ions into the same liter. Find the concentration of Br⁻ in the solution.

Dr. Karmach

Worked example 3: solution

0.100 M AlBr₃ → ? M Br⁻
M = mol per liter of solution

Step 1 · Classify the solute

A metal with a nonmetal: soluble ionic, a strong electrolyte. Every formula unit dissociates.

Dr. Karmach

Worked example 3: solution

0.100 M AlBr₃ → ? M Br⁻
M = mol per liter of solution
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
AlBr₃(s) → Al³⁺(aq) + 3 Br⁻(aq)
1 + 3 = 4 ions · charge: (3+) + 3(1−) = 0 ✓
Dr. Karmach

Worked example 3: solution

0.100 M AlBr₃ → ? M Br⁻
M = mol per liter of solution
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
AlBr₃(s) → Al³⁺(aq) + 3 Br⁻(aq)
1 + 3 = 4 ions · charge: (3+) + 3(1−) = 0 ✓
Ion molarity · multiply by the coefficient

Each liter holds 0.100 mol of dissolved AlBr₃, and each mole releases 3 mol of Br⁻.

0.100 mol AlBr₃ × 3 mol Br⁻1 mol AlBr₃ = 0.300 mol Br⁻ per liter = 0.300 M
Dr. Karmach

Worked example 3: solution

0.100 M AlBr₃ → ? M Br⁻
M = mol per liter of solution
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
AlBr₃(s) → Al³⁺(aq) + 3 Br⁻(aq)
1 + 3 = 4 ions · charge: (3+) + 3(1−) = 0 ✓
Ion molarity · multiply by the coefficient

Each liter holds 0.100 mol of dissolved AlBr₃, and each mole releases 3 mol of Br⁻.

0.100 mol AlBr₃ × 3 mol Br⁻1 mol AlBr₃ = 0.300 mol Br⁻ per liter = 0.300 M
The subscript became a concentration ratio: 0.300 M Br⁻ against 0.100 M Al³⁺.
Dr. Karmach

Worked example 3: the route on the chart

AlBr₃(s) → Al³⁺(aq) + 3 Br⁻(aq)
AlBr₃: ionic, soluble · found: strong electrolyte · 0.100 M AlBr₃ → 0.300 M Br⁻

The strong exit means every formula unit dissociates. Only then does the coefficient 3 turn 0.100 M AlBr₃ into 0.300 M Br⁻. ✓
Dr. Karmach

Practice 2

Fe₂(SO₄)₃ dissolved in water
given: 0.60 M SO₄²⁻ required · wanted: the molarity of Fe₂(SO₄)₃

A water plant's dosing tank must reach 0.60 M sulfate ion, supplied by dissolving iron(III) sulfate. What molarity of Fe₂(SO₄)₃ does the tank need?

  1. 0.30
  2. 1.8
  3. 0.60
  4. 0.20
Dr. Karmach

Practice 2: answer D

Fe₂(SO₄)₃(s) → 2 Fe³⁺(aq) + 3 SO₄²⁻(aq)
2 + 3 = 5 ions · charge: 2(3+) + 3(2−) = 0 ✓
0.60 mol SO₄²⁻ × 1 mol Fe₂(SO₄)₃3 mol SO₄²⁻ = 0.20 mol Fe₂(SO₄)₃ per liter = 0.20 M (answer D)

C skipped the ratio: 0.60 × 1 = 0.60 M assumes one sulfate per formula unit. B flipped the ratio: 0.60 × 3 = 1.8 M, a tank at 1.8 × 3 = 5.4 M sulfate. A used iron's subscript: 0.60 ÷ 2 = 0.30 M.

Each formula unit releases three sulfates, so the salt runs at one third of the target: 3 × 0.20 = 0.60 M sulfate ✓.
Dr. Karmach

Worked example 4: two acids

HNO₃ and HC₂H₃O₂, each dissolved in water
given: two molecular acids · wanted: each class + what each solution contains

Nitric acid and acetic acid both dissolve freely, in any proportion. A common first attempt: both are acids, so both ionize completely. Test it.

Dr. Karmach

Worked example 4: solution

HNO₃ and HC₂H₃O₂, each dissolved in water

A common first attempt

both acids → all ions?
the strong-acid list: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃; HC₂H₃O₂ is not on it ✗

Dissolving freely is not ionizing. Mixing spreads molecules through the water; only reaction with water makes ions.

Dr. Karmach

Worked example 4: solution

HNO₃ and HC₂H₃O₂, each dissolved in water
A common first attempt
both acids → all ions?
the strong-acid list: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃; HC₂H₃O₂ is not on it ✗
Step 1 · Classify the solute

HNO₃ is on the list: a strong electrolyte. HC₂H₃O₂ is not, and an acid off the list is weak.

Dr. Karmach

Worked example 4: solution

HNO₃ and HC₂H₃O₂, each dissolved in water
A common first attempt
both acids → all ions?
the strong-acid list: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃; HC₂H₃O₂ is not on it ✗
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
HNO₃(aq) → H⁺(aq) + NO₃⁻(aq)
every molecule ionizes · 1 + 1 = 2 ions · charge: (1+) + (1−) = 0
HC₂H₃O₂(aq) ⇌ H⁺(aq) + C₂H₃O₂⁻(aq)
a few molecules ionize, the rest stay whole · charge: (1+) + (1−) = 0
Dr. Karmach

Worked example 4: solution

HNO₃ and HC₂H₃O₂, each dissolved in water
A common first attempt
both acids → all ions?
the strong-acid list: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃; HC₂H₃O₂ is not on it ✗
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
HNO₃(aq) → H⁺(aq) + NO₃⁻(aq)
every molecule ionizes · 1 + 1 = 2 ions · charge: (1+) + (1−) = 0
HC₂H₃O₂(aq) ⇌ H⁺(aq) + C₂H₃O₂⁻(aq)
a few molecules ionize, the rest stay whole · charge: (1+) + (1−) = 0
Both conduct, not equally: HNO₃ all ions, HC₂H₃O₂ mostly whole molecules: a dim bulb. ✓
Dr. Karmach

Worked example 4: the route on the chart

HNO₃ and HC₂H₃O₂
HNO₃: not ionic, on the strong-acid list · HC₂H₃O₂: not ionic, off the list, another acid

Both acids skip the solubility question. The strong-acid list alone splits them: one exit bright, one dim. ✓
Dr. Karmach

Take-home: dissolving is not ionizing

HNO₃: on the strong-acid list
dissolves freely and ionizes completely: all ions in solution
HC₂H₃O₂: not on the list
dissolves just as freely, barely ionizes: mostly whole molecules

Solubility measures how much dissolves. Electrolyte strength measures what the dissolved substance becomes. An acid is a strong electrolyte only if it is on the memorized list; every other acid is weak.

Dr. Karmach

Practice 3

HClO₄ · HF · C₁₂H₂₂O₁₁ · NaF
perchloric acid · hydrofluoric acid · sucrose · sodium fluoride · equal concentrations

Each solution is tested with a light-bulb conductivity tester. Which solution lights the bulb only dimly?

  1. HF
  2. HClO₄
  3. C₁₂H₂₂O₁₁
  4. NaF
Dr. Karmach

Practice 3: answer A

HF(aq) ⇌ H⁺(aq) + F⁻(aq) (answer A)
an acid off the strong list: weak electrolyte · a few molecules ionize · charge: (1+) + (1−) = 0

B is on the strong-acid list (HCl, HBr, HI, HNO₃, H₂SO₄, HClO₄, HClO₃): every molecule ionizes, and the bulb glows bright. C is molecular and neither acid nor base: sucrose dissolves as whole molecules, and the bulb stays dark. D shares fluorine with HF but is a soluble ionic compound: NaF → Na⁺ + F⁻ dissociates completely, a bright bulb.

Four solutes, three classes: bright (HClO₄, NaF), dim (HF), dark (sucrose). The compound type decides, not the elements it contains.
Dr. Karmach

Check yourself

  1. K₂S dissolves freely in water. Name its class, write the dissociation equation, and check the ion tally and the charge sum.
  2. A solution conducts, but only faintly. Which class is the solute, and what does the solution mostly contain?

Every (aq) compound in a reaction equation is shorthand for these separated ions. Which new pairings leave the water, and which ions only watch, is exactly what the solubility rules and the net ionic equation track. The acids and bases among these solutes get their own strong and weak lists, and those lists decide which of them count as fully separated.

Dr. Karmach

6 · Acids and Bases, Strong vs Weak

Classify any acid or base as strong or weak using the memorize-lists, write its ionization with the correct arrow (→ for full, ⇌ for partial), and predict the products of neutralization and gas-evolution reactions.

Dr. Karmach

Strong is not the same as a lot

Stomach acid is hydrochloric acid, HCl, a strong acid, yet dilute. Strong and weak describe how completely an acid ionizes, not how much of it is dissolved.

Dr. Karmach

What makes something an acid or a base

Dissolved in water, an acid produces H⁺, carried as the hydronium ion H₃O⁺. A base produces OH⁻.

acid → H⁺ (H₃O⁺) in water · base → OH⁻ in water
Arrhenius definitions · Brønsted–Lowry widens them: an acid donates a proton (H⁺), a base accepts one

Every acid here has an H to release; every hydroxide carries its OH⁻.

Dr. Karmach

Strong vs weak = the degree of ionization

Strong means essentially every molecule ionizes; weak means a small fraction. The ⇌ arrow marks the reverse reaction: ions rejoin as fast as molecules split, so the mixture settles mostly intact.

HCl → H⁺ + Cl⁻ (≈100%, one → arrow) · CH₃COOH ⇌ H⁺ + CH₃COO⁻ (partial, ⇌)
strong = fully ionized = a strong electrolyte · weak = barely ionized = a weak electrolyte
Dr. Karmach

What a 1 M acid bottle contains

a bottle labeled 1 M HCl actually has no HCl in it, but 1 M H⁺(aq) and 1 M Cl⁻(aq)
strong acid: every molecule ionized · nothing left to match the label
a bottle labeled 1 M HA, where HA is a weak acid, actually has mostly HA in it and only a small amount of H⁺(aq) and A⁻(aq)
weak acid: the molecules survive · few ions

The label names what was dissolved. The strong or weak classification tells what the water holds now.

Dr. Karmach

The seven strong acids: memorize them

Only seven common acids are strong; everything not on the list is weak. The list is measured, not deduced: these seven ionize essentially completely in water.

HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃
3 hydrohalic (HCl, HBr, HI) + 4 oxoacids (HNO₃, H₂SO₄, HClO₄, HClO₃) = 3 + 4 = 7
not on it: CH₃COOH · HF · H₂CO₃ · H₃PO₄ → all weak, partial ionization (⇌)
the structural reason for the split waits for equilibrium
Dr. Karmach

Strong bases, and neutralization

The strong bases are the metal hydroxides that ionize completely: every group 1 hydroxide, plus the heavy group 2 hydroxides.

group 1: LiOH NaOH KOH RbOH CsOH · group 2 (heavy): Ca(OH)₂ Sr(OH)₂ Ba(OH)₂
5 + 3 = 8 strong bases · Ca(OH)₂ → Ca²⁺ + 2 OH⁻ releases 2 × 1 = 2 hydroxide ions · Ca(OH)₂ and Sr(OH)₂ barely dissolve (the chart says insoluble), but all that dissolves ionizes fully
NH₃ + H₂O ⇌ NH₄⁺ + OH⁻ · acid + base → salt + water
ammonia and amines make OH⁻ only partially: weak bases · an acid and a base neutralize to a salt plus water

Ammonia and the amines are weak bases. An acid and a base neutralize each other.

Dr. Karmach

The method

  1. Acid or base? An H to release: acid. Hydroxide or NH₃/amine: base.
  2. On a memorize list? Listed: strong. Not listed: weak.
  3. Pick the arrow. Strong ionizes fully: →. Weak, partially: ⇌.
  4. Ignore concentration. Strength is the fraction ionized.
Dr. Karmach

Worked example 1: classify three species

HNO₃ · HF · Ca(OH)₂
for each: strong or weak? which electrolyte? which arrow: → or ⇌?

Nitric acid, hydrofluoric acid, and calcium hydroxide. Check each against the memorize-lists, then write how it behaves in water.

Dr. Karmach

Worked example 1: solution

HNO₃ · on the strong-acid list

HNO₃ is one of the seven strong acids, so it ionizes completely: a strong electrolyte.

HNO₃ → H⁺ + NO₃⁻
full ionization, single → arrow · 1 + 1 = 2 ions per formula unit
Dr. Karmach

Worked example 1: solution

HNO₃ · on the strong-acid list

HNO₃ → H⁺ + NO₃⁻
full ionization, single → arrow · 1 + 1 = 2 ions per formula unit
HF · not on the list → weak

HF is not one of the seven, so it is a weak acid: a weak electrolyte, partial ionization.

HF ⇌ H⁺ + F⁻
mostly intact HF molecules · the ⇌ arrow marks partial ionization
Dr. Karmach

Worked example 1: solution

HNO₃ · on the strong-acid list

HNO₃ → H⁺ + NO₃⁻
full ionization, single → arrow · 1 + 1 = 2 ions per formula unit
HF · not on the list → weak
HF ⇌ H⁺ + F⁻
mostly intact HF molecules · the ⇌ arrow marks partial ionization
Ca(OH)₂ · a heavy group 2 hydroxide → strong base
Ca(OH)₂ → Ca²⁺ + 2 OH⁻
strong base, strong electrolyte · 1 + 2 = 3 ions, of which 2 × 1 = 2 are OH⁻
Dr. Karmach

Worked example 1: solution

HNO₃ · on the strong-acid list

HNO₃ → H⁺ + NO₃⁻
full ionization, single → arrow · 1 + 1 = 2 ions per formula unit
HF · not on the list → weak
HF ⇌ H⁺ + F⁻
mostly intact HF molecules · the ⇌ arrow marks partial ionization
Ca(OH)₂ · a heavy group 2 hydroxide → strong base
Ca(OH)₂ → Ca²⁺ + 2 OH⁻
strong base, strong electrolyte · 1 + 2 = 3 ions, of which 2 × 1 = 2 are OH⁻
On the lists, HNO₃ and Ca(OH)₂ ionize fully (→); HF is off the list, mostly intact (⇌).
Dr. Karmach

Worked example 1: the route on the chart

HNO₃ → H⁺ + NO₃⁻ · HF ⇌ H⁺ + F⁻ · Ca(OH)₂ → Ca²⁺ + 2 OH⁻
HNO₃: acid, one of the seven · HF: acid, not one of the seven · Ca(OH)₂: base, a strong base

Three formulas leave by three exits. Only the two lists decided strong or weak. ✓
Dr. Karmach

Where this goes wrong

"HF is strong because F is so electronegative." Electronegativity does not decide it: HF is simply not on the list of seven, so it is weak (⇌).
"Concentrated means strong." Concentration is amount dissolved; strength is the fraction ionized. 10 M acetic acid is still weak; 0.01 M HCl is still strong.
Sulfuric ↔ acetic mix-up. H₂SO₄ is on the list (strong, →); acetic acid CH₃COOH is not (weak, ⇌). Being an acid does not make it strong.
"NH₃ can't be a base: it has no OH." It makes OH⁻ by pulling H⁺ off water: NH₃ + H₂O ⇌ NH₄⁺ + OH⁻: a weak base.
Dr. Karmach

Practice 1: spot the exception

Three of these ionize essentially 100% in water. Which one is not a strong acid?

  1. HClO₄
  2. HCl
  3. HClO
  4. HNO₃
Dr. Karmach

Practice 1: answer C

HClO ⇌ H⁺ + ClO⁻: a weak acid (answer C)
HClO (hypochlorous) is not among the seven; HClO₄, HCl, HNO₃ all are

Watch the chlorine oxoacids: HClO₄ (perchloric) and HClO₃ (chloric) are on the strong list, but HClO (hypochlorous) is weak: it ionizes only partially (⇌). HCl and HNO₃ are strong (→).

Two fewer oxygens separate HClO₃, strong, from HClO, weak. Classify from the list, not from the look of the formula.
Dr. Karmach

Practice 2

1.0 M HNO₂ · 1.0 M NaNO₂
nitrous acid: not on the list of seven · sodium nitrite: a soluble salt

Two bottles, same concentration. Which solution has the higher ion concentration?

  1. 1.0 M HNO₂: it is an acid, and acids ionize completely
  2. 1.0 M NaNO₂: a soluble salt dissociates completely, so it puts far more ions in the water
  3. They are equal: both dissolve completely, so both separate completely
  4. Neither: both dissolve as whole molecules
Dr. Karmach

Practice 2: answer B

NaNO₂(s) → Na⁺(aq) + NO₂⁻(aq) · HNO₂(aq) ⇌ H⁺(aq) + NO₂⁻(aq) (answer B)
the salt delivers 1.0 + 1.0 = 2.0 M of ions · the weak acid delivers far less: most HNO₂ stays whole

A assumes every acid ionizes fully; only the seven on the list do, and HNO₂ is not one. C reads dissolves completely as ionizes completely; both dissolve fully, but only the salt separates fully. D misclassifies NaNO₂: a metal with a polyatomic anion is ionic, and a soluble ionic compound always dissociates.

Same NO₂⁻ anion in both bottles. The partner decides the ion count: Na⁺ lets go completely; the acid's H does not.
Dr. Karmach

Practice 3

1 M HCl · 1 M HF
same concentration · acidity tracks [H₃O⁺]

Which solution is more acidic?

  1. 1 M HCl: strong, fully ionized, so its [H₃O⁺] is the full 1 M; HF ionizes only slightly
  2. 1 M HF: fluorine is more electronegative, so HF releases its H⁺ more readily
  3. They are equally acidic: both hold 1 M of dissolved acid
  4. 1 M HF: weak means the H⁺ is weakly held, so it comes off more easily
Dr. Karmach

Practice 3: answer A

HCl → H⁺ + Cl⁻ (all of it) · HF ⇌ H⁺ + F⁻ (a small fraction) (answer A)
1 M HCl: 1 × 1 = 1 M H₃O⁺ · 1 M HF: far less

B ranks by electronegativity; the list of seven is measured behavior, and HF is not on it. C confuses concentration with strength: both bottles hold 1 M of acid, but they deliver very different amounts of H₃O⁺. D inverts the vocabulary: weak describes the fraction ionized, not a loose grip on H⁺; the weak acid is the one that keeps its H.

Strong and weak are measured ionization, never electronegativity and never concentration.
Dr. Karmach

Worked example 2: predict and balance a neutralization

H₃PO₄(aq) + Ca(OH)₂(aq) → ?
acid + base → salt + water · wanted: the products and the coefficients

Phosphoric acid meets calcium hydroxide. One HCl releases one H⁺: monoprotic. H₂SO₄ releases two: diprotic. H₃PO₄ releases three: triprotic. Predict both products, then balance.

Dr. Karmach

Worked example 2: the products

H₃PO₄(aq) + Ca(OH)₂(aq) → ?
wanted: the products and the coefficients

Predict the products

The salt pairs Ca²⁺ with PO₄³⁻; charge balance builds Ca₃(PO₄)₂. The other product of every neutralization is water.

Dr. Karmach

Worked example 2: the products

H₃PO₄(aq) + Ca(OH)₂(aq) → ?
wanted: the products and the coefficients

Predict the products

The salt pairs Ca²⁺ with PO₄³⁻; charge balance builds Ca₃(PO₄)₂. The other product of every neutralization is water.

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
Ca₃(PO₄)₂: 3(2+) + 2(3−) = 0 ✓
Dr. Karmach

Worked example 2: the products

H₃PO₄(aq) + Ca(OH)₂(aq) → ?
wanted: the products and the coefficients

Predict the products

The salt pairs Ca²⁺ with PO₄³⁻; charge balance builds Ca₃(PO₄)₂. The other product of every neutralization is water.

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
Ca₃(PO₄)₂: 3(2+) + 2(3−) = 0 ✓
The salt's formula comes from the ion charges, never from the coefficients: the products must be neutral before any balancing starts.
Dr. Karmach

Worked example 2: the coefficients

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
products predicted · wanted: the coefficients

Match H⁺ to OH⁻

Balancing a neutralization needs equal moles of H⁺ and OH⁻: one water forms per pair. Three H⁺ against two OH⁻ meet at six: write 2 H₃PO₄ and 3 Ca(OH)₂.

2 H₃PO₄ + 3 Ca(OH)₂ → Ca₃(PO₄)₂ + 6 H₂O
H⁺: 2 × 3 = 6 · OH⁻: 3 × 2 = 6 · 6 pairs → 6 H₂O
Dr. Karmach

Worked example 2: the coefficients

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
products predicted · wanted: the coefficients
Match H⁺ to OH⁻
2 H₃PO₄ + 3 Ca(OH)₂ → Ca₃(PO₄)₂ + 6 H₂O
H⁺: 2 × 3 = 6 · OH⁻: 3 × 2 = 6 · 6 pairs → 6 H₂O
Recheck every count
2 H₃PO₄(aq) + 3 Ca(OH)₂(aq) → Ca₃(PO₄)₂(s) + 6 H₂O(l)
Ca: 3 = 3 ✓ · P: 2 = 2 ✓ · H: 6 + 6 = 12 = 12 ✓ · O: 8 + 6 = 14 = 14 ✓
Dr. Karmach

Worked example 2: the coefficients

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
products predicted · wanted: the coefficients
Match H⁺ to OH⁻
2 H₃PO₄ + 3 Ca(OH)₂ → Ca₃(PO₄)₂ + 6 H₂O
H⁺: 2 × 3 = 6 · OH⁻: 3 × 2 = 6 · 6 pairs → 6 H₂O
Recheck every count
2 H₃PO₄(aq) + 3 Ca(OH)₂(aq) → Ca₃(PO₄)₂(s) + 6 H₂O(l)
Ca: 3 = 3 ✓ · P: 2 = 2 ✓ · H: 6 + 6 = 12 = 12 ✓ · O: 8 + 6 = 14 = 14 ✓
The coefficients 2 and 3 came from matching six H⁺ to six OH⁻, and one water forms per pair: 6 H₂O.
Dr. Karmach

Worked example 2: the route on the chart

2 H₃PO₄(aq) + 3 Ca(OH)₂(aq) → Ca₃(PO₄)₂(s) + 6 H₂O(l)
partner: a hydroxide · exchange: salt + water · nothing breaks up

A hydroxide partner stops after the exchange: a salt and water, no gas. ✓
Dr. Karmach

Worked example 3: acid plus a carbonate

Na₂CO₃(aq) + 2 HCl(aq) → ?
wanted: the products, found in two steps

Washing soda meets hydrochloric acid, and the mixture fizzes. The gas is the product to explain. Work the exchange first, then watch what the exchange product does.

Dr. Karmach

Worked example 3: the exchange

Na₂CO₃(aq) + 2 HCl(aq) → ?
the mixture fizzes: a gas leaves

First reaction · exchange partners

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
Dr. Karmach

Worked example 3: the exchange

Na₂CO₃(aq) + 2 HCl(aq) → ?
the mixture fizzes: a gas leaves

First reaction · exchange partners

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
The exchange is ordinary. The product H₂CO₃, carbonic acid, is not: it cannot survive in water.
Dr. Karmach

Worked example 3: the exchange

Na₂CO₃(aq) + 2 HCl(aq) → ?
the mixture fizzes: a gas leaves

First reaction · exchange partners

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
The exchange is ordinary. The product H₂CO₃, carbonic acid, is not: it cannot survive in water.
On paper the swap looks routine. The fizz says otherwise: one of these products refuses to stay in the water.
Dr. Karmach

Worked example 3: the gas appears

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
the exchange product H₂CO₃ cannot survive in water

Second reaction · the unstable product breaks up

H₂CO₃(aq) → H₂O(l) + CO₂(g)
H: 2 = 2 · C: 1 = 1 · O: 3 = 1 + 2 = 3 ✓ · the fizz is CO₂ leaving
Dr. Karmach

Worked example 3: the gas appears

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
the exchange product H₂CO₃ cannot survive in water
Second reaction · the unstable product breaks up
H₂CO₃(aq) → H₂O(l) + CO₂(g)
H: 2 = 2 · C: 1 = 1 · O: 3 = 1 + 2 = 3 ✓ · the fizz is CO₂ leaving
Overall
Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂O(l) + CO₂(g)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
Dr. Karmach

Worked example 3: the gas appears

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
the exchange product H₂CO₃ cannot survive in water
Second reaction · the unstable product breaks up
H₂CO₃(aq) → H₂O(l) + CO₂(g)
H: 2 = 2 · C: 1 = 1 · O: 3 = 1 + 2 = 3 ✓ · the fizz is CO₂ leaving
Overall
Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂O(l) + CO₂(g)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
Acid plus a carbonate or bicarbonate always ends here: CO₂, water, and a salt. The two-step explains the fizz that one overall line hides.
Dr. Karmach

Worked example 3: the route on the chart

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂O(l) + CO₂(g)
partner: a carbonate · exchange: NaCl + H₂CO₃ · H₂CO₃ breaks up

A carbonate partner runs the full lane: the exchange, then the breakup into water and CO₂. ✓
Dr. Karmach

Three products that never survive

H₂CO₃ → H₂O(l) + CO₂(g) · H₂SO₃ → H₂O(l) + SO₂(g) · NH₄OH → H₂O(l) + NH₃(g)
memorize all three · each breaks into water plus a gas the moment it forms

Three exchange products are unstable. When one appears among the products, replace it with its water and gas. Acid plus a carbonate or bicarbonate always gives CO₂, water, and a salt.

Dr. Karmach

Your turn: acid plus a sulfite

K₂SO₃(aq) + 2 HCl(aq) → ?
exchange first · then check the unstable-products list
step your work
exchange partners 2 KCl +
unstable product breaks up H₂SO₃ → H₂O(l) +
overall equation K₂SO₃(aq) + 2 HCl(aq) → 2 KCl(aq) + +

Complete all three lines.

Dr. Karmach

Your turn: acid plus a sulfite

K₂SO₃(aq) + 2 HCl(aq) → ?
exchange first · then check the unstable-products list
step your work
exchange partners 2 KCl +
unstable product breaks up H₂SO₃ → H₂O(l) +
overall equation K₂SO₃(aq) + 2 HCl(aq) → 2 KCl(aq) + +

Complete all three lines.

K₂SO₃(aq) + 2 HCl(aq) → 2 KCl(aq) + H₂O(l) + SO₂(g)
K: 2 = 2 · S: 1 = 1 · O: 3 = 1 + 2 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
An acid meeting a sulfite releases SO₂, the sharp smell of a struck match.
Dr. Karmach

Practice 4

NaHCO₃(aq) + CH₃COOH(aq) → ?
baking soda + vinegar's acetic acid

Baking soda is stirred into vinegar. Which products form?

  1. NaCH₃COO(aq) + H₂CO₃(aq)
  2. NaCH₃COO(aq) + H₂(g)
  3. No reaction: acetic acid is weak, so its molecules stay whole
  4. NaCH₃COO(aq) + H₂O(l) + CO₂(g)
Dr. Karmach

Practice 4: answer D

NaHCO₃(aq) + CH₃COOH(aq) → NaCH₃COO(aq) + H₂CO₃(aq)
first reaction: exchange partners · H₂CO₃ is on the never-survive list
NaHCO₃(aq) + CH₃COOH(aq) → NaCH₃COO(aq) + H₂O(l) + CO₂(g) (answer D)
Na: 1 = 1 · C: 1 + 2 = 3 = 2 + 1 · H: 1 + 4 = 5 = 3 + 2 · O: 3 + 2 = 5 = 2 + 1 + 2 ✓

A stopped at the exchange: H₂CO₃ breaks into H₂O and CO₂ the moment it forms. B expects H₂, the gas an acid releases from an active metal; a bicarbonate trades partners instead. C reads weak as unreactive: weak describes the fraction ionized, and acid plus a carbonate or bicarbonate always gives CO₂, water, and a salt.

The fizz in the cup is the CO₂ from the H₂CO₃ breakup, even with a weak acid.
Dr. Karmach

Check yourself

  1. Classify each and give its arrow: KOH, H₂CO₃, HI, NH₃.
  2. Why is a 12 M solution of acetic acid still called a weak acid, while very dilute HBr is strong?

Every dissolved ion here carries a definite charge, and the strong lists say which solutes actually deliver those ions. The oxidation number extends that charge bookkeeping to every atom in any formula, ionic or not, and it tracks the electron transfers behind redox reactions.

Dr. Karmach

7 · Oxidation Numbers

Assign oxidation numbers by the priority rules, and find any element the rules skip by setting the sum equal to the species' charge.

Dr. Karmach

Rust, bleach, and batteries

A nail rusts. Bleach lifts a stain. A battery lights a bulb. In each change, atoms give electrons to other atoms. A number on each atom keeps count.

Dr. Karmach

Charges in a formula sum to zero

Fe₂O₃ → iron(III) oxide
three O²⁻: 3(−2) = −6 · split over two Fe: 6 ÷ 2 = 3+ each · 2(+3) + 3(−2) = 0 ✓

Naming rust used this sum: the oxide charges set iron's charge. Oxidation numbers run the same sum on every atom, even in molecules such as CO₂, where no atom is a real ion.

Dr. Karmach

The oxidation number

H₂O → H: +1 · O: −2
2(+1) + 1(−2) = 0 ✓ · the numbers sum to the compound's charge

An atom's oxidation number is the charge it would carry if the shared electrons were assigned by rule. The rules form a priority list. One check governs every assignment: the numbers sum to the species' charge.

Dr. Karmach

The rules, in priority order

The list is one idea: assign shared electrons to the more electronegative atom. O nearly always wins, hence −2; a metal never beats H, so NaH's H is −1.

Dr. Karmach

Oxidation number and ionic charge

Ca²⁺ → oxidation number +2
a monatomic ion: the number is the ion's real charge
CO₂ → C: +4 · O: −2 each
4 + 2(−2) = 0 ✓ · no C⁴⁺ ion here; the atoms share electrons

A monatomic ion's oxidation number is its charge. In a molecule, no atom holds a full charge; the number records assigned electrons. It is written sign-first: +4, not 4+.

Dr. Karmach

What the sum must equal

A neutral compound's numbers sum to zero. A polyatomic ion's numbers sum to the charge written on the ion, never to zero. The target changes; the rules never do.

Dr. Karmach

The method

  1. Assign the known numbers. The first rule that applies wins.
  2. Multiply by the subscripts.
  3. Set the sum equal to the charge. Neutral compound: 0. Polyatomic ion: its charge.
  4. Solve for the unknown.
Dr. Karmach

One route for every oxidation number

Every problem runs the same four steps. The rule cards supply the known numbers; the species' charge sets the target. A solution lights only the cards it used.

Dr. Karmach

Guided example: CH₄

CH₄
given: a neutral compound · wanted: every oxidation number

Natural gas is mostly methane. Assign an oxidation number to each element.

Dr. Karmach

Guided example: solution

CH₄
given: a neutral compound · wanted: every oxidation number

Step 1 · Assign the known numbers

Hydrogen's rule gives +1. Carbon has no rule of its own: call it x.

Dr. Karmach

Guided example: solution

CH₄
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge

Four H atoms contribute 4(+1) = +4. Methane is neutral, so the sum is 0.

x + 4(+1) = 0
C: x · H: +1 each, 4 atoms → +4 · neutral → sum 0
Dr. Karmach

Guided example: solution

CH₄
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 4(+1) = 0
C: x · H: +1 each, 4 atoms → +4 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 − 4 = −4
C: −4 · H: +1 ×4 · check: −4 + 4(+1) = 0 ✓
Dr. Karmach

Guided example: solution

CH₄
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 4(+1) = 0
C: x · H: +1 each, 4 atoms → +4 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 − 4 = −4
C: −4 · H: +1 ×4 · check: −4 + 4(+1) = 0 ✓
H holds the positive side, so C balances from the negative side. The unknown can land negative.
Dr. Karmach

Guided example: the route on the map

CH₄ → C: −4 · H: +1
found: x + 4(+1) = 0 · neutral → sum 0

Only the H card applied. C had no rule, so the sum to 0 set its number. ✓
Dr. Karmach

Worked example 1: SO₂

SO₂
given: a neutral compound · wanted: every oxidation number

Sulfur dioxide forms when coal burns. Assign an oxidation number to each element.

Dr. Karmach

Worked example 1: solution

SO₂
given: a neutral compound · wanted: every oxidation number

Step 1 · Assign the known numbers

Oxygen's rule gives −2. Sulfur has no rule of its own: call it x.

Dr. Karmach

Worked example 1: solution

SO₂
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge

Two O atoms contribute 2(−2) = −4. The compound is neutral, so the sum is 0.

x + 2(−2) = 0
S: x · O: −2 each, 2 atoms → −4 · neutral → sum 0
Dr. Karmach

Worked example 1: solution

SO₂
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 2(−2) = 0
S: x · O: −2 each, 2 atoms → −4 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 + 4 = +4
S: +4 · O: −2, −2 · check: +4 + 2(−2) = 0 ✓
Dr. Karmach

Worked example 1: solution

SO₂
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 2(−2) = 0
S: x · O: −2 each, 2 atoms → −4 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 + 4 = +4
S: +4 · O: −2, −2 · check: +4 + 2(−2) = 0 ✓
The numbers sum to 0, a neutral compound's charge. No S⁴⁺ ion exists in SO₂; +4 records assigned electrons, not a real charge.
Dr. Karmach

Worked example 1: the route on the map

SO₂ → S: +4 · O: −2
found: x + 2(−2) = 0 · neutral → sum 0

The O card gave the known numbers. S took what the sum to 0 required. ✓
Dr. Karmach

Worked example 2: KMnO₄

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn

Potassium permanganate is a deep purple disinfectant. Two of its three elements have rules. Find the oxidation number of Mn.

Dr. Karmach

Worked example 2: solution

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn

Step 1 · Assign the known numbers

Potassium is Group 1: +1. Oxygen's rule gives −2. Manganese has no rule of its own: call it x.

Dr. Karmach

Worked example 2: solution

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge

Four O atoms contribute 4(−2) = −8. The compound is neutral, so the sum is 0.

(+1) + x + 4(−2) = 0
K: +1 · Mn: x · O: −2 each, 4 atoms → −8 · neutral → sum 0
Dr. Karmach

Worked example 2: solution

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
(+1) + x + 4(−2) = 0
K: +1 · Mn: x · O: −2 each, 4 atoms → −8 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 − 1 + 8 = +7
K: +1 · Mn: +7 · O: −2 ×4 · check: +1 + 7 + 4(−2) = 0 ✓
Dr. Karmach

Worked example 2: solution

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
(+1) + x + 4(−2) = 0
K: +1 · Mn: x · O: −2 each, 4 atoms → −8 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 − 1 + 8 = +7
K: +1 · Mn: +7 · O: −2 ×4 · check: +1 + 7 + 4(−2) = 0 ✓
+1 + 7 − 8 = 0 ✓. An element without a rule of its own gets its number from the sum.
Dr. Karmach

Worked example 2: the route on the map

KMnO₄ → K: +1 · Mn: +7 · O: −2
found: 1 + x + 4(−2) = 0 · neutral → sum 0

Two rule cards applied: Group 1 for K, and O. Mn took what the sum to 0 required. ✓
Dr. Karmach

Your turn: H₂SO₄

H₂SO₄
given: a neutral compound · wanted: the oxidation number of S
step work
1 · assign the known numbers H: +1 · O: −2 · S: x
2 · multiply by the subscripts 2(+1) = +2 · 4(−2) =
3 · set the sum equal to the charge +2 + x + (−8) =
4 · solve for the unknown x =

Complete the table.

Dr. Karmach

Your turn: H₂SO₄

H₂SO₄
given: a neutral compound · wanted: the oxidation number of S
step work
1 · assign the known numbers H: +1 · O: −2 · S: x
2 · multiply by the subscripts 2(+1) = +2 · 4(−2) =
3 · set the sum equal to the charge +2 + x + (−8) =
4 · solve for the unknown x =

Complete the table.

2(+1) + x + 4(−2) = 0 → x = +6
H: +1, +1 · S: +6 · O: −2 ×4 · check: +2 + 6 − 8 = 0 ✓
Dr. Karmach

Practice 1

CaSO₃
calcium sulfite · a neutral compound

Power plants trap SO₂ from smoke with lime, which turns it into calcium sulfite. What is the oxidation number of S in CaSO₃?

  1. +6
  2. −2
  3. +5
  4. +4
  5. 0
Dr. Karmach

Practice 1: answer D

(+2) + x + 3(−2) = 0 → x = 0 − 2 + 6 = +4 (answer D)
Ca: +2 (Group 2) · S: +4 · O: −2 ×3 · check: +2 + 4 − 6 = 0 ✓

A left out calcium: x + 3(−2) = 0 gives +6, and +2 + 6 − 6 = +2, not 0. B gave S the sulfite ion's charge, −2; that charge belongs to the whole SO₃ group. C gave Ca Group 1's +1: +1 + x − 6 = 0 → +5, but Ca sits in Group 2. E counted the −2 once: +2 + x − 2 = 0 → 0; three O atoms contribute −6.

Dr. Karmach

Practice 1: answer D

(+2) + x + 3(−2) = 0 → x = 0 − 2 + 6 = +4 (answer D)
Ca: +2 (Group 2) · S: +4 · O: −2 ×3 · check: +2 + 4 − 6 = 0 ✓
S is +4 in both SO₂ and CaSO₃. Trapping the gas changed its partners, not its number. ✓

Dr. Karmach

Where this goes wrong

Counting the −2 once for the whole formula. In CO₃²⁻, x + (−2) = −2 gives x = 0. The −2 belongs to each O atom: three of them contribute 3(−2) = −6, and x + (−6) = −2 gives x = +4.
Putting the unknown on the negative side. In ClO₃⁻, writing Cl as −5 sums to −5 − 6 = −11, not −1. Oxygen already holds the negative numbers; Cl balances them from the positive side: −1 + 6 = +5.
Giving H +1 next to a metal. In NaH, that reads +1 + 1 = +2, not 0. Sodium's rule sits higher on the list, so Na is +1 and H takes −1: +1 − 1 = 0 ✓.
Giving O −2 in a peroxide. In H₂O₂, that reads 2(+1) + 2(−2) = −2, not 0. Peroxide oxygen is −1: 2(+1) + 2(−1) = 0 ✓.
Dr. Karmach

Worked example 3: SO₄²⁻

Step 1 · Assign the known numbers

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S

The sulfate ion appears in fertilizer and hard water. A common first attempt sets the sum to zero. Test it.

Dr. Karmach

Worked example 3: testing the first attempt

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S

A common first attempt

x + 4(−2) = 0 → x = +8
sum: +8 − 8 = 0 ✗, but SO₄²⁻ is not neutral
Dr. Karmach

Worked example 3: testing the first attempt

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S

A common first attempt

x + 4(−2) = 0 → x = +8
sum: +8 − 8 = 0 ✗, but SO₄²⁻ is not neutral
A sum of zero describes a neutral species. This ion carries 2−.
The check must land on the charge written on the species: −2, not 0.
Dr. Karmach

Worked example 3: solution

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S

Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge

Four O atoms contribute 4(−2) = −8. The species is an ion, so the sum is its charge: −2.

x + 4(−2) = −2
S: x · O: −2 each, 4 atoms → −8 · ion → sum −2, not 0
Dr. Karmach

Worked example 3: solution

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S
Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 4(−2) = −2
S: x · O: −2 each, 4 atoms → −8 · ion → sum −2, not 0
Step 4 · Solve for the unknown
x = −2 + 8 = +6
S: +6 · O: −2 ×4 · check: +6 − 8 = −2 ✓, the ion's charge
Dr. Karmach

Worked example 3: solution

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S
Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 4(−2) = −2
S: x · O: −2 each, 4 atoms → −8 · ion → sum −2, not 0
Step 4 · Solve for the unknown
x = −2 + 8 = +6
S: +6 · O: −2 ×4 · check: +6 − 8 = −2 ✓, the ion's charge
+6 − 8 = −2 ✓. The first attempt's +8 fails the same check: +8 − 8 = 0 ≠ −2.
Dr. Karmach

Worked example 3: the route on the map

SO₄²⁻ → S: +6 · O: −2
found: x + 4(−2) = −2 · ion → sum −2

Same O card as SO₂. The ion card moved the target from 0 to −2. ✓
Dr. Karmach

Practice 2

C₂O₄²⁻
the oxalate ion · a polyatomic ion

Spinach and rhubarb leaves hold the oxalate ion. What is the oxidation number of each C atom in C₂O₄²⁻?

  1. +3
  2. +4
  3. +5
  4. +6
Dr. Karmach

Practice 2: answer A

2x + 4(−2) = −2 → 2x = −2 + 8 = 6 → x = +3 (answer A)
C: +3 each, 2 atoms → +6 · O: −2 ×4 → −8 · check: +6 − 8 = −2 ✓, the ion's charge

B set the sum to zero: 2x − 8 = 0 → +4, and 2(+4) − 8 = 0 ≠ −2. C used +2 for the 2− charge: 2x − 8 = +2 → +5. D dropped the subscript on C: x − 8 = −2 → +6, but two C atoms at +6 sum to 12 − 8 = +4.

Dr. Karmach

Practice 2: answer A

2x + 4(−2) = −2 → 2x = −2 + 8 = 6 → x = +3 (answer A)
C: +3 each, 2 atoms → +6 · O: −2 ×4 → −8 · check: +6 − 8 = −2 ✓, the ion's charge
Two alike C atoms share +6 equally: +3 each. The sum lands on the ion's charge, −2. ✓

Dr. Karmach

Practice 3

NH₃ · NH₄⁺
ammonia, a neutral molecule · ammonium, a polyatomic ion

Fertilizer plants turn ammonia into ammonium salts. Compare the oxidation number of N in the two species. Which statement is correct?

  1. Different: −3 in NH₃ but −4 in NH₄⁺.
  2. The same in both: −3. The sums differ, 0 and +1, yet both solve to −3.
  3. In NH₄⁺, N simply carries the ion's charge, +1; only in NH₃ is it −3.
  4. The same in both: +3, since the central atom takes the positive side.
Dr. Karmach

Practice 3: answer B

NH₃: x + 3(+1) = 0 → x = 0 − 3 = −3
H: +1 (rule) · a neutral molecule: the sum's target is 0 · check: −3 + 3 = 0 ✓
NH₄⁺: x + 4(+1) = +1 → x = 1 − 4 = −3 (answer B)
a polyatomic ion: the sum's target is its charge, +1 · check: −3 + 4 = +1 ✓

A set the ion's sum to zero: x + 4 = 0 gives −4, and −4 + 4 = 0 ≠ +1. C gave N the ion's charge; that shortcut holds only for a monatomic ion. D flipped the sign: +3 + 3(+1) = +6, not 0. H already holds the positive side, so N balances from the negative side.

Dr. Karmach

Practice 3: answer B

NH₃: x + 3(+1) = 0 → x = 0 − 3 = −3
H: +1 (rule) · a neutral molecule: the sum's target is 0 · check: −3 + 3 = 0 ✓
NH₄⁺: x + 4(+1) = +1 → x = 1 − 4 = −3 (answer B)
a polyatomic ion: the sum's target is its charge, +1 · check: −3 + 4 = +1 ✓
Different targets, same rules, same answer. The extra H in NH₄⁺ brought its own +1, and the ion's charge absorbs it.

Dr. Karmach

Take-home: an ion's numbers sum to the ion's charge

H₂SO₄: 2(+1) + 6 + 4(−2) = 0
a neutral compound · the sum's target is 0
SO₄²⁻: 6 + 4(−2) = −2
a polyatomic ion · the sum's target is the charge written on the ion

Zero is reserved for neutral species. Both give S +6: the target changes, not the rules.

Dr. Karmach

Practice 4

PO₄³⁻
the phosphate ion · O: −2 each (rule) · P: x

Fertilizer supplies phosphorus as the phosphate ion. What is the oxidation number of P in PO₄³⁻?

  1. +8
  2. −5
  3. +5
  4. −1
Dr. Karmach

Practice 4: answer C

x + 4(−2) = −3 → x = −3 + 8 = +5 (answer C)
P: +5 · O: −2 ×4 · check: +5 − 8 = −3 ✓, the ion's charge

A set the sum to zero: x + 4(−2) = 0 → +8. B put the unknown on the negative side: −5 − 8 = −13, not −3. D counted the −2 once for the whole ion: x + (−2) = −3 → −1; four O atoms contribute −8.

Dr. Karmach

Practice 4: answer C

x + 4(−2) = −3 → x = −3 + 8 = +5 (answer C)
P: +5 · O: −2 ×4 · check: +5 − 8 = −3 ✓, the ion's charge
+5 − 8 = −3 ✓. A 3− ion's numbers must sum to −3.

Dr. Karmach

Check yourself

  1. Assign every oxidation number in Na₂CrO₄. Which element's number comes from the sum?
  2. In NO₃⁻, what must the numbers sum to, and what number does N carry?

When a reaction runs, these numbers can change. An element whose number rises has lost electrons; one whose number falls has gained them. Those changes mark oxidation and reduction, and the reactants that cause them are the oxidizing and reducing agents.

Dr. Karmach

8 · Oxidizing & Reducing Agents

Decide from oxidation-number changes whether a reaction is redox, tell what is oxidized and what is reduced, and name the oxidizing and reducing agents.

Dr. Karmach

Silver grows on copper

A copper wire stands overnight in dissolved silver. Solid silver collects on the wire; the liquid turns blue with dissolved copper. The two metals have traded places.

Dr. Karmach

Electrons never vanish

Some reactions move electrons from one substance to another. Every electron one atom loses, another atom gains. Oxidation numbers make the transfer visible: they change only where electrons leave or arrive.

Dr. Karmach

Ion charges are oxidation numbers

2 Na + Cl₂ → 2 NaCl
sodium metal + chlorine gas → table salt, made of Na⁺ and Cl⁻ ions
Na: 0 → +1, gave 1 e⁻ · Cl: 0 → −1, took 1 e⁻
2 Na give 2 e⁻ · 2 Cl take 2 e⁻ · NaCl: (+1) + (−1) = 0

An element by itself counts 0. A simple ion's charge is its oxidation number. Forming an ion moves electrons: sodium gave one away, chlorine took it.

Dr. Karmach

Oxidation and reduction

oxidation = the oxidation number increases: electrons lost
Zn + Cu²⁺ → Zn²⁺ + Cu · Zn: 0 → +2 · zinc is oxidized
reduction = the oxidation number decreases: electrons gained
Zn + Cu²⁺ → Zn²⁺ + Cu · Cu: +2 → 0 · copper is reduced

Assign oxidation numbers to both sides and compare. Electrons are negative, so losing them pushes the number up and gaining them pulls it down. OIL RIG: Oxidation Is Loss, Reduction Is Gain.

Dr. Karmach

Naming the agents

Each agent is named for what it does to its partner, not for what happens to itself. Both agents are reactants: name the whole substance, not just the atom.

Dr. Karmach

The method

  1. Assign oxidation numbers to every atom, both sides.
  2. Find the changes: an increase is oxidation, a decrease is reduction.
  3. Name the agents: the reduced atom's reactant is the oxidizing agent; the oxidized atom's is the reducing agent.

Dr. Karmach

Guided example: iron and sulfur

Step 1 · Assign oxidation numbers

Fe + S → FeS
Fe: 0 → +2 · S: 0 → −2

Iron filings heated with sulfur glow red and leave a black solid, iron(II) sulfide. Fe and S alone count 0. In FeS, sulfur is the sulfide ion, −2; iron balances the formula: x + (−2) = 0 gives +2.

Which element is oxidized, which is reduced, and which reactant is each agent?

Dr. Karmach

Guided example: solution

Fe + S → FeS
Fe: 0 → +2 · S: 0 → −2

Step 2 · Find the changes

Fe rises 0 → +2: iron is oxidized, losing 2 electrons. S falls 0 → −2: sulfur is reduced, gaining 2 electrons.

Dr. Karmach

Guided example: solution

Fe + S → FeS
Fe: 0 → +2 · S: 0 → −2
Step 2 · Find the changes Step 3 · Name the agents

Fe gave its electrons to S: Fe is the reducing agent. S took them: S is the oxidizing agent.

Electrons lost = gained: Fe lost 2, S gained 2. Each agent sits at the end of its own atom's lane. ✓

Dr. Karmach

Worked example 1: zinc in copper(II) sulfate

Step 1 · Assign oxidation numbers

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2 · Cu: +2 → 0 · S: +6 → +6 · O: −2 → −2

A zinc strip in blue copper(II) sulfate solution darkens with copper, a single-displacement reaction. Elements by themselves count 0; O is −2; sulfate's sum, x + 4(−2) = −2, gives S +6; Cu balances its neutral formula at +2.

Which element is oxidized, and which is reduced?

Dr. Karmach

Worked example 1: solution

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2 · Cu: +2 → 0 · S: +6 → +6 · O: −2 → −2

Step 2 · Find the changes

Zn increases, 0 → +2: zinc is oxidized. It lost 2 electrons. Cu decreases, +2 → 0: copper is reduced. It gained 2 electrons.

Dr. Karmach

Worked example 1: solution

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2 · Cu: +2 → 0 · S: +6 → +6 · O: −2 → −2
Step 2 · Find the changes The unchanged atoms

S stays +6 and O stays −2. The sulfate group moves as one piece; no atom in it loses or gains anything. The transfer runs between Zn and Cu only.

Dr. Karmach

Worked example 1: solution

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2 · Cu: +2 → 0 · S: +6 → +6 · O: −2 → −2
Step 2 · Find the changes The unchanged atoms
Electrons lost = electrons gained: Zn lost 2, Cu gained 2. A reaction cannot lose electrons without something gaining them.

Dr. Karmach

Worked example 2: copper in silver nitrate

Step 1 · Assign oxidation numbers

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2

A copper wire in silver nitrate solution grows silver crystals while the liquid turns blue. Elements count 0; O is −2; nitrate's sum, x + 3(−2) = −1, gives N +5; Ag and Cu balance their formulas at +1 and +2.

Name both agents. A common first answer: copper is oxidized, so copper is the oxidizing agent. Test it against the definitions.

Dr. Karmach

Worked example 2: solution

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2

Step 2 · Find the changes

Cu increases, 0 → +2: copper is oxidized, losing 2 electrons. Ag decreases, +1 → 0: silver is reduced, each atom gaining 1 electron. N and O do not change.

Dr. Karmach

Worked example 2: solution

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2
Step 2 · Find the changes A common first answer

Copper is oxidized. That does not make it the oxidizing agent: the name describes what a reactant does to its partner. Copper gives its electrons away and oxidizes nothing. The silver in AgNO₃ takes them, so AgNO₃ does the oxidizing.

Dr. Karmach

Worked example 2: solution

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2
Step 2 · Find the changes A common first answer Step 3 · Name the agents
agent substance evidence
oxidizing agent AgNO₃ contains Ag, reduced +1 → 0
reducing agent Cu oxidized 0 → +2
Dr. Karmach

Worked example 2: solution

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2
Step 2 · Find the changes A common first answer Step 3 · Name the agents
agent substance evidence
oxidizing agent AgNO₃ contains Ag, reduced +1 → 0
reducing agent Cu oxidized 0 → +2
The oxidized lane ends at the reducing agent: oxidized copper is the reducing agent. ✓

Dr. Karmach

Take-home: the oxidized substance is the reducing agent

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2, oxidized · Cu: +2 → 0, reduced · S and O unchanged
reducing agent: Zn · oxidizing agent: CuSO₄
the oxidized substance gave the electrons · the reduced atom's reactant took them

An agent's name tells what it does to its partner. The oxidized substance gives electrons: the reducing agent. The reduced substance takes them: the oxidizing agent.

Dr. Karmach

Your turn: magnesium in hydrochloric acid

Mg + 2 HCl → MgCl₂ + H₂
Mg: 0 → · H: +1 → · Cl: −1 → −1
question answer
oxidized / reduced
oxidizing agent
reducing agent

Complete the two changes, then name both agents.

Dr. Karmach

Your turn: magnesium in hydrochloric acid

Mg + 2 HCl → MgCl₂ + H₂
Mg: 0 → · H: +1 → · Cl: −1 → −1
question answer
oxidized / reduced
oxidizing agent
reducing agent

Complete the two changes, then name both agents.

Mg + 2 HCl → MgCl₂ + H₂
Mg: 0 → +2 (oxidized) · H: +1 → 0 (reduced) · Cl: −1 → −1 unchanged · e⁻: 2 lost = 2 gained ✓

HCl contains the reduced H: the oxidizing agent. Mg is oxidized: the reducing agent.

Dr. Karmach

Where this goes wrong

Swapping the two agents. In Zn + CuSO₄ → ZnSO₄ + Cu, calling Zn the oxidizing agent and CuSO₄ the reducing agent reverses both names. CuSO₄ takes zinc's electrons, and the reactant that takes electrons does the oxidizing. No metal is required for that job: in Cl₂ + 2 KBr → 2 KCl + Br₂, the bare nonmetal Cl₂ takes bromide's electrons and is the oxidizing agent.
Calling the oxidized substance the oxidizing agent. Being oxidized means giving electrons to the partner, and giving electrons is what reduces the partner. The oxidized substance is always the reducing agent.
Picking a spectator as the agent. In Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag, nitrate moves from silver to copper, yet N stays +5 and O stays −2. Changing partners moves no electrons. Agents contain atoms whose numbers change.
Dr. Karmach

Practice 1

Ni + CuCl₂ → NiCl₂ + Cu

A nickel bar sits in green copper(II) chloride solution and slowly plates with copper. Which species is the oxidizing agent?

  1. Ni, because it is the species that gets oxidized.
  2. CuCl₂, because it contains Cu, which is reduced from +2 to 0.
  3. The chloride ion, Cl⁻: it changes partners during the reaction, so it drives the electron transfer.
  4. Ni is the oxidizing agent, and CuCl₂ is the reducing agent.
Dr. Karmach

Practice 1: answer B

Ni + CuCl₂ → NiCl₂ + Cu
Ni: 0 → +2 (oxidized) · Cu: +2 → 0 (reduced) · Cl: −1 → −1 unchanged
Cu: +2 → 0 · reduced · its reactant is CuCl₂ = the oxidizing agent (answer B)

A named the oxidized species: losing electrons to the partner is exactly what makes Ni the reducing agent. C followed the partner-swapping: Cl is −1 on both sides, a change of (−1) − (−1) = 0, so chloride transferred nothing. D swapped both names: CuCl₂ takes nickel's electrons, and the taker does the oxidizing.

Dr. Karmach

Practice 1: answer B

Ni + CuCl₂ → NiCl₂ + Cu
Ni: 0 → +2 (oxidized) · Cu: +2 → 0 (reduced) · Cl: −1 → −1 unchanged
Cu: +2 → 0 · reduced · its reactant is CuCl₂ = the oxidizing agent (answer B)
Electrons lost = gained: Ni lost 2, Cu gained 2. ✓

Dr. Karmach

Worked example 3: testing whether a reaction is redox

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃

Two colorless solutions mix and a bright yellow solid, PbI₂, appears. Every formula changes partners.

Assign oxidation numbers to both sides: is any element oxidized or reduced?

Dr. Karmach

Worked example 3: solution

Step 1 · Assign oxidation numbers

K, a group 1A metal, is +1; the iodide ion is −1; O is −2; nitrate's sum, x + 3(−2) = −1, gives N +5; Pb balances each formula at +2.

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
Pb: +2 → +2 · N: +5 → +5 · O: −2 → −2 · K: +1 → +1 · I: −1 → −1
Dr. Karmach

Worked example 3: solution

Step 1 · Assign oxidation numbers

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
Pb: +2 → +2 · N: +5 → +5 · O: −2 → −2 · K: +1 → +1 · I: −1 → −1
Step 2 · Find the changes

Every number is the same on both sides. Nothing is oxidized and nothing is reduced: no electrons moved. This reaction is not redox, and it has no oxidizing or reducing agent.

Dr. Karmach

Worked example 3: solution

Step 1 · Assign oxidation numbers

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
Pb: +2 → +2 · N: +5 → +5 · O: −2 → −2 · K: +1 → +1 · I: −1 → −1
Step 2 · Find the changes
Electrons lost = gained: 0 = 0. A yellow precipitate is a real reaction, but ions that keep their numbers have only changed partners.

Dr. Karmach

Half-reactions

oxidation half: X → X⁺ + e⁻
the electron is a product: X lost it · LEO, Lose Electrons: Oxidation
reduction half: Y⁺ + e⁻ → Y
the electron is a reactant: Y⁺ gained it · GER, Gain Electrons: Reduction

Any redox reaction splits into two half-reactions, the loss and the gain written separately. Each half must balance atoms and total charge. LEO GER and OIL RIG state the same rule.

Dr. Karmach

Worked example 4: splitting a reaction into half-reactions

Zn(s) + Cu²⁺(aq) → Zn²⁺(aq) + Cu(s)
Zn: 0 → +2 · Cu: +2 → 0 · wanted: both half-reactions, classified

A zinc strip in copper(II) solution, written as a net ionic equation. Split the reaction into its two half-reactions, classify each, and check that the electron counts match.

Dr. Karmach

Worked example 4: solution

Zn(s) + Cu²⁺(aq) → Zn²⁺(aq) + Cu(s)
Zn: 0 → +2 · Cu: +2 → 0

The oxidation half-reaction

Zn rises 0 → +2: it lost 2 electrons. Lost electrons are written as a product.

Zn → Zn²⁺ + 2 e⁻
atoms: Zn 1 = 1 ✓ · charge: left 0 · right (2+) + 2(1−) = 0 ✓
Dr. Karmach

Worked example 4: solution

Zn(s) + Cu²⁺(aq) → Zn²⁺(aq) + Cu(s)
Zn: 0 → +2 · Cu: +2 → 0
The oxidation half-reaction
Zn → Zn²⁺ + 2 e⁻
atoms: Zn 1 = 1 ✓ · charge: left 0 · right (2+) + 2(1−) = 0 ✓
The reduction half-reaction

Cu falls +2 → 0: it gained 2 electrons. Gained electrons are written as a reactant.

Cu²⁺ + 2 e⁻ → Cu
atoms: Cu 1 = 1 ✓ · charge: left (2+) + 2(1−) = 0 · right 0 ✓
Dr. Karmach

Worked example 4: solution

Zn(s) + Cu²⁺(aq) → Zn²⁺(aq) + Cu(s)
Zn: 0 → +2 · Cu: +2 → 0
The oxidation half-reaction
Zn → Zn²⁺ + 2 e⁻
atoms: Zn 1 = 1 ✓ · charge: left 0 · right (2+) + 2(1−) = 0 ✓
The reduction half-reaction
Cu²⁺ + 2 e⁻ → Cu
atoms: Cu 1 = 1 ✓ · charge: left (2+) + 2(1−) = 0 · right 0 ✓
2 e⁻ leave the oxidation half and 2 e⁻ enter the reduction half: lost = gained. Adding the halves cancels the electrons and rebuilds the equation.
Dr. Karmach

Practice 2

2 FeCl₂ + Cl₂ → 2 FeCl₃

Chlorine bubbled through pale green iron(II) chloride solution turns it yellow-brown. Which reactant is the reducing agent, and how many electrons change hands in the equation as written?

  1. Cl₂ is the reducing agent; 2 electrons change hands.
  2. FeCl₂ is the reducing agent; 4 electrons change hands.
  3. FeCl₂ is the reducing agent; 1 electron changes hands.
  4. FeCl₂ is the reducing agent; 2 electrons change hands.
Dr. Karmach

Practice 2: answer D

2 FeCl₂ + Cl₂ → 2 FeCl₃
Fe: +2 → +3 (oxidized) · Cl from Cl₂: 0 → −1 (reduced) · Cl already in FeCl₂: −1 → −1
2 Fe × 1 e⁻ lost = 2 e⁻ = 2 Cl × 1 e⁻ gained · FeCl₂ gives them: the reducing agent (answer D)

Fe comes from the sums: x + 2(−1) = 0 gives +2; x + 3(−1) = 0 gives +3. A swapped the names: Cl₂ takes iron's electrons, and the taker is the oxidizing agent. B added lost to gained, 2 + 2 = 4; they are the same 2 electrons, changing hands once. C counted one Fe atom, 3 − 2 = 1 e⁻, but the equation oxidizes 2 Fe.

Dr. Karmach

Practice 2: answer D

2 FeCl₂ + Cl₂ → 2 FeCl₃
Fe: +2 → +3 (oxidized) · Cl from Cl₂: 0 → −1 (reduced) · Cl already in FeCl₂: −1 → −1
2 Fe × 1 e⁻ lost = 2 e⁻ = 2 Cl × 1 e⁻ gained · FeCl₂ gives them: the reducing agent (answer D)
Chlorine stands on both sides, yet only the two Cl atoms from Cl₂ change. Lost = gained: 2 = 2 ✓.

Dr. Karmach

Practice 3

Al + 3 AgNO₃ → Al(NO₃)₃ + 3 Ag

Aluminum foil in silver nitrate solution slowly coats with silver. Which half-reaction belongs to the reducing agent?

  1. Ag⁺ + e⁻ → Ag
  2. Al + 3 e⁻ → Al³⁺
  3. Al → Al³⁺ + e⁻
  4. Al³⁺ + 3 e⁻ → Al
  5. Al → Al³⁺ + 3 e⁻
Dr. Karmach

Practice 3: answer E

Al + 3 AgNO₃ → Al(NO₃)₃ + 3 Ag
Al: 0 → +3 (oxidized) · Ag: +1 → 0 (reduced) · N: +5 → +5 · O: −2 → −2
Al: 0 → +3 · oxidized: the reducing agent · 3 e⁻ lost, a product = Al → Al³⁺ + 3 e⁻ (answer E)

A is the other half: Ag⁺ gains the electrons, so it belongs to AgNO₃, the oxidizing agent. B put lost electrons on the gain side: left 0 + 3(1−) = −3, right 3+. C copied one silver's single electron: right (3+) + 1(1−) = +2, not 0. D balances, (3+) + 3(1−) = 0, but runs backward: Al³⁺ is made here, not used.

Dr. Karmach

Practice 3: answer E

Al + 3 AgNO₃ → Al(NO₃)₃ + 3 Ag
Al: 0 → +3 (oxidized) · Ag: +1 → 0 (reduced) · N: +5 → +5 · O: −2 → −2
Al: 0 → +3 · oxidized: the reducing agent · 3 e⁻ lost, a product = Al → Al³⁺ + 3 e⁻ (answer E)
Electrons lost = gained: 1 Al × 3 e⁻ = 3 Ag × 1 e⁻ = 3. Charge: left 0, right (3+) + 3(1−) = 0 ✓

Dr. Karmach

Practice 4: halogens

Cl₂ + 2 KBr → 2 KCl + Br₂

Chlorine gas bubbled through potassium bromide solution turns it orange with bromine. Which species is the oxidizing agent?

  1. KBr, because it is the species that gets oxidized.
  2. The potassium ion, K⁺: it changes partners during the reaction, so it drives the electron transfer.
  3. Cl₂, because it contains Cl, which is reduced from 0 to −1.
  4. KBr is the oxidizing agent, and Cl₂ is the reducing agent.
Dr. Karmach

Practice 4: answer C

Cl₂ + 2 KBr → 2 KCl + Br₂
Cl: 0 → −1 (reduced) · Br: −1 → 0 (oxidized) · K: +1 → +1 unchanged
Cl: 0 → −1 · reduced · its reactant is Cl₂ = the oxidizing agent (answer C)

A named the oxidized species: KBr gives its electrons away, which makes it the reducing agent. B followed the partner-swapping: K is +1 in KBr and +1 in KCl, a change of 1 − 1 = 0. D swapped both names: Cl₂ takes bromide's electrons, and the taker does the oxidizing. An oxidizing agent need not contain a metal.

Dr. Karmach

Practice 4: answer C

Cl₂ + 2 KBr → 2 KCl + Br₂
Cl: 0 → −1 (reduced) · Br: −1 → 0 (oxidized) · K: +1 → +1 unchanged
Cl: 0 → −1 · reduced · its reactant is Cl₂ = the oxidizing agent (answer C)
Electrons lost = gained: 2 Br × 1 e⁻ = 2 lost; 2 Cl × 1 e⁻ = 2 gained. ✓

Dr. Karmach

Reference: common oxidizing and reducing agents

common oxidizing agents: F₂ · Cl₂ · O₂ · MnO₄⁻ · Cr₂O₇²⁻ · H₂O₂
electron takers: each holds an atom whose oxidation number is ready to fall
common reducing agents: elemental metals (Zn, Al, Fe, Na) · H₂ · Fe²⁺ · I⁻
electron givers: each holds an atom whose oxidation number is ready to rise

The same substances turn up in reaction after reaction. A reference for recognition only: assigning oxidation numbers still decides every specific case.

Dr. Karmach

Check yourself

  1. In Fe + CuSO₄ → FeSO₄ + Cu, iron goes 0 → +2. Which reactant is the reducing agent, and which element took iron's electrons?
  2. Split Zn + 2 HCl → ZnCl₂ + H₂ into its two half-reactions. Which half carries the electrons as a reactant?

Redox is an electron hand-off: one substance gives, the other takes. Whether a particular metal pair actually trades is decided by a ranking of metals, the activity series.

Dr. Karmach

9 · The Activity Series

Use the activity series to predict whether a single-displacement reaction runs, write the products when it does, and write no reaction when it does not.

Dr. Karmach

Two metals, one acid

Zinc fizzes furiously in hydrochloric acid; copper sits in the same acid untouched, forever. Something ranks these metals.

Dr. Karmach

The activity series

Four tiers, ranked by how readily each metal gives electrons away: displace any cation below you, never one above.

Dr. Karmach

Two guaranteed product patterns

metal + acid → salt + H₂(g)
any metal above hydrogen pushes its electrons onto H⁺
active metal + water → metal hydroxide + H₂(g)
the cold-water tier takes its hydrogen from water itself

The series is a measured ranking of how readily each metal gives its electrons away. A metal above hydrogen runs its oxidation half-reaction against H⁺, and the products follow the pattern.

Dr. Karmach

The method

  1. Find both metals in the series. With acid or water, hydrogen is the second metal.
  2. Compare positions. The solid metal must sit above its partner; otherwise write no reaction.
  3. Write the products from the pattern.
  4. Balance the equation.
Dr. Karmach

Worked example 1: magnesium in hydrochloric acid

Step 1 · Find both metals in the series

Mg(s) + HCl(aq) → ?
Mg: the steam tier · H: supplied by the acid · wanted: products, balanced

A magnesium strip dropped into hydrochloric acid dissolves in a rush of bubbles. Predict the products and balance the equation.

Dr. Karmach

Worked example 1: solution

Mg(s) + HCl(aq) → ?
Mg: the steam tier · H: supplied by the acid

Step 2 · Compare positions

Mg stands above hydrogen. The reaction runs: magnesium hands its electrons to H⁺.

Dr. Karmach

Worked example 1: solution

Mg(s) + HCl(aq) → ?
Mg: the steam tier · H: supplied by the acid
Step 2 · Compare positions Step 3 · Write the products from the pattern

Metal + acid → salt + H₂. Magnesium forms a 2+ ion and chloride is 1−, so the salt is MgCl₂.

Mg + HCl → MgCl₂ + H₂ (skeleton)
charge in the salt: (2+) + 2(1−) = 0 ✓
Dr. Karmach

Worked example 1: solution

Mg(s) + HCl(aq) → ?
Mg: the steam tier · H: supplied by the acid
Step 2 · Compare positions Step 3 · Write the products from the pattern
Mg + HCl → MgCl₂ + H₂ (skeleton)
charge in the salt: (2+) + 2(1−) = 0 ✓
Step 4 · Balance the equation
Mg + 2 HCl → MgCl₂ + H₂
Mg: 1 = 1 ✓ · H: 2 = 2 ✓ · Cl: 2 = 2 ✓
Dr. Karmach

Worked example 1: solution

Mg(s) + HCl(aq) → ?
Mg: the steam tier · H: supplied by the acid
Step 2 · Compare positions Step 3 · Write the products from the pattern
Mg + HCl → MgCl₂ + H₂ (skeleton)
charge in the salt: (2+) + 2(1−) = 0 ✓
Step 4 · Balance the equation
Mg + 2 HCl → MgCl₂ + H₂
Mg: 1 = 1 ✓ · H: 2 = 2 ✓ · Cl: 2 = 2 ✓
The bubbles are the H₂ the pattern promised. Mg loses 2 e⁻; two H⁺ gain 1 each: lost = gained, 2 = 2 ✓.
Dr. Karmach

Worked example 1: the route on the series

Mg + 2 HCl → MgCl₂ + H₂
solid metal: Mg · partner: hydrogen, from the acid · found: the reaction runs

With an acid, the partner is hydrogen. Mg sits above the H₂ line, so the reaction runs. ✓
Dr. Karmach

Worked example 2: aluminum in nickel(II) nitrate

Step 1 · Find both metals in the series

Al(s) + Ni(NO₃)₂(aq) → ?
Al: the steam tier · Ni: the acid tier, lower · wanted: products, balanced

Aluminum foil sits in green nickel(II) nitrate solution and slowly darkens with nickel. Predict the products and balance the equation.

Dr. Karmach

Worked example 2: solution

Al(s) + Ni(NO₃)₂(aq) → ?
Al: the steam tier · Ni: the acid tier, lower

Step 2 · Compare positions

Al stands above Ni. The reaction runs: aluminum displaces the nickel ion from solution.

Dr. Karmach

Worked example 2: solution

Al(s) + Ni(NO₃)₂(aq) → ?
Al: the steam tier · Ni: the acid tier, lower
Step 2 · Compare positions Step 3 · Write the products from the pattern

Aluminum forms a 3+ ion; nitrate is 1−. Three nitrates balance one aluminum, and nickel leaves as the solid metal.

Al + Ni(NO₃)₂ → Al(NO₃)₃ + Ni (skeleton)
charge in the salt: (3+) + 3(1−) = 0 ✓
Dr. Karmach

Worked example 2: solution

Al(s) + Ni(NO₃)₂(aq) → ?
Al: the steam tier · Ni: the acid tier, lower
Step 2 · Compare positions Step 3 · Write the products from the pattern
Al + Ni(NO₃)₂ → Al(NO₃)₃ + Ni (skeleton)
charge in the salt: (3+) + 3(1−) = 0 ✓
Step 4 · Balance the equation
2 Al + 3 Ni(NO₃)₂ → 2 Al(NO₃)₃ + 3 Ni
Al: 2 = 2 ✓ · Ni: 3 = 3 ✓ · N: 3(2) = 6 = 2(3) ✓ · O: 3(6) = 18 = 2(9) ✓
Dr. Karmach

Worked example 2: solution

Al(s) + Ni(NO₃)₂(aq) → ?
Al: the steam tier · Ni: the acid tier, lower
Step 2 · Compare positions Step 3 · Write the products from the pattern
Al + Ni(NO₃)₂ → Al(NO₃)₃ + Ni (skeleton)
charge in the salt: (3+) + 3(1−) = 0 ✓
Step 4 · Balance the equation
2 Al + 3 Ni(NO₃)₂ → 2 Al(NO₃)₃ + 3 Ni
Al: 2 = 2 ✓ · Ni: 3 = 3 ✓ · N: 3(2) = 6 = 2(3) ✓ · O: 3(6) = 18 = 2(9) ✓
Electrons match too: 2 Al lose 3 e⁻ each, 6 total; 3 Ni²⁺ gain 2 each, 6 total. The nitrate ions only change partners.
Dr. Karmach

Worked example 2: the route on the series

2 Al + 3 Ni(NO₃)₂ → 2 Al(NO₃)₃ + 3 Ni
solid metal: Al · partner: Ni, in the compound · found: the reaction runs

Al sits in the steam tier, a full tier above Ni. The higher metal displaces the lower cation. ✓
Dr. Karmach

Your turn: calcium in cold water

Ca(s) + H₂O(l) → ?
the pattern: active metal + water → metal hydroxide + H₂
step work
1 · find both metals Ca: the cold-water tier · H: from the water itself
2 · compare positions Ca sits hydrogen: the reaction runs
3 · products from the pattern Ca(OH)₂ +
4 · balance Ca + H₂O → Ca(OH)₂ + H₂

Complete the table.

Dr. Karmach

Your turn: calcium in cold water

Ca(s) + H₂O(l) → ?
the pattern: active metal + water → metal hydroxide + H₂
step work
1 · find both metals Ca: the cold-water tier · H: from the water itself
2 · compare positions Ca sits hydrogen: the reaction runs
3 · products from the pattern Ca(OH)₂ +
4 · balance Ca + H₂O → Ca(OH)₂ + H₂

Complete the table.

Ca + 2 H₂O → Ca(OH)₂ + H₂
Ca: 1 = 1 ✓ · O: 2 = 2 ✓ · H: 2(2) = 4 = 2 + 2 ✓
Dr. Karmach

Where this goes wrong

Running the series upward. Zinc displaces Cu²⁺, so it is tempting to write the reverse: Cu + ZnSO₄ → CuSO₄ + Zn. Copper sits below zinc and cannot hand its electrons up the list. The reverse of a working displacement never runs.
Never writing "no reaction." Ag + ZnCl₂ swaps neatly on paper into AgCl + Zn, and it never happens: silver sits in the unreactive tier, below zinc. When the solid metal lies below the dissolved cation, no reaction is the complete answer.
Dr. Karmach

Practice 1

Zn(s) + Pb(NO₃)₂(aq) → ?
Zn: the steam tier · Pb: the acid tier, lower

A zinc strip hangs in lead(II) nitrate solution, and gray crystals grow on it. Which equation describes the change?

  1. Zn + Pb(NO₃)₂ → Zn(NO₃)₂ + Pb: zinc, above lead, hands its electrons to Pb²⁺
  2. No reaction: lead sits above zinc, so zinc cannot displace it
  3. Zn + Pb(NO₃)₂ → ZnNO₃ + Pb: the displacement runs, with zinc as a 1+ ion
  4. Both directions run: Pb + Zn(NO₃)₂ → Pb(NO₃)₂ + Zn works just as well
Dr. Karmach

Practice 1: answer A

Zn + Pb(NO₃)₂ → Zn(NO₃)₂ + Pb (answer A)
Zn: 1 = 1 ✓ · Pb: 1 = 1 ✓ · N: 2 = 2 ✓ · O: 6 = 6 ✓ · Zn above Pb: the reaction runs

B reverses the ranking: zinc stands in the steam tier and lead in the acid tier below it. C has the displacement right and the salt wrong: zinc forms a 2+ ion and nitrate is 1−, so the salt is Zn(NO₃)₂, (2+) + 2(1−) = 0. D runs the series upward: lead, the lower metal, never displaces Zn²⁺.

Zn loses 2 e⁻ and Pb²⁺ gains 2: lost = gained ✓. The gray crystals are lead metal leaving the solution.
Dr. Karmach

Worked example 3: copper in lithium nitrate

Step 1 · Find both metals in the series

Cu(s) + LiNO₃(aq) → ?
Cu: the unreactive tier · Li: the cold-water tier, at the very top

A copper wire stands in lithium nitrate solution. A common first attempt swaps the partners into CuNO₃ + Li. Test it against the series.

Dr. Karmach

Worked example 3: solution

Cu(s) + LiNO₃(aq) → ?
Cu: the unreactive tier · Li: the cold-water tier, at the very top

A common first attempt

Cu + LiNO₃ → CuNO₃ + Li ✗
this asks copper to push its electrons onto Li⁺, three tiers up
Dr. Karmach

Worked example 3: solution

Cu(s) + LiNO₃(aq) → ?
Cu: the unreactive tier · Li: the cold-water tier, at the very top
A common first attempt
Cu + LiNO₃ → CuNO₃ + Li ✗
this asks copper to push its electrons onto Li⁺, three tiers up
Step 2 · Compare positions

Cu sits far below Li. Copper keeps its electrons, and Li⁺ stays dissolved.

Cu(s) + LiNO₃(aq) → no reaction
solid metal below the dissolved cation: no electron hand-off
Dr. Karmach

Worked example 3: solution

Cu(s) + LiNO₃(aq) → ?
Cu: the unreactive tier · Li: the cold-water tier, at the very top
A common first attempt
Cu + LiNO₃ → CuNO₃ + Li ✗
this asks copper to push its electrons onto Li⁺, three tiers up
Step 2 · Compare positions
Cu(s) + LiNO₃(aq) → no reaction
solid metal below the dissolved cation: no electron hand-off
The wire can stand there for years. A swap that looks fine on paper still needs the electron transfer to run downhill in the series.
Dr. Karmach

Worked example 3: the route on the series

Cu(s) + LiNO₃(aq) → no reaction
solid metal: Cu · partner: Li, in the compound · found: no reaction

The arrow points up the series. Copper sits far below lithium, so nothing happens. ✓
Dr. Karmach

Practice 2

Fe(s) + NiSO₄(aq) → FeSO₄(aq) + Ni(s)
observed: an iron nail in nickel(II) sulfate solution darkens with nickel

A classmate reasons that swapping the roles must work as well, and writes Ni + FeSO₄ → NiSO₄ + Fe. Which verdict on that claim is correct?

  1. It stands: every atom count matches, so the reverse runs.
  2. It fails: Ni sits below Fe, so it cannot displace Fe²⁺. Ni + FeSO₄ gives no reaction.
  3. It stands: Ni and Fe both sit above hydrogen, so each can displace the other.
  4. It stands, slowly: the reverse runs, just more slowly, since Ni is the less active metal.
Dr. Karmach

Practice 2: answer B

Ni(s) + FeSO₄(aq) → no reaction (answer B)
Fe: the steam tier · Ni: the acid tier, lower · the solid metal sits below the dissolved cation

A treats balance as permission: Ni 1 = 1, Fe 1 = 1, S 1 = 1, O 4 = 4, yet a balanced equation can describe a reaction that never happens. C compared each metal with hydrogen; the partner here is Fe²⁺, which sits above Ni. D: speed never moves a metal up the series; the ranking decides whether electrons flow at all.

The forward reaction is the evidence: Fe gave its electrons to Ni²⁺. The same ranking forbids Ni from handing them back.
Dr. Karmach

Summary of reaction types

Six reactant patterns cover nearly every product prediction. The solubility rules pick the precipitate; the activity series decides whether displacement runs.

Dr. Karmach

Predicting products in aqueous solutions

HCl(aq) + Na₂CO₃(aq): major species H⁺, Cl⁻, Na⁺, CO₃²⁻
acid + carbonate → salt + CO₂ + H₂O → 2 HCl + Na₂CO₃ → 2 NaCl + CO₂ + H₂O

List the major species actually in the beaker. Match them to a reaction-type pattern; the first match names the products. No match on any pattern means no reaction.

Dr. Karmach

Practice 3: four mixtures

Predict the products, name the pattern, and balance. One of the four gives no reaction.

  1. Al(s) + H₂SO₄(aq)
  2. HF(aq) + KOH(aq)
  3. Ca(OH)₂(aq) + HCl(aq)
  4. HNO₃(aq) + CaCl₂(aq)
Dr. Karmach

Practice 3: solutions

2 Al + 3 H₂SO₄ → Al₂(SO₄)₃ + 3 H₂
metal + acid → salt + H₂, Al above hydrogen · Al: 2 = 2 ✓ · H: 6 = 6 ✓ · S: 3 = 3 ✓ · O: 12 = 12 ✓
HF + KOH → KF + H₂O
acid + hydroxide → salt + water · F: 1 = 1 ✓ · K: 1 = 1 ✓ · O: 1 = 1 ✓ · H: 1 + 1 = 2 ✓
Dr. Karmach

Practice 3: solutions

2 Al + 3 H₂SO₄ → Al₂(SO₄)₃ + 3 H₂
metal + acid → salt + H₂, Al above hydrogen · Al: 2 = 2 ✓ · H: 6 = 6 ✓ · S: 3 = 3 ✓ · O: 12 = 12 ✓
HF + KOH → KF + H₂O
acid + hydroxide → salt + water · F: 1 = 1 ✓ · K: 1 = 1 ✓ · O: 1 = 1 ✓ · H: 1 + 1 = 2 ✓
Ca(OH)₂ + 2 HCl → CaCl₂ + 2 H₂O
acid + hydroxide → salt + water · Ca: 1 = 1 ✓ · Cl: 2 = 2 ✓ · H: 2 + 2 = 4 ✓ · O: 2 = 2 ✓
HNO₃ + CaCl₂ → no reaction
the swap would give HCl + Ca(NO₃)₂: both soluble, both strong · nothing leaves the solution
Three mixtures match a pattern; the fourth matches none. No solid, no gas, no water formed: no reaction is the complete answer.
Dr. Karmach

Check yourself

  1. Aluminum foil sits in copper(II) chloride solution, and aluminum stands above copper in the series. Write the products, balance the equation, and name the element oxidized.
  2. A gold ring survives years of hand washing. Which tier of the series is responsible, and what does that tier say about gold's electrons?

Every equation you can now write, balance, and classify is ready to become arithmetic. The coefficients of a balanced equation are counting ratios: mole ratios, the conversion factors that turn amounts of one substance into amounts of another.

Dr. Karmach

10 · Mole Ratios

Use the coefficients of a balanced equation to convert moles of one substance into moles of any other.

Dr. Karmach

The airbag problem

In a crash, an airbag pellet of sodium azide decomposes into nitrogen gas: 67 liters in 30 milliseconds. Mole ratios determine how much solid to pack.

Dr. Karmach

Why coefficients mean moles

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
2 : 5 : 4 : 2 molecules2 : 5 : 4 : 2 dozen2 : 5 : 4 : 2 mol, the same ratio at every scale

A balanced equation counts molecules. Scaling every amount by the same number keeps the ratio. Avogadro's number is one such multiplier: coefficients count moles too.

Two numbers appear in 2 H₂O. Name each one's job.

2 H₂O
which number may balancing change · which is part of the formula itself
Dr. Karmach

Why coefficients mean moles

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
2 : 5 : 4 : 2 molecules2 : 5 : 4 : 2 dozen2 : 5 : 4 : 2 mol, the same ratio at every scale

A balanced equation counts molecules. Scaling every amount by the same number keeps the ratio. Avogadro's number is one such multiplier: coefficients count moles too.

Two numbers appear in 2 H₂O. Name each one's job.

2 H₂O
which number may balancing change · which is part of the formula itself
2 H₂O
the coefficient 2 may change during balancing ✓ · changing the subscript ₂ would name a different substance ✗
Dr. Karmach

Reading the coefficients

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O

The coefficients count the molecules in the figure. The same numbers apply in moles. Like a recipe, the amounts scale together.

Dr. Karmach

Coefficients become conversion factors

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O

Any two coefficients form a mole ratio: a fraction that converts moles of one substance into moles of another.

4 mol CO₂5 mol O₂ or 5 mol O₂2 mol C₂H₂ or any pair

Write it so the given unit cancels.

Dr. Karmach

The method

The heart of every stoichiometry problem is a mole to mole conversion.

  1. Start from a balanced equation.
  2. Build the ratio wanted over given, so the given unit cancels.
  3. Multiply and cancel; check the result against the coefficients.

Dr. Karmach

Worked example 1

Step 1 · Start from a balanced equation

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂ · wanted: mol CO₂

A welding torch burns 4.5 mol of C₂H₂. How many moles of CO₂ form?

Set it up: which ratio cancels mol C₂H₂?

Dr. Karmach

Worked example 1: solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂

One conversion factor is needed.

Step 2 · Build the ratio, wanted over given

Two orientations exist. Only one cancels the given unit:

4 mol CO₂2 mol C₂H₂ cancels mol C₂H₂ ✓    2 mol C₂H₂4 mol CO₂ cancels nothing ✗
Dr. Karmach

Worked example 1: solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂
Step 2 · Build the ratio, wanted over given
4 mol CO₂2 mol C₂H₂ cancels mol C₂H₂ ✓    2 mol C₂H₂4 mol CO₂ cancels nothing ✗
Step 3 · Multiply and cancel
4.5 mol C₂H₂ × 4 mol CO₂2 mol C₂H₂ = 9.0 mol CO₂
Dr. Karmach

Worked example 1: solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂
Step 2 · Build the ratio, wanted over given
4 mol CO₂2 mol C₂H₂ cancels mol C₂H₂ ✓    2 mol C₂H₂4 mol CO₂ cancels nothing ✗
Step 3 · Multiply and cancel
4.5 mol C₂H₂ × 4 mol CO₂2 mol C₂H₂ = 9.0 mol CO₂
The coefficients make CO₂ double the C₂H₂ (4 vs 2), and 9.0 is double 4.5. ✓
Dr. Karmach

Worked example 1: the route on the map

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂ · found: 9.0 mol CO₂

A is C₂H₂, B is CO₂. One arrow, one conversion factor: the mole ratio. ✓
Dr. Karmach

Your turn: oxygen for the torch

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 3.2 mol C₂H₂ · wanted: mol O₂

The torch consumes O₂ while it burns 3.2 mol of C₂H₂:

3.2 mol C₂H₂ × mol O₂ mol C₂H₂ = mol O₂

Complete the ratio so mol C₂H₂ cancels, then compute.

Dr. Karmach

Your turn: oxygen for the torch

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 3.2 mol C₂H₂ · wanted: mol O₂

The torch consumes O₂ while it burns 3.2 mol of C₂H₂:

3.2 mol C₂H₂ × mol O₂ mol C₂H₂ = mol O₂

Complete the ratio so mol C₂H₂ cancels, then compute.

3.2 mol C₂H₂ × 5 mol O₂2 mol C₂H₂ = 8.0 mol O₂
O₂'s coefficient (5) is larger than C₂H₂'s (2), so the torch needs more O₂ than fuel: 8.0 > 3.2. ✓
Dr. Karmach

Where this goes wrong

N₂ + 3 H₂ → 2 NH₃
Assuming 1:1. "6 mol H₂ → 6 mol NH₃." The equation gives a 2 NH₃ : 3 H₂ ratio, so the answer is 4.0 mol.
Inverting the ratio. (3 mol H₂ / 2 mol NH₃) leaves units of mol H₂²/mol NH₃. Nothing cancels. If the units do not cancel, the fraction is inverted.
Answering with the coefficient. The coefficient (2) is not the answer. It must be applied to the given amount.
Dr. Karmach

Practice 1

2 H₂ + O₂ → 2 H₂O

7.00 mol of O₂ react completely. How many moles of H₂O form?

  1. 7.00
  2. 14.0
  3. 3.50
  4. 2.00
Dr. Karmach

Practice 1: answer B

2 H₂ + O₂ → 2 H₂O
given: 7.00 mol O₂
7.00 mol O₂ × 2 mol H₂O1 mol O₂ = 14.0 mol H₂O (answer B)

A assumed 1:1: 7.00 × 1 = 7.00. C inverted the ratio: 7.00 × (1/2) = 3.50. D answered with the coefficient, 2.

Water's coefficient is double O₂'s, so the answer is double the given. ✓
Dr. Karmach

Practice 2

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂

A blast furnace is fed 4.8 mol CO. How many moles of iron form?

  1. 4.8
  2. 7.2
  3. 3.2
  4. 9.6
Dr. Karmach

Practice 2: answer C

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂
given: 4.8 mol CO
4.8 mol CO × 2 mol Fe3 mol CO = 3.2 mol Fe (answer C)

A assumed 1:1: 4.8 × 1 = 4.8. B inverted the ratio: 4.8 × (3/2) = 7.2. D doubled the given: 4.8 × 2 = 9.6.

Fe's coefficient (2) is smaller than CO's (3), so less Fe forms than CO reacts: 3.2 < 4.8 ✓
Dr. Karmach

Worked example 2: moles of reactant needed

Step 1 · Start from a balanced equation

2 KClO₃ → 2 KCl + 3 O₂
K: 2 = 2 ✓  ·  Cl: 2 = 2 ✓  ·  O: 6 = 6 ✓  ·  given: 7.5 mol O₂ · wanted: mol KClO₃

Heating potassium chlorate releases oxygen gas, one design for emergency oxygen generators. A generator must deliver 7.5 mol of O₂. How many moles of KClO₃ must it hold?

The given sits on the product side. The steps do not change.

Dr. Karmach

Worked example 2: solution

2 KClO₃ → 2 KCl + 3 O₂
given: 7.5 mol O₂ · wanted: mol KClO₃

One conversion factor is needed.

Step 2 · Build the ratio, wanted over given

The ratio, wanted on top: 2 mol KClO₃ over 3 mol O₂, so mol O₂ cancels.

Dr. Karmach

Worked example 2: solution

2 KClO₃ → 2 KCl + 3 O₂
given: 7.5 mol O₂ · wanted: mol KClO₃
Step 2 · Build the ratio, wanted over given Step 3 · Multiply and cancel
7.5 mol O₂ × 2 mol KClO₃3 mol O₂ = 5.0 mol KClO₃
Dr. Karmach

Worked example 2: solution

2 KClO₃ → 2 KCl + 3 O₂
given: 7.5 mol O₂ · wanted: mol KClO₃
Step 2 · Build the ratio, wanted over given Step 3 · Multiply and cancel
7.5 mol O₂ × 2 mol KClO₃3 mol O₂ = 5.0 mol KClO₃
Fewer moles of solid are packed than moles of gas delivered: 2 KClO₃ yield 3 O₂. The ratio converts in either direction across the equation. ✓
Dr. Karmach

Worked example 2: the route on the map

2 KClO₃ → 2 KCl + 3 O₂
given: 7.5 mol O₂ · found: 5.0 mol KClO₃

A is the given, O₂, even though it is a product. B is KClO₃. The route is the same single arrow. ✓
Dr. Karmach

Practice 3

2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O

Greenhouse growers burn butane to enrich the air with CO₂, which speeds plant growth. How many moles of C₄H₁₀ must burn to produce 26.0 mol of CO₂?

  1. 26.0
  2. 52.0
  3. 6.50
  4. 104
Dr. Karmach

Practice 3: answer C

2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
given: 26.0 mol CO₂ · wanted: mol C₄H₁₀
26.0 mol CO₂ × 2 mol C₄H₁₀8 mol CO₂ = 6.50 mol C₄H₁₀ (answer C)

A assumed a 1 : 1 ratio: 26.0 × 1 = 26.0. B multiplied by 2 without dividing by 8: 26.0 × 2 = 52.0. D inverted the ratio: 26.0 × (8/2) = 104.

The ratio 8 : 2 means four CO₂ per butane, so the fuel needed is 26.0 ÷ 4 = 6.50 mol. ✓
Dr. Karmach

Practice 4

C₅H₁₂ + 8 O₂ → 5 CO₂ + 6 H₂O

A refinery flare burns waste pentane. How many moles of gas in total, CO₂ plus H₂O vapor, leave the flare while it consumes 2.40 mol of O₂?

  1. 1.50
  2. 4.80
  3. 7.04
  4. 3.30
Dr. Karmach

Practice 4: answer D

C₅H₁₂ + 8 O₂ → 5 CO₂ + 6 H₂O
given: 2.40 mol O₂ · wanted: total mol CO₂ + H₂O
2.40 mol O₂ × 5 mol CO₂8 mol O₂ = 1.50 mol CO₂ · 2.40 mol O₂ × 6 mol H₂O8 mol O₂ = 1.80 mol H₂O
Dr. Karmach

Practice 4: answer D

C₅H₁₂ + 8 O₂ → 5 CO₂ + 6 H₂O
given: 2.40 mol O₂ · wanted: total mol CO₂ + H₂O
2.40 mol O₂ × 5 mol CO₂8 mol O₂ = 1.50 mol CO₂ · 2.40 mol O₂ × 6 mol H₂O8 mol O₂ = 1.80 mol H₂O
1.50 mol CO₂ + 1.80 mol H₂O = 3.30 mol gas (answer D)

A stopped at the CO₂ alone: 1.50. B assumed 1:1 for each product: 2.40 + 2.40 = 4.80. C inverted both ratios: 2.40 × (8/5) + 2.40 × (8/6) = 3.84 + 3.20 = 7.04.

8 O₂ in, 5 + 6 = 11 gas molecules out: 3.30 > 2.40 ✓
Dr. Karmach

Check yourself

  1. Why does a mole ratio require moles, not grams? (What do coefficients count?)
  2. In N₂ + 3 H₂ → 2 NH₃, which ratio converts mol N₂ → mol NH₃?

A molar-mass conversion on each end of the mole ratio extends this to grams → grams: mass-to-mass stoichiometry. Given two reactants, the same ratios show which one runs out first.

Dr. Karmach

11 · Mass-to-Mass Stoichiometry

Convert a given mass of one substance into the mass or molecule count of another by converting grams to moles, crossing substances with the mole ratio, and converting back.

Dr. Karmach

Heavier than the fuel

One 45-kg tank of gasoline emits about 140 kg of CO₂: triple the fuel's mass. The extra mass comes from oxygen in the air, and stoichiometry predicts it exactly.

Dr. Karmach

Equations count particles, not grams

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
moles = 1 glucose : 6 CO₂  ·  grams = 180.16 : 264.06, not 1 : 6

A balanced equation relates counts (moles), never masses. A mole of glucose weighs four times a mole of CO₂, so a 1:6 mole ratio is not a 1:6 gram ratio.

Dr. Karmach

Convert to moles, then convert back

Convert the given mass to moles, relate moles with the equation, and convert back to mass at the end.

Dr. Karmach

Three conversion factors, one setup

Molar mass converts at each end; the mole ratio is the only factor that switches substances. Chain them so each unit cancels the one before:

g A × 1 mol A(molar mass A) g A × b mol Ba mol A × (molar mass B) g B1 mol B = g B
Dr. Karmach

The method

  1. Grams → moles: convert the given mass with its own molar mass.
  2. Moles → moles: cross substances with the mole ratio. No other step can.
  3. Moles → grams or molecules: convert out with the target's molar mass, or Avogadro's number.
Dr. Karmach

Worked example 1: moles of product from a mass

CH₄ + 2 O₂ → CO₂ + 2 H₂O
given: 8.00 g CH₄ · wanted: mol CO₂

A gas burner consumes 8.00 g of CH₄. How many moles of CO₂ form? (CH₄ 16.04 g/mol, CO₂ 44.01 g/mol)

Write the route first: g CH₄ → mol CH₄ → mol CO₂. Stop at moles.

Dr. Karmach

Worked example 1: solution

CH₄ + 2 O₂ → CO₂ + 2 H₂O
given: 8.00 g CH₄ · wanted: mol CO₂

Two conversion factors are needed.

Step 1 · Grams → moles

CH₄'s own molar mass converts the given mass to moles:

8.00 g CH₄ × 1 mol CH₄16.04 g CH₄ = 0.499 mol CH₄
Dr. Karmach

Worked example 1: solution

CH₄ + 2 O₂ → CO₂ + 2 H₂O
given: 8.00 g CH₄ · wanted: mol CO₂
Step 1 · Grams → moles
8.00 g CH₄ × 1 mol CH₄16.04 g CH₄ = 0.499 mol CH₄
Step 2 · Moles → moles

The mole ratio, written CO₂ over CH₄ (1 : 1), crosses substances:

8.00 g CH₄ × 1 mol CH₄16.04 g CH₄ × 1 mol CO₂1 mol CH₄ = 0.499 mol CO₂
Dr. Karmach

Worked example 1: solution

CH₄ + 2 O₂ → CO₂ + 2 H₂O
given: 8.00 g CH₄ · wanted: mol CO₂
Step 1 · Grams → moles
8.00 g CH₄ × 1 mol CH₄16.04 g CH₄ = 0.499 mol CH₄
Step 2 · Moles → moles
8.00 g CH₄ × 1 mol CH₄16.04 g CH₄ × 1 mol CO₂1 mol CH₄ = 0.499 mol CO₂
A 1 : 1 ratio carries the count across unchanged: 0.499 mol CH₄ makes 0.499 mol CO₂. The question asked for moles, and the chain stops here. ✓
Dr. Karmach

Worked example 1: the route on the map

CH₄ + 2 O₂ → CO₂ + 2 H₂O
given: 8.00 g CH₄ · found: 0.499 mol CO₂

Two arrows: CH₄'s molar mass, then the mole ratio. The route stops at mol B because the question asked for moles. ✓
Dr. Karmach

Worked example 1: one more factor

CH₄ + 2 O₂ → CO₂ + 2 H₂O
found: 0.499 mol CO₂ from 8.00 g CH₄ · wanted: g CO₂ (44.01 g/mol)

Step 3 · Moles → grams

CO₂'s molar mass converts the moles out to mass. The same chain, one factor longer:

8.00 g CH₄ × 1 mol CH₄16.04 g CH₄ × 1 mol CO₂1 mol CH₄ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Dr. Karmach

Worked example 1: one more factor

CH₄ + 2 O₂ → CO₂ + 2 H₂O
found: 0.499 mol CO₂ from 8.00 g CH₄ · wanted: g CO₂ (44.01 g/mol)

Step 3 · Moles → grams

CO₂'s molar mass converts the moles out to mass. The same chain, one factor longer:

8.00 g CH₄ × 1 mol CH₄16.04 g CH₄ × 1 mol CO₂1 mol CH₄ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Grams to grams is not a new method: it is the moles answer with a molar mass on the end. A mole of CO₂ (44.01 g) outweighs a mole of CH₄ (16.04 g), so 8.00 g of fuel becomes 22.0 g of CO₂. ✓
Dr. Karmach

Worked example 1: the grams route on the map

CH₄ + 2 O₂ → CO₂ + 2 H₂O
given: 8.00 g CH₄ · found: 22.0 g CO₂

Three arrows: the moles route plus CO₂'s molar mass at the end. ✓
Dr. Karmach

Worked example 2

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose · wanted: g CO₂

Respiration burns glucose, and the CO₂ is exhaled. What mass of CO₂ forms when 90.0 g of glucose reacts completely? (glucose 180.16 g/mol, CO₂ 44.01 g/mol)

Write the route first: g glucose → mol glucose → mol CO₂ → g CO₂.

Dr. Karmach

Worked example 2: solution

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose

Three conversion factors are needed.

Step 1 · Grams → moles

Glucose's own molar mass converts the given mass to moles. Its unit cancels the given unit:

90.0 g glucose × 1 mol glucose180.16 g glucose
Dr. Karmach

Worked example 2: solution

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose
Step 1 · Grams → moles
90.0 g glucose × 1 mol glucose180.16 g glucose
Step 2 · Moles → moles

The mole ratio is the only factor that crosses substances. Two orientations exist. Only one cancels mol glucose:

6 mol CO₂1 mol glucose cancels mol glucose ✓    1 mol glucose6 mol CO₂ cancels nothing ✗
Dr. Karmach

Worked example 2: solution

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose
Step 1 · Grams → moles
90.0 g glucose × 1 mol glucose180.16 g glucose
Step 2 · Moles → moles Step 3 · Moles → grams

Convert out with the target's molar mass, in one continuous setup. Carry all digits and round once at the end:

90.0 g glucose × 1 mol glucose180.16 g glucose × 6 mol CO₂1 mol glucose × 44.01 g CO₂1 mol CO₂ = 132 g CO₂
Dr. Karmach

Worked example 2: solution

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose
Step 1 · Grams → moles
90.0 g glucose × 1 mol glucose180.16 g glucose
Step 2 · Moles → moles Step 3 · Moles → grams
90.0 g glucose × 1 mol glucose180.16 g glucose × 6 mol CO₂1 mol glucose × 44.01 g CO₂1 mol CO₂ = 132 g CO₂
More mass leaves than entered: the carbon leaves as CO₂, and the added oxygen mass comes from the air. ✓
Dr. Karmach

Worked example 2: the route on the map

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose · found: 132 g CO₂

Three arrows, three conversion factors: glucose's molar mass, the mole ratio, CO₂'s molar mass. ✓
Dr. Karmach

Worked example 3: grams to molecules

2 NaN₃ → 2 Na + 3 N₂
given: 50.0 g NaN₃ · wanted: molecules of N₂

An airbag fills in about 30 milliseconds with N₂ from a pellet of sodium azide. How many molecules of N₂ form when 50.0 g of NaN₃ decomposes? (NaN₃ 65.02 g/mol)

Write the route first: g NaN₃ → mol NaN₃ → mol N₂ → molecules N₂.

Dr. Karmach

Worked example 3: solution

2 NaN₃ → 2 Na + 3 N₂
given: 50.0 g NaN₃ · wanted: molecules of N₂

Three conversion factors are needed.

Step 1 · Grams → moles

NaN₃'s molar mass, 65.02 g per mole, converts 50.0 g to 0.769 mol NaN₃.

Dr. Karmach

Worked example 3: solution

2 NaN₃ → 2 Na + 3 N₂
given: 50.0 g NaN₃ · wanted: molecules of N₂
Step 1 · Grams → moles Step 2 · Moles → moles

The mole ratio, written N₂ over NaN₃ (3 : 2), crosses substances and turns 0.769 mol NaN₃ into 1.1535 mol N₂, unrounded.

Dr. Karmach

Worked example 3: solution

2 NaN₃ → 2 Na + 3 N₂
given: 50.0 g NaN₃ · wanted: molecules of N₂
Step 1 · Grams → moles Step 2 · Moles → moles Step 3 · Moles → molecules

Avogadro's number converts out, with mol N₂ on the bottom so it cancels. Carry all digits and round once at the end:

50.0 g NaN₃ × 1 mol NaN₃65.02 g NaN₃ × 3 mol N₂2 mol NaN₃ × 6.022 × 10²³ molecules N₂1 mol N₂ = 6.95 × 10²³ molecules N₂
Dr. Karmach

Worked example 3: solution

2 NaN₃ → 2 Na + 3 N₂
given: 50.0 g NaN₃ · wanted: molecules of N₂
Step 1 · Grams → moles Step 2 · Moles → moles Step 3 · Moles → molecules
50.0 g NaN₃ × 1 mol NaN₃65.02 g NaN₃ × 3 mol N₂2 mol NaN₃ × 6.022 × 10²³ molecules N₂1 mol N₂ = 6.95 × 10²³ molecules N₂
Coefficients count particles, so the chain can end on a count as easily as on grams. 1.15 mol is a little over one mole, and the count lands a little over 6.022 × 10²³ ✓

Run backward, the chain starts at a count: molecules B → mol B → mol A → g A, with Avogadro's number flipped so molecules cancel.

Dr. Karmach

Worked example 3: the route on the map

2 NaN₃ → 2 Na + 3 N₂
given: 50.0 g NaN₃ · found: 6.95 × 10²³ molecules N₂

Three arrows, three conversion factors: NaN₃'s molar mass, the mole ratio, then Avogadro's number. ✓
Dr. Karmach

Your turn: potassium chlorate

2 KClO₃ → 2 KCl + 3 O₂

Heating potassium chlorate releases oxygen gas. Starting from 61.3 g KClO₃ (122.55 g/mol; O₂ 32.00 g/mol):

61.3 g KClO₃ × 1 mol KClO₃122.55 g KClO₃ × mol O₂ mol KClO₃ × g O₂1 mol O₂ = g O₂

Fill the mole ratio from the coefficients and the last molar mass, then compute.

Dr. Karmach

Your turn: potassium chlorate

2 KClO₃ → 2 KCl + 3 O₂

Heating potassium chlorate releases oxygen gas. Starting from 61.3 g KClO₃ (122.55 g/mol; O₂ 32.00 g/mol):

61.3 g KClO₃ × 1 mol KClO₃122.55 g KClO₃ × mol O₂ mol KClO₃ × g O₂1 mol O₂ = g O₂

Fill the mole ratio from the coefficients and the last molar mass, then compute.

61.3 g KClO₃ × 1 mol KClO₃122.55 g KClO₃ × 3 mol O₂2 mol KClO₃ × 32.00 g O₂1 mol O₂ = 24.0 g O₂
Dr. Karmach

Where this goes wrong

2 KClO₃ → 2 KCl + 3 O₂
given: 61.3 g KClO₃
Applying the mole ratio to grams. 61.3 g × (3/2) = 92.0 g is wrong: coefficients count moles, not grams. Convert first: 61.3 g ÷ 122.55 g/mol = 0.500 mol. The correct answer is 24.0 g.
Skipping the mole ratio. g → mol → g gives 16.0 g. That assumes a 1:1 ratio. The equation gives 2 KClO₃ : 3 O₂, and the mole ratio is the only step that switches substances.
Inverting the ratio. (2 mol KClO₃ / 3 mol O₂) leaves units of mol KClO₃²/mol O₂. Nothing cancels, and 10.7 g is wrong. If the units do not cancel, the fraction is inverted.
Dr. Karmach

Practice 1

C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O

A camping stove burns 25.0 g of propane (44.09 g/mol). What mass of water, in grams, forms? (H₂O 18.02 g/mol)

  1. 10.2
  2. 2.27
  3. 40.9
  4. 2.55
Dr. Karmach

Practice 1: answer C

C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O
given: 25.0 g C₃H₈
25.0 g C₃H₈ × 1 mol C₃H₈44.09 g C₃H₈ × 4 mol H₂O1 mol C₃H₈ × 18.02 g H₂O1 mol H₂O = 40.9 g H₂O (answer C)

A skipped the mole ratio: 25.0/44.09 × 18.02 = 10.2. B stopped at moles: 25.0/44.09 × 4 = 2.27 mol H₂O, one factor short of grams. D inverted the ratio: 25.0/44.09 × (1/4) × 18.02 = 2.55.

The ratio gives four H₂O per C₃H₈, but a mole of H₂O weighs less than half a mole of C₃H₈ (18 vs 44 g). The overall factor is about 1.6: 25.0 → 40.9 ✓
Dr. Karmach

Practice 2

4 Al + 3 O₂ → 2 Al₂O₃

35.0 g of aluminum (26.98 g/mol) oxidizes completely. How many grams of Al₂O₃ (101.96 g/mol) form?

  1. 0.649
  2. 66.1
  3. 132
  4. 265
Dr. Karmach

Practice 2: answer B

4 Al + 3 O₂ → 2 Al₂O₃
given: 35.0 g Al
35.0 g Al × 1 mol Al26.98 g Al × 2 mol Al₂O₃4 mol Al × 101.96 g Al₂O₃1 mol Al₂O₃ = 66.1 g Al₂O₃ (answer B)

A stopped at moles: 35.0/26.98 × (2/4) = 0.649 mol Al₂O₃, one factor short of grams. C skipped the mole ratio: 35.0/26.98 × 101.96 = 132. D inverted the ratio: 35.0/26.98 × (4/2) × 101.96 = 265.

The oxide weighs more than the metal alone. The extra 31.1 g is oxygen from the air. ✓
Dr. Karmach

Practice 3

2 NaHCO₃ → Na₂CO₃ + H₂O + CO₂

Baking soda releases CO₂ as it decomposes in a hot oven. A recipe needs 2.20 g of CO₂ to rise. How many grams of NaHCO₃ (84.01 g/mol) must decompose? (CO₂ 44.01 g/mol)

  1. 4.20
  2. 2.10
  3. 0.100
  4. 8.40
Dr. Karmach

Practice 3: answer D

2 NaHCO₃ → Na₂CO₃ + H₂O + CO₂
given: 2.20 g CO₂ · wanted: g NaHCO₃
2.20 g CO₂ × 1 mol CO₂44.01 g CO₂ × 2 mol NaHCO₃1 mol CO₂ × 84.01 g NaHCO₃1 mol NaHCO₃ = 8.40 g NaHCO₃ (answer D)

A skipped the mole ratio: 2.20/44.01 × 84.01 = 4.20. B inverted the ratio: 2.20/44.01 × (1/2) × 84.01 = 2.10. C stopped at moles: 2.20/44.01 × 2 = 0.100 mol NaHCO₃, one factor short of grams.

The route runs backward just as well: g CO₂ → mol CO₂ → mol NaHCO₃ → g NaHCO₃. Two NaHCO₃ per CO₂, each nearly twice as heavy: about four times the mass, 2.20 → 8.40 ✓
Dr. Karmach

Worked example 4

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si · wanted: g Cr

Silicon extracts chromium metal from its ore. What mass of Cr forms when 42.0 g of Si reacts completely? (Si 28.09 g/mol, Cr 52.00 g/mol)

The equation is already balanced. Read the mole ratio directly from the coefficients.

Dr. Karmach

Worked example 4: solution

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si

Three conversion factors are needed.

Step 1 · Grams → moles

The molar mass, 28.09 g per mole, converts the given mass of Si to moles.

Dr. Karmach

Worked example 4: solution

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si
Step 1 · Grams → moles Step 2 · Moles → moles

The mole ratio, written Cr over Si (4 : 3), crosses substances; mol Si cancels. Only the substances changed; the route is the same.

Dr. Karmach

Worked example 4: solution

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si
Step 1 · Grams → moles Step 2 · Moles → moles Step 3 · Moles → grams

Convert out with Cr's molar mass. The complete chain:

42.0 g Si × 1 mol Si28.09 g Si × 4 mol Cr3 mol Si × 52.00 g Cr1 mol Cr = 104 g Cr

Label every quantity with its substance. A wrong setup shows up as a unit that will not cancel.

Dr. Karmach

Worked example 4: solution

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si
Step 1 · Grams → moles Step 2 · Moles → moles Step 3 · Moles → grams
42.0 g Si × 1 mol Si28.09 g Si × 4 mol Cr3 mol Si × 52.00 g Cr1 mol Cr = 104 g Cr
A mole of Cr (52.00 g) weighs nearly twice a mole of Si (28.09 g), and the ratio gives more moles of Cr (4:3). More mass leaves than entered: 104 > 42.0 ✓
Dr. Karmach

Worked example 4: the route on the map

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si · found: 104 g Cr

The same three arrows as glucose to CO₂. Only the substances changed. ✓
Dr. Karmach

Check yourself

  1. In the g → g route, why must the given mass become moles before the mole ratio is applied? (What do coefficients count?)
  2. Fill in the route: g A → ? → ? → g B. Which of the three factors is the only one that switches substances?

Many problems give two starting masses. Convert each reactant to the same product; whichever gives less product runs out first. That is the limiting reactant.

Dr. Karmach

12 · Limiting Reactant

Decide which reactant runs out first, and compute the product from that reactant alone.

Dr. Karmach

One ingredient runs out first

One bun and one patty per burger. The patties ran out first, so only seven burgers can be made. Reactions work the same way, in moles.

Dr. Karmach

Limiting and excess

2 H₂ + O₂ → 2 H₂O

Reactants are consumed in a fixed ratio, set by the coefficients. The first to run out is the limiting reactant: it stops the reaction and sets the maximum product. What remains of the other is excess.

Dr. Karmach

Count it out

2 H₂ + O₂ → 2 H₂O
start: 6 H₂ and 4 O₂ · each run of the recipe consumes 2 H₂ and 1 O₂, making 2 H₂O

Count the runs: how many H₂O form, and what remains?

Dr. Karmach

Count it out

2 H₂ + O₂ → 2 H₂O
start: 6 H₂ and 4 O₂ · each run of the recipe consumes 2 H₂ and 1 O₂, making 2 H₂O

Count the runs: how many H₂O form, and what remains?

2 H₂ + O₂ → 2 H₂O
run 1: 2 H₂ + 1 O₂ · run 2: 2 H₂ + 1 O₂ · run 3: 2 H₂ + 1 O₂ · no H₂ for a fourthafter: 6 H₂O made · 0 H₂ · 1 O₂ left over

Six H₂O form and one O₂ remains. H₂ started with more molecules and still ran out first.

Dr. Karmach

The test: moles ÷ coefficient

2 H₂ + O₂ → 2 H₂O
H₂: 6.0 ÷ 2 = 3.0 runs · O₂: 4.0 ÷ 1 = 4.0 runs · 3.0 < 4.0, H₂ is spent first

Moles ÷ coefficient counts how many times a reactant can run the recipe. The reactant with the fewest runs is spent first: the division predicts the count-out.

Dr. Karmach

The method

  1. Convert both reactants to moles.
  2. Divide each by its coefficient.
  3. The smaller number limits: that reactant runs out first.
  4. Compute product from the limiting reactant only.
Dr. Karmach

Worked example 1: thermite

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃

Rail-welding thermite: 4.6 mol Al mixed with 3.8 mol Fe₂O₃. How many moles of Al₂O₃ can form?

Divide each reactant's moles by its coefficient. The smaller result marks the limiting reactant.

Dr. Karmach

Worked example 1: which reactant limits

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃

Step 1 · Convert both reactants to moles

Both amounts are already in moles, so Step 1 is complete.

Step 2 · Divide each by its coefficient

Al: 4.6 mol2 = 2.3
Dr. Karmach

Worked example 1: which reactant limits

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃
Step 1 · Convert both reactants to moles Step 2 · Divide each by its coefficient
Al: 4.6 mol2 = 2.3
Fe₂O₃: the same division.
Fe₂O₃: 3.8 mol1 = 3.8
Dr. Karmach

Worked example 1: which reactant limits

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃
Step 1 · Convert both reactants to moles Step 2 · Divide each by its coefficient
Al: 4.6 mol2 = 2.3
Fe₂O₃: 3.8 mol1 = 3.8
Step 3 · The smaller number limits
2.3 < 3.8, so Al limits. Fe₂O₃ is excess.
Dr. Karmach

Worked example 1: how much product

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al limits

Step 4 · Compute product from the limiting reactant only

4.6 mol Al × 1 mol Al₂O₃2 mol Al = 2.3 mol Al₂O₃
Dr. Karmach

Worked example 1: how much product

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al limits

Step 4 · Compute product from the limiting reactant only

4.6 mol Al × 1 mol Al₂O₃2 mol Al = 2.3 mol Al₂O₃
Fe₂O₃ alone could give 3.8 mol, but the reaction stops when Al runs out, at 2.3 mol. The smaller result is the amount that can actually form. ✓
Dr. Karmach

Worked example 1: the route on the map

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · found: 2.3 mol Al₂O₃

Both amounts started in moles, so Step 1 used no arrow. Steps 2 and 3 happen off the map. In Step 4 only Al, the limiting reactant, crosses the bridge: A is Al, B is Al₂O₃. ✓
Dr. Karmach

Worked example 2: full mass chain

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂

An ammonia reactor is charged with 42.0 g N₂ and 12.0 g H₂. What mass of NH₃ can form?

A common first attempt: H₂ has the smaller mass, 12.0 g, so H₂ limits. Test it.

Dr. Karmach

Worked example 2: which reactant limits

N₂ + 3 H₂ → 2 NH₃ · given: 42.0 g N₂ and 12.0 g H₂

Four conversion factors are needed: one molar mass for each reactant, then the mole ratio, then the target's molar mass.

Step 1 · Convert both reactants to moles

42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Dr. Karmach

Worked example 2: which reactant limits

N₂ + 3 H₂ → 2 NH₃ · given: 42.0 g N₂ and 12.0 g H₂
Step 1 · Convert both reactants to moles
42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Step 2 · Divide each by its coefficient
N₂: 1.50 mol1 = 1.50 · H₂: 5.95 mol3 = 1.98
Dr. Karmach

Worked example 2: which reactant limits

N₂ + 3 H₂ → 2 NH₃ · given: 42.0 g N₂ and 12.0 g H₂
Step 1 · Convert both reactants to moles
42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Step 2 · Divide each by its coefficient
N₂: 1.50 mol1 = 1.50 · H₂: 5.95 mol3 = 1.98
Step 3 · The smaller number limits
1.50 < 1.98, so N₂ limits. H₂ is excess.
Dr. Karmach

Worked example 2: how much product

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ · N₂ limits, 1.50 mol

Step 4 · Compute product from the limiting reactant only

1.50 mol N₂ × 2 mol NH₃1 mol N₂ × 17.03 g NH₃1 mol NH₃ = 51.1 g NH₃
Dr. Karmach

Worked example 2: how much product

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ · N₂ limits, 1.50 mol

Step 4 · Compute product from the limiting reactant only

1.50 mol N₂ × 2 mol NH₃1 mol N₂ × 17.03 g NH₃1 mol NH₃ = 51.1 g NH₃
The smaller mass, 12.0 g of H₂, is the excess; the larger mass, 42.0 g of N₂, runs out first. Mass does not identify the limiting reactant. ✓
Dr. Karmach

Worked example 2: the route on the map

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ · found: 51.1 g NH₃

Step 1 runs arrow 1 twice (N₂, then H₂). Steps 2 and 3 happen off the map. In Step 4 only N₂, the limiting reactant, rides on to grams of NH₃. ✓
Dr. Karmach

A second path: compare the product

  1. Grams to moles, for each reactant.
  2. Mole ratio to moles of product.
  3. Moles to grams of product.
  4. The reactant that makes less product limits. That amount is the theoretical yield.
Dr. Karmach

Worked example 3: the product path

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂

The same ammonia charge, solved a second way.

Convert each reactant to grams of NH₃ and compare the two results.

Dr. Karmach

Worked example 3: the NH₃ each reactant can make

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂

Three conversion factors per reactant: its molar mass, the mole ratio, and the molar mass of NH₃.

Step 1 · Grams to moles, for each reactant

42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Dr. Karmach

Worked example 3: the NH₃ each reactant can make

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂
Step 1 · Grams to moles, for each reactant
42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Step 2 · Mole ratio to moles of product
1.50 mol N₂ × 2 mol NH₃1 mol N₂ = 3.00 mol NH₃ · 5.95 mol H₂ × 2 mol NH₃3 mol H₂ = 3.97 mol NH₃
Dr. Karmach

Worked example 3: the NH₃ each reactant can make

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂
Step 1 · Grams to moles, for each reactant
42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Step 2 · Mole ratio to moles of product
1.50 mol N₂ × 2 mol NH₃1 mol N₂ = 3.00 mol NH₃ · 5.95 mol H₂ × 2 mol NH₃3 mol H₂ = 3.97 mol NH₃
Each reactant now has its own amount of NH₃: 3.00 mol from N₂, 3.97 mol from H₂.
Dr. Karmach

Worked example 3: grams of NH₃, then compare

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ · N₂ → 3.00 mol NH₃ · H₂ → 3.97 mol NH₃

Step 3 · Moles to grams of product

3.00 mol NH₃ × 17.03 g NH₃1 mol NH₃ = 51.1 g NH₃ from N₂
3.97 mol NH₃ × 17.03 g NH₃1 mol NH₃ = 67.6 g NH₃ from H₂
Dr. Karmach

Worked example 3: grams of NH₃, then compare

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ · N₂ → 3.00 mol NH₃ · H₂ → 3.97 mol NH₃

Step 3 · Moles to grams of product

3.00 mol NH₃ × 17.03 g NH₃1 mol NH₃ = 51.1 g NH₃ from N₂
3.97 mol NH₃ × 17.03 g NH₃1 mol NH₃ = 67.6 g NH₃ from H₂
Step 4 · The reactant that makes less product limits
51.1 g < 67.6 g, so N₂ limits. The theoretical yield is 51.1 g NH₃; the 67.6 g from H₂ can never form ✓
Dr. Karmach

Worked example 3: the route on the map

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ · found: 51.1 g NH₃ from N₂, 67.6 g from H₂

The same three arrows, run once per reactant: A = N₂, then A = H₂; B = NH₃. The smaller grams of B names the limiting reactant. ✓
Dr. Karmach

Worked example 3: both paths agree

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ → 1.50 mol · 12.0 g H₂ → 5.95 mol
moles ÷ coefficient product path
N₂ 1.50 ÷ 1 = 1.50 1.50 × 2/1 = 3.00 mol NH₃ → 51.1 g
H₂ 5.95 ÷ 3 = 1.98 5.95 × 2/3 = 3.97 mol NH₃ → 67.6 g
verdict N₂ limits N₂ limits, 51.1 g NH₃
Dr. Karmach

Worked example 3: both paths agree

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ → 1.50 mol · 12.0 g H₂ → 5.95 mol
moles ÷ coefficient product path
N₂ 1.50 ÷ 1 = 1.50 1.50 × 2/1 = 3.00 mol NH₃ → 51.1 g
H₂ 5.95 ÷ 3 = 1.98 5.95 × 2/3 = 3.97 mol NH₃ → 67.6 g
verdict N₂ limits N₂ limits, 51.1 g NH₃
Each product amount is the division result × 2, the coefficient of NH₃ (N₂: 1.50 × 2 = 3.00 mol). Multiplying both by the same number keeps the smaller one smaller, so both paths always name the same limiting reactant ✓
Dr. Karmach

Your turn: finish the comparison

2 Mg + O₂ → 2 MgO

A signal flare holds 0.80 mol Mg and 0.50 mol O₂. How many moles of MgO form?

Mg: 0.80 mol2 = 0.40 · O₂: 0.50 mol1 =

Limiting reactant:

Dr. Karmach

Your turn: finish the comparison

2 Mg + O₂ → 2 MgO

A signal flare holds 0.80 mol Mg and 0.50 mol O₂. How many moles of MgO form?

Mg: 0.80 mol2 = 0.40 · O₂: 0.50 mol1 =

Limiting reactant:

O₂: 0.50 / 1 = 0.50 · Mg: 0.40 is smaller, so Mg limits · 0.80 mol Mg × 2 mol MgO2 mol Mg = 0.80 mol MgO
Dr. Karmach

Worked example 4: how much excess remains

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al: 4.6 ÷ 2 = 2.3 · Fe₂O₃: 3.8 ÷ 1 = 3.8 · Al limits

A thermite mix holds 4.6 mol Al and 3.8 mol Fe₂O₃; Al limits. How many moles of Fe₂O₃ remain when the reaction stops?

Convert the limiting reactant's amount to the Fe₂O₃ it consumes, then subtract from the amount loaded.

Dr. Karmach

Worked example 4: solution

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al limits

Consumed by the limiting reactant

The mole ratio converts the Al that reacts into the Fe₂O₃ it consumes:

4.6 mol Al × 1 mol Fe₂O₃2 mol Al = 2.3 mol Fe₂O₃ consumed
Dr. Karmach

Worked example 4: solution

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al limits

Consumed by the limiting reactant

The mole ratio converts the Al that reacts into the Fe₂O₃ it consumes:

4.6 mol Al × 1 mol Fe₂O₃2 mol Al = 2.3 mol Fe₂O₃ consumed
Left over
3.8 mol loaded − 2.3 mol consumed = 1.5 mol Fe₂O₃ left over
Dr. Karmach

Worked example 4: solution

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al limits

Consumed by the limiting reactant

The mole ratio converts the Al that reacts into the Fe₂O₃ it consumes:

4.6 mol Al × 1 mol Fe₂O₃2 mol Al = 2.3 mol Fe₂O₃ consumed
Left over
3.8 mol loaded − 2.3 mol consumed = 1.5 mol Fe₂O₃ left over
The leftover lands between zero and the 3.8 mol loaded: what Al could not consume. ✓
Dr. Karmach

Worked example 4: the route on the map

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al limits · found: 1.5 mol Fe₂O₃ left over

A is Al, B is Fe₂O₃: one mole ratio gives the 2.3 mol consumed. The subtraction from the 3.8 mol loaded happens off the map. ✓
Dr. Karmach

Where this goes wrong

Picking the limiting reactant by mass. In N₂ + 3 H₂ → 2 NH₃, the smaller mass, 12.0 g of H₂ against 42.0 g of N₂, is the excess. Mass does not identify the limiting reactant; moles ÷ coefficient does.
Comparing raw moles. In 2 Mg + O₂ → 2 MgO, 0.50 mol O₂ is fewer moles than 0.80 mol Mg. But two Mg are consumed per O₂: 0.40 vs 0.50, so Mg limits and 0.80 mol MgO forms.
2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃
Building product from the excess reactant. With 4.6 mol Al and 3.8 mol Fe₂O₃, the 3.8 mol suggests 3.8 mol Al₂O₃. The reaction stops at 2.3 mol, when Al runs out. Compute product from the limiting reactant only.
Applying the mole ratio to grams. Coefficients count moles, not grams. Convert each mass to moles before comparing.
Dr. Karmach

Practice 1

2 Al + 3 Cl₂ → 2 AlCl₃

10.0 g of Al foil reacts with 30.0 g of Cl₂ gas. What is the maximum mass of AlCl₃, in grams? (Al 26.98 g/mol · Cl₂ 70.90 g/mol · AlCl₃ 133.33 g/mol)

  1. 37.6
  2. 0.282
  3. 56.4
  4. 84.6
Dr. Karmach

Practice 1: answer A

2 Al + 3 Cl₂ → 2 AlCl₃
given: 10.0 g Al, 30.0 g Cl₂ · Al: 0.371 ÷ 2 = 0.185, excess · Cl₂: 0.423 ÷ 3 = 0.141 ← limits
30.0 g Cl₂ × 1 mol Cl₂70.90 g Cl₂ × 2 mol AlCl₃3 mol Cl₂ × 133.33 g AlCl₃1 mol AlCl₃ = 37.6 g AlCl₃ (answer A)

B stopped at moles: 30.0/70.90 × (2/3) = 0.282 mol AlCl₃, one factor short of grams. C skipped the mole ratio: 30.0/70.90 × 133.33 = 56.4. D inverted the ratio: 30.0/70.90 × (3/2) × 133.33 = 84.6.

Cl₂ brings three times the grams of Al, yet it runs out first: three Cl₂ at 70.90 g each are consumed per two Al ✓
Dr. Karmach

Practice 2

CO + 2 H₂ → CH₃OH

A methanol reactor is fed 14.0 g of CO and 3.00 g of H₂. What is the maximum mass of CH₃OH, in grams? (CO 28.01 g/mol · H₂ 2.016 g/mol · CH₃OH 32.04 g/mol)

  1. 23.8
  2. 16.0
  3. 449
  4. 0.500
Dr. Karmach

Practice 2: answer B

CO + 2 H₂ → CH₃OH
given: 14.0 g CO and 3.00 g H₂ · CO: 0.500 ÷ 1 = 0.500 ← limits · H₂: 1.49 ÷ 2 = 0.744, excess
14.0 g CO × 1 mol CO28.01 g CO × 1 mol CH₃OH1 mol CO × 32.04 g CH₃OH1 mol CH₃OH = 16.0 g CH₃OH (answer B)

A took the smaller mass, H₂, as limiting: 3.00/2.016 × (1/2) × 32.04 = 23.8. C skipped the grams-to-moles step and treated grams of CO as moles: 14.0 × 32.04 = 449. D stopped at moles: 14.0/28.01 × (1/1) = 0.500 mol CH₃OH, one factor short of grams.

Mass balance: 0.98 g H₂ is left over, and 16.0 + 0.98 = 17.0 g loaded ✓
Dr. Karmach

Practice 3: the product path

2 NaOH + CO₂ → Na₂CO₃ + H₂O

A CO₂ scrubber cartridge holds 36.0 g of NaOH and takes in 22.0 g of CO₂. What is the theoretical yield of Na₂CO₃, in grams? (NaOH 40.00 g/mol · CO₂ 44.01 g/mol · Na₂CO₃ 105.99 g/mol)

  1. 53.0
  2. 0.450
  3. 47.7
  4. 191
  5. 95.4
Dr. Karmach

Practice 3: answer C

2 NaOH + CO₂ → Na₂CO₃ + H₂O
given: 36.0 g NaOH → 0.900 mol · 22.0 g CO₂ → 0.500 mol
0.900 mol NaOH × 1 mol Na₂CO₃2 mol NaOH × 105.99 g Na₂CO₃1 mol Na₂CO₃ = 47.7 g Na₂CO₃ from NaOH
0.500 mol CO₂ × 1 mol Na₂CO₃1 mol CO₂ × 105.99 g Na₂CO₃1 mol Na₂CO₃ = 53.0 g Na₂CO₃ from CO₂
Dr. Karmach

Practice 3: answer C

2 NaOH + CO₂ → Na₂CO₃ + H₂O
given: 36.0 g NaOH → 0.900 mol · 22.0 g CO₂ → 0.500 mol
0.900 mol NaOH × 1 mol Na₂CO₃2 mol NaOH × 105.99 g Na₂CO₃1 mol Na₂CO₃ = 47.7 g Na₂CO₃ from NaOH
0.500 mol CO₂ × 1 mol Na₂CO₃1 mol CO₂ × 105.99 g Na₂CO₃1 mol Na₂CO₃ = 53.0 g Na₂CO₃ from CO₂
47.7 g < 53.0 g, so NaOH limits: theoretical yield 47.7 g Na₂CO₃ (answer C) ✓

A kept the larger amount, from CO₂, the excess (also the smaller mass and fewer moles): 53.0. B stopped at moles: 0.900 × (1/2) = 0.450. D inverted the ratio: 0.900 × 2 × 105.99 = 191. E skipped the ratio: 0.900 × 105.99 = 95.4.

Dr. Karmach

Practice 4

P₄ + 6 Cl₂ → 4 PCl₃

A flask holds 0.50 mol P₄ and 2.4 mol Cl₂. How many moles of PCl₃ can form?

  1. 1.6
  2. 2.0
  3. 2.4
  4. 3.6
Dr. Karmach

Practice 4: answer A

P₄ + 6 Cl₂ → 4 PCl₃
given: 0.50 mol P₄ and 2.4 mol Cl₂
P₄: 0.50 mol1 = 0.50 (excess) · Cl₂: 2.4 mol6 = 0.40 ← Cl₂ limits
2.4 mol Cl₂ × 4 mol PCl₃6 mol Cl₂ = 1.6 mol PCl₃ (answer A)

B compared raw moles, called P₄ limiting, and built product from it: 0.50 × (4/1) = 2.0. C carried the 2.4 mol of Cl₂ across as 1:1: 2.4 × 1 = 2.4. D inverted the ratio: 2.4 × (6/4) = 3.6.

Cl₂ has nearly five times the moles of P₄ (2.4 vs 0.50), yet it runs out first: six are consumed per P₄ ✓
Dr. Karmach

Practice 5

TiCl₄ + 2 Mg → Ti + 2 MgCl₂

A titanium reactor is charged with 50.00 g of TiCl₄ and 20.00 g of Mg. What mass of the excess reactant, in grams, is left over when the reaction stops? (TiCl₄ 189.67 g/mol · Mg 24.31 g/mol)

  1. 12.82
  2. 16.80
  3. 13.59
  4. 7.18
Dr. Karmach

Practice 5: answer D

TiCl₄ + 2 Mg → Ti + 2 MgCl₂
given: 50.00 g TiCl₄ and 20.00 g Mg · TiCl₄: 0.2636 ÷ 1 = 0.2636 ← limits · Mg: 0.8227 ÷ 2 = 0.4114, excess
50.00 g TiCl₄ × 1 mol TiCl₄189.67 g TiCl₄ × 2 mol Mg1 mol TiCl₄ × 24.31 g Mg1 mol Mg = 12.82 g Mg consumed
Dr. Karmach

Practice 5: answer D

TiCl₄ + 2 Mg → Ti + 2 MgCl₂
given: 50.00 g TiCl₄ and 20.00 g Mg · TiCl₄: 0.2636 ÷ 1 = 0.2636 ← limits · Mg: 0.8227 ÷ 2 = 0.4114, excess
50.00 g TiCl₄ × 1 mol TiCl₄189.67 g TiCl₄ × 2 mol Mg1 mol TiCl₄ × 24.31 g Mg1 mol Mg = 12.82 g Mg consumed
20.00 g loaded − 12.82 g consumed = 7.18 g Mg left over (answer D)

A stopped at the Mg consumed, 12.82 g. B inverted the ratio: 20.00 − 50.00/189.67 × (1/2) × 24.31 = 16.80. C skipped it: 20.00 − 50.00/189.67 × 24.31 = 13.59.

The smaller mass, Mg, is the excess. The leftover lies between zero and the 20.00 g loaded ✓
Dr. Karmach

Check yourself

  1. Two reactant masses are given. List the steps of both paths that identify the limiting reactant. (Where do the coefficients enter each one?)
  2. Why does neither the smallest mass nor the fewest moles identify the limiting reactant?

The product the limiting reactant allows is the theoretical yield: the maximum the reaction can produce. Percent yield compares the amount actually collected to that maximum: actual over theoretical, × 100.

Dr. Karmach

13 · Percent Yield

Compare the mass a reaction actually delivers to the maximum stoichiometry allows, and report it as a percent yield.

Dr. Karmach

Three cookies short

A cookie recipe promises two dozen. The tray comes out with 21: batter stuck to the bowl, one burned. Chemical reactions come up short the same way.

Dr. Karmach

Theoretical yield: the maximum stoichiometry allows

2 Mg + O₂ → 2 MgO
given: 10.0 g Mg · the chain g Mg → mol Mg → mol MgO → g MgO allows at most 16.6 g

Mass-to-mass stoichiometry computes the most product the given amounts can form: the theoretical yield. A real experiment collects less. Percent yield reports how much of that maximum was actually delivered.

Dr. Karmach

Actual yield is measured on the balance

2 Mg + O₂ → 2 MgO
theoretical: 16.6 g MgO (computed) · actual: 14.1 g MgO (weighed)

The actual yield is the mass of product collected, read off the balance after the experiment. A problem either states it or gives a typical percent yield that predicts it.

Dr. Karmach

Where the missing mass goes

Side reactions consume reactant without making the product. Some reactant never reacts. Some product stays behind in transfer: on the filter, in the crucible. Every loss lowers the actual yield.

Dr. Karmach

Percent yield

percent yield = actual yield ÷ theoretical yield × 100
actual = weighed · theoretical = computed · same substance, same unit
actual yield = percent yield ÷ 100 × theoretical yield
the same equation solved for actual · a known typical yield predicts what a run delivers

Both masses refer to the product. The fraction compares the collected mass to the maximum; × 100 states it as a percent. A real preparation lands below 100%.

Dr. Karmach

The method

  1. Compute the theoretical yield: the maximum product mass. Two reactant amounts given: work from the limiting reactant.
  2. Take the actual yield from the problem: stated, or the unknown.
  3. Divide: actual ÷ theoretical × 100.
actual yield = percent yield ÷ 100 × theoretical yield
percent given, actual wanted: step 3 solved for actual
Dr. Karmach

Worked example 1: heating limestone

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂ collected · wanted: percent yield

A kiln charge of 50.0 g CaCO₃ is heated until no more gas comes off. The CO₂ collected weighs 18.5 g. What is the percent yield? (CaCO₃ 100.09 g/mol · CO₂ 44.01 g/mol)

A common first attempt: 18.5 ÷ 50.0 × 100 = 37.0%. Test it.

Dr. Karmach

Worked example 1: solution

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂

Three conversion factors build the theoretical yield.

Step 1 · Compute the theoretical yield

50.0 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol CO₂1 mol CaCO₃ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Dr. Karmach

Worked example 1: solution

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂
Step 1 · Compute the theoretical yield
50.0 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol CO₂1 mol CaCO₃ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Step 2 · Take the actual yield from the problem

The balance reads 18.5 g. The first attempt divided by 50.0 g of CaCO₃, a different substance. The 100% mark is 22.0 g: the most CO₂ this charge can form.

Dr. Karmach

Worked example 1: solution

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂
Step 1 · Compute the theoretical yield
50.0 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol CO₂1 mol CaCO₃ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Step 2 · Take the actual yield from the problem Step 3 · Divide: actual ÷ theoretical × 100
18.5 g CO₂22.0 g CO₂ × 100 = 84.1%
Dr. Karmach

Worked example 1: solution

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂
Step 1 · Compute the theoretical yield
50.0 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol CO₂1 mol CaCO₃ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Step 2 · Take the actual yield from the problem Step 3 · Divide: actual ÷ theoretical × 100
18.5 g CO₂22.0 g CO₂ × 100 = 84.1%
Below 100% ✓. Of every 100 g of CO₂ the equation allows, the kiln delivered 84. The 37.0% first attempt compared product to reactant, not product to product.
Dr. Karmach

Worked example 2: two reactant amounts

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · actual: 14.2 g PbI₂ · wanted: percent yield

Two clear solutions are mixed and bright yellow PbI₂ precipitates. The dried solid weighs 14.2 g. What is the percent yield? (Pb(NO₃)₂ 331.2 g/mol · KI 166.00 g/mol · PbI₂ 461.0 g/mol)

Amounts of both reactants are given. The theoretical yield comes from the limiting reactant.

Dr. Karmach

Worked example 2: which reactant limits

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · actual: 14.2 g PbI₂

Four conversion factors are needed: one molar mass for each reactant, then the mole ratio and the product's molar mass.

Step 1 · Compute the theoretical yield

15.0 g Pb(NO₃)₂ × 1 mol Pb(NO₃)₂331.2 g Pb(NO₃)₂ = 0.0453 mol · 12.0 g KI × 1 mol KI166.00 g KI = 0.0723 mol
Dr. Karmach

Worked example 2: which reactant limits

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · actual: 14.2 g PbI₂
Step 1 · Compute the theoretical yield
15.0 g Pb(NO₃)₂ × 1 mol Pb(NO₃)₂331.2 g Pb(NO₃)₂ = 0.0453 mol · 12.0 g KI × 1 mol KI166.00 g KI = 0.0723 mol
Moles ÷ coefficient: the smaller result marks the limiting reactant.
Pb(NO₃)₂: 0.0453 mol1 = 0.0453 (excess) · KI: 0.0723 mol2 = 0.0362 ← smaller: KI limits
Dr. Karmach

Worked example 2: which reactant limits

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · actual: 14.2 g PbI₂
Step 1 · Compute the theoretical yield
15.0 g Pb(NO₃)₂ × 1 mol Pb(NO₃)₂331.2 g Pb(NO₃)₂ = 0.0453 mol · 12.0 g KI × 1 mol KI166.00 g KI = 0.0723 mol
Pb(NO₃)₂: 0.0453 mol1 = 0.0453 (excess) · KI: 0.0723 mol2 = 0.0362 ← smaller: KI limits
0.0362 < 0.0453: KI runs out first. The theoretical yield comes from KI alone.
Dr. Karmach

Worked example 2: the percent yield

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · KI limits, 0.0723 mol · actual: 14.2 g PbI₂

Step 1 · Compute the theoretical yield

12.0 g KI × 1 mol KI166.00 g KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 16.66 g PbI₂ theoretical
Dr. Karmach

Worked example 2: the percent yield

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · KI limits, 0.0723 mol · actual: 14.2 g PbI₂

Step 1 · Compute the theoretical yield

12.0 g KI × 1 mol KI166.00 g KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 16.66 g PbI₂ theoretical
Step 2 · Take the actual yield from the problem

The dried precipitate weighs 14.2 g. Measured on the balance, not computed.

Dr. Karmach

Worked example 2: the percent yield

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · KI limits, 0.0723 mol · actual: 14.2 g PbI₂

Step 1 · Compute the theoretical yield

12.0 g KI × 1 mol KI166.00 g KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 16.66 g PbI₂ theoretical
Step 2 · Take the actual yield from the problem Step 3 · Divide: actual ÷ theoretical × 100
14.2 g PbI₂16.66 g PbI₂ × 100 = 85.2%
Dr. Karmach

Worked example 2: the percent yield

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · KI limits, 0.0723 mol · actual: 14.2 g PbI₂

Step 1 · Compute the theoretical yield

12.0 g KI × 1 mol KI166.00 g KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 16.66 g PbI₂ theoretical
Step 2 · Take the actual yield from the problem Step 3 · Divide: actual ÷ theoretical × 100
14.2 g PbI₂16.66 g PbI₂ × 100 = 85.2%
Below 100% ✓. Some PbI₂ stayed dissolved and some clung to the filter: the balance reads less than the maximum.
Dr. Karmach

Your turn: blast furnace iron

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂
given: 80.0 g Fe₂O₃, CO in excess · actual: 47.6 g Fe

A furnace run converts 80.0 g Fe₂O₃ to iron with excess CO and taps 47.6 g of Fe. (Fe₂O₃ 159.70 g/mol · Fe 55.85 g/mol)

80.0 g Fe₂O₃ × 1 mol Fe₂O₃159.70 g Fe₂O₃ × mol Fe mol Fe₂O₃ × 55.85 g Fe1 mol Fe = g Fe
percent yield: 47.6 g Fe g Fe × 100 =

Fill the mole ratio, the theoretical yield, then the percent.

Dr. Karmach

Your turn: blast furnace iron

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂
given: 80.0 g Fe₂O₃, CO in excess · actual: 47.6 g Fe
80.0 g Fe₂O₃ × 1 mol Fe₂O₃159.70 g Fe₂O₃ × mol Fe mol Fe₂O₃ × 55.85 g Fe1 mol Fe = g Fe
percent yield: 47.6 g Fe g Fe × 100 =
ratio: 2 mol Fe1 mol Fe₂O₃ · theoretical: 55.95 g Fe · 47.6 g Fe55.95 g Fe × 100 = 85.1%
Dr. Karmach

Where this goes wrong

Swapping actual and theoretical. With 14.2 g of PbI₂ collected and 16.66 g possible, 16.66 ÷ 14.2 × 100 = 117%. No experiment beats its maximum; a percent above 100 means the ratio is upside down. Actual goes on top: 14.2 ÷ 16.66 × 100 = 85.2%.
Computing the theoretical yield from the excess reactant. In Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃, with 15.0 g Pb(NO₃)₂ and 12.0 g KI, the Pb(NO₃)₂ chain gives 20.88 g and 14.2 ÷ 20.88 × 100 = 68.0%. KI runs out first: the maximum is 16.66 g and the yield is 85.2%.
Comparing product to starting material. In Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂, 47.6 g of Fe from 80.0 g of Fe₂O₃ suggests 47.6 ÷ 80.0 × 100 = 59.5%. The 100% mark is the 55.95 g of Fe stoichiometry allows, and the yield is 85.1%.
Reporting the fraction as the percent. 18.5 ÷ 22.0 = 0.841 is a fraction of the maximum. Multiplied by 100 it becomes the percent yield, 84.1%. An answer of 0.841% would mean nearly everything was lost.
Dr. Karmach

Practice 1

2 H₂O₂ → 2 H₂O + O₂

A bottle of hydrogen peroxide decomposes completely. From 40.0 g of H₂O₂, 15.6 g of O₂ is collected. What is the percent yield? (H₂O₂ 34.02 g/mol · O₂ 32.00 g/mol)

  1. 121
  2. 82.9
  3. 0.829
  4. 41.5
Dr. Karmach

Practice 1: answer B

2 H₂O₂ → 2 H₂O + O₂
given: 40.0 g H₂O₂ · actual: 15.6 g O₂
40.0 g H₂O₂ × 1 mol H₂O₂34.02 g H₂O₂ × 1 mol O₂2 mol H₂O₂ × 32.00 g O₂1 mol O₂ = 18.81 g O₂ theoretical
15.6 g O₂18.81 g O₂ × 100 = 82.9% (answer B)

A flipped the fraction, theoretical over actual: 18.81/15.6 × 100 = 121%, more product than the reaction can make. C left the fraction as a decimal: 15.6/18.81 = 0.829, and the × 100 makes it 82.9%. D skipped the mole ratio in the theoretical yield: 40.0/34.02 × 32.00 = 37.6 g, then 15.6/37.6 × 100 = 41.5%.

Dr. Karmach

Practice 1: answer B

2 H₂O₂ → 2 H₂O + O₂
given: 40.0 g H₂O₂ · actual: 15.6 g O₂
40.0 g H₂O₂ × 1 mol H₂O₂34.02 g H₂O₂ × 1 mol O₂2 mol H₂O₂ × 32.00 g O₂1 mol O₂ = 18.81 g O₂ theoretical
15.6 g O₂18.81 g O₂ × 100 = 82.9% (answer B)
The product is a gas, and some escapes collection. About 83 g reached the flask for every 100 g possible. Below 100% ✓
Dr. Karmach

Practice 2

C₇H₆O₃ + C₄H₆O₃ → C₉H₈O₄ + C₂H₄O₂
salicylic acid + acetic anhydride → aspirin + acetic acid

A student mixes 2.00 g of salicylic acid with 5.00 g of acetic anhydride and collects 2.15 g of aspirin. What is the percent yield? (C₇H₆O₃ 138.12 g/mol · C₄H₆O₃ 102.09 g/mol · C₉H₈O₄ 180.16 g/mol)

  1. 24.4
  2. 121
  3. 0.824
  4. 82.4
Dr. Karmach

Practice 2: answer D

C₇H₆O₃ + C₄H₆O₃ → C₉H₈O₄ + C₂H₄O₂
given: 2.00 g C₇H₆O₃ and 5.00 g C₄H₆O₃ · actual: 2.15 g C₉H₈O₄ · C₇H₆O₃: 0.01448 ÷ 1 ← limits · C₄H₆O₃: 0.04898 ÷ 1, excess
2.00 g C₇H₆O₃ × 1 mol C₇H₆O₃138.12 g C₇H₆O₃ × 1 mol C₉H₈O₄1 mol C₇H₆O₃ × 180.16 g C₉H₈O₄1 mol C₉H₈O₄ = 2.61 g theoretical
2.15 g C₉H₈O₄2.61 g C₉H₈O₄ × 100 = 82.4% (answer D)
Dr. Karmach

Practice 2: answer D

C₇H₆O₃ + C₄H₆O₃ → C₉H₈O₄ + C₂H₄O₂
given: 2.00 g C₇H₆O₃ and 5.00 g C₄H₆O₃ · actual: 2.15 g C₉H₈O₄ · C₇H₆O₃: 0.01448 ÷ 1 ← limits · C₄H₆O₃: 0.04898 ÷ 1, excess
2.00 g C₇H₆O₃ × 1 mol C₇H₆O₃138.12 g C₇H₆O₃ × 1 mol C₉H₈O₄1 mol C₇H₆O₃ × 180.16 g C₉H₈O₄1 mol C₉H₈O₄ = 2.61 g theoretical
2.15 g C₉H₈O₄2.61 g C₉H₈O₄ × 100 = 82.4% (answer D)
A used the excess anhydride: 2.15/8.82 × 100 = 24.4%. B flipped the fraction: 2.61/2.15 × 100 = 121%. C dropped the × 100: 0.824.
Dr. Karmach

Practice 2: answer D

C₇H₆O₃ + C₄H₆O₃ → C₉H₈O₄ + C₂H₄O₂
given: 2.00 g C₇H₆O₃ and 5.00 g C₄H₆O₃ · actual: 2.15 g C₉H₈O₄ · C₇H₆O₃: 0.01448 ÷ 1 ← limits · C₄H₆O₃: 0.04898 ÷ 1, excess
2.00 g C₇H₆O₃ × 1 mol C₇H₆O₃138.12 g C₇H₆O₃ × 1 mol C₉H₈O₄1 mol C₇H₆O₃ × 180.16 g C₉H₈O₄1 mol C₉H₈O₄ = 2.61 g theoretical
2.15 g C₉H₈O₄2.61 g C₉H₈O₄ × 100 = 82.4% (answer D)
Below 100% ✓. Aspirin is recrystallized to purify it, and some stays dissolved in the rinse: the maximum comes from the limiting salicylic acid.
Dr. Karmach

Practice 3

CaC₂ + 2 H₂O → C₂H₂ + Ca(OH)₂

A miner's lamp drips water onto 12.8 g of CaC₂; water is in excess. The reaction runs at 80.0% yield. What mass of C₂H₂, in grams, does the lamp actually produce? (CaC₂ 64.10 g/mol · C₂H₂ 26.04 g/mol)

  1. 4.16
  2. 5.20
  3. 6.50
  4. 10.2
Dr. Karmach

Practice 3: answer A

CaC₂ + 2 H₂O → C₂H₂ + Ca(OH)₂
given: 12.8 g CaC₂, water in excess · percent yield: 80.0% · wanted: actual g C₂H₂
12.8 g CaC₂ × 1 mol CaC₂64.10 g CaC₂ × 1 mol C₂H₂1 mol CaC₂ × 26.04 g C₂H₂1 mol C₂H₂ = 5.20 g theoretical
actual = 80.0100 × 5.20 g = 4.16 g C₂H₂ (answer A)

B stopped at the theoretical yield: 5.20 g is the 100% mark, not what the lamp delivers. C divided by the yield instead of multiplying: 5.20 ÷ 0.800 = 6.50, more than the maximum. D applied the yield to the starting material: 12.8 × 0.800 = 10.2.

Dr. Karmach

Practice 3: answer A

CaC₂ + 2 H₂O → C₂H₂ + Ca(OH)₂
given: 12.8 g CaC₂, water in excess · percent yield: 80.0% · wanted: actual g C₂H₂
12.8 g CaC₂ × 1 mol CaC₂64.10 g CaC₂ × 1 mol C₂H₂1 mol CaC₂ × 26.04 g C₂H₂1 mol C₂H₂ = 5.20 g theoretical
actual = 80.0100 × 5.20 g = 4.16 g C₂H₂ (answer A)
Percent yield = actual ÷ theoretical × 100, solved for actual. An 80.0% yield must land below the 5.20 g maximum: 4.16 g ✓
Dr. Karmach

Check yourself

  1. Percent yield divides two masses. Which is computed, and which is read from the balance? (Which substance do both refer to?)
  2. Masses of two reactants are given, plus the product mass collected. List the steps from the given data to the percent yield. (Which reactant sets the 100% mark?)

Many of these reactions run in water, dosed by volume from a labeled solution. Molarity converts liters poured to moles delivered, the mole ratio takes over from there, and the same chains predict the product: solution stoichiometry.

Dr. Karmach

14 · Solution Stoichiometry

Convert a volume of solution to moles with molarity, cross substances with the mole ratio, and finish in grams or in the volume of a second solution.

Dr. Karmach

Dosed by volume

A pool is chlorinated by pumping in a measured volume of chlorine solution. Nothing is weighed: the strength on the drum's label and the liters pumped set the chlorine dose.

Dr. Karmach

A solution's label counts moles

0.500 M NaOH: 0.500 mol NaOH = 1 L of solution
the label states a rate: moles delivered per liter poured

Measure a volume, and the label converts it to moles; the liters cancel:

0.2000 L soln × 0.500 mol NaOH1 L soln = 0.100 mol NaOH

A graduated cylinder now counts moles. No balance is needed.

Dr. Karmach

Two ways to deliver 0.100 mol

A reaction receives 0.100 mol either way. Stoichiometry works on moles; where they came from never enters the calculation.

Dr. Karmach

Volume joins the map

Volume of solution enters through molarity, exactly where grams enter through molar mass. Every route still crosses the mole bridge, and the mole ratio still switches substances.

Dr. Karmach

The method

  1. Volume → moles: mL to L; molarity converts liters to moles of its solute.
  2. Moles → moles: cross substances with the mole ratio. No other step can.
  3. Moles → the wanted unit: molar mass for grams; molarity for volume.
Dr. Karmach

Worked example 1: moles from a solution volume

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂

Zinc metal dissolves in hydrochloric acid, releasing hydrogen gas. 250.0 mL of 0.400 M HCl reacts completely with excess zinc. How many moles of H₂ form?

Write the route first: mL → L → mol HCl → mol H₂.

Dr. Karmach

Worked example 1: solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂

Two conversion factors are needed.

Step 1 · Volume → moles

250.0 mL is 0.2500 L. The label's molarity converts the liters to moles of HCl:

0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Dr. Karmach

Worked example 1: solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂
Step 1 · Volume → moles
0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Step 2 · Moles → moles

The mole ratio, written H₂ over HCl (1 : 2), crosses substances; mol HCl cancels:

0.2500 L soln × 0.400 mol HCl1 L soln × 1 mol H₂2 mol HCl = 0.0500 mol H₂
Dr. Karmach

Worked example 1: solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂
Step 1 · Volume → moles
0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Step 2 · Moles → moles
0.2500 L soln × 0.400 mol HCl1 L soln × 1 mol H₂2 mol HCl = 0.0500 mol H₂
Each H₂ consumes two HCl, so the mole count halves: 0.100 mol HCl → 0.0500 mol H₂ ✓
Dr. Karmach

Worked example 1: the route on the map

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · found: 0.0500 mol H₂

A is HCl, B is H₂. Moles were wanted, so the route stops at mol B after the mole ratio. ✓
Dr. Karmach

Worked example 2: grams of product from a solution volume

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂

Two clear solutions mix, and bright yellow lead(II) iodide settles out. 150.0 mL of 0.300 M KI reacts completely with excess Pb(NO₃)₂. What mass of PbI₂ forms? (PbI₂ 461.0 g/mol)

A tempting shortcut: carry the moles of KI straight to grams of PbI₂. Test it against the equation.

Dr. Karmach

Worked example 2: solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)

Three conversion factors are needed.

Step 1 · Volume → moles

150.0 mL is 0.1500 L. The molarity, 0.300 mol per liter, converts the liters to 0.0450 mol KI.

Dr. Karmach

Worked example 2: solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗

mol KI cannot cancel mol PbI₂. The equation makes one PbI₂ from two KI; the mole ratio must cross first.

Dr. Karmach

Worked example 2: solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗
Step 2 · Moles → moles Step 3 · Moles → the wanted unit

The ratio, written PbI₂ over KI (1 : 2), crosses substances; the molar mass then converts out:

0.1500 L soln × 0.300 mol KI1 L soln × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 10.4 g PbI₂
Dr. Karmach

Worked example 2: solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗
Step 2 · Moles → moles Step 3 · Moles → the wanted unit
0.1500 L soln × 0.300 mol KI1 L soln × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 10.4 g PbI₂
Two KI deliver one PbI₂: 0.0450 mol halves to 0.0225 mol, and each mole weighs 461.0 g: about 10 g. 10.4 g ✓
Dr. Karmach

Worked example 2: the route on the map

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · found: 10.4 g PbI₂

A is KI, B is PbI₂. The tempting shortcut jumped from mol A to grams B, but no arrow joins them: every route crosses the mole ratio. ✓
Dr. Karmach

Your turn: copper(II) hydroxide

CuSO₄ + 2 NaOH → Cu(OH)₂ + Na₂SO₄
given: 200.0 mL (0.2000 L) of 0.250 M NaOH · wanted: g Cu(OH)₂ (97.57 g/mol)

Excess copper(II) sulfate reacts with 200.0 mL of 0.250 M NaOH, and pale blue Cu(OH)₂ precipitates:

0.2000 L soln × mol NaOH1 L soln × mol Cu(OH)₂ mol NaOH × g Cu(OH)₂1 mol Cu(OH)₂ = g Cu(OH)₂

Fill the molarity, the mole ratio, and the molar mass, then compute.

Dr. Karmach

Your turn: copper(II) hydroxide

CuSO₄ + 2 NaOH → Cu(OH)₂ + Na₂SO₄
given: 200.0 mL (0.2000 L) of 0.250 M NaOH · wanted: g Cu(OH)₂ (97.57 g/mol)
0.2000 L soln × mol NaOH1 L soln × mol Cu(OH)₂ mol NaOH × g Cu(OH)₂1 mol Cu(OH)₂ = g Cu(OH)₂
0.2000 L soln × 0.250 mol NaOH1 L soln × 1 mol Cu(OH)₂2 mol NaOH × 97.57 g Cu(OH)₂1 mol Cu(OH)₂ = 2.44 g Cu(OH)₂
Dr. Karmach

Where this goes wrong

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · correct: 0.1500 L → 0.0450 mol KI → 0.0225 mol PbI₂ → 10.4 g
Feeding milliliters to the molarity. 150.0 × 0.300 = 45.0 mol KI, a thousand times too many. Molarity counts liters of solution: 150.0 mL is 0.1500 L, and 0.1500 × 0.300 = 0.0450 mol.
Skipping the mole ratio. 0.0450 × 461.0 = 20.7 g assumes one PbI₂ per KI. The equation gives 1 PbI₂ : 2 KI, and only the mole ratio switches substances.
Inverting the ratio. (2 mol KI / 1 mol PbI₂) leaves mol KI uncancelled, and 0.0450 × 2 × 461.0 = 41.5 g is wrong. Write the wanted substance on top, so the given unit cancels.
Dr. Karmach

Practice 1

FeCl₃ + 3 NaOH → Fe(OH)₃ + 3 NaCl
molar mass Fe(OH)₃ 106.87 g/mol

300.0 mL of 0.200 M NaOH reacts completely with excess iron(III) chloride, and rust-brown Fe(OH)₃ precipitates. What mass of Fe(OH)₃, in grams, forms?

  1. 2.14
  2. 6.41
  3. 19.2
  4. 0.0200
Dr. Karmach

Practice 1: answer A

FeCl₃ + 3 NaOH → Fe(OH)₃ + 3 NaCl
given: 300.0 mL of 0.200 M NaOH · wanted: g Fe(OH)₃ (106.87 g/mol)
0.3000 L soln × 0.200 mol NaOH1 L soln × 1 mol Fe(OH)₃3 mol NaOH × 106.87 g Fe(OH)₃1 mol Fe(OH)₃ = 2.14 g Fe(OH)₃ (answer A)

B skipped the mole ratio: 0.0600 × 106.87 = 6.41. C inverted the ratio: 0.0600 × 3 × 106.87 = 19.2. D stopped at moles: 0.0600 × (1/3) = 0.0200 mol Fe(OH)₃, one factor short of grams.

0.0600 mol NaOH gives a third as many moles of Fe(OH)₃: 0.0200 mol, at about 107 g per mole: about 2 g. 2.14 g ✓
Dr. Karmach

Worked example 3: volume of a second solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 175.0 mL of 0.240 M NaOH · wanted: mL of 0.150 M H₂SO₄

A base spill of 175.0 mL of 0.240 M NaOH is neutralized with 0.150 M H₂SO₄ from the shelf. What volume of the acid solution, in milliliters, reacts completely?

Count the factors on the route: mL → L → mol NaOH → mol H₂SO₄ → L → mL.

Dr. Karmach

Worked example 3: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O

Three conversion factors are needed. Molarity works at both ends: the base's converts volume in to moles, the acid's converts moles out to volume.

Step 1 · Volume → moles

175.0 mL is 0.1750 L. The base's molarity converts the liters to moles of NaOH:

0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Dr. Karmach

Worked example 3: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles

The mole ratio, written H₂SO₄ over NaOH (1 : 2), gives 0.0210 mol H₂SO₄.

Dr. Karmach

Worked example 3: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles Step 3 · Moles → the wanted unit

The acid's molarity converts moles out to volume:

0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln × 1 mol H₂SO₄2 mol NaOH × 1 L acid soln0.150 mol H₂SO₄ = 0.140 L = 140. mL acid soln
Dr. Karmach

Worked example 3: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles Step 3 · Moles → the wanted unit
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln × 1 mol H₂SO₄2 mol NaOH × 1 L acid soln0.150 mol H₂SO₄ = 0.140 L = 140. mL acid soln
Half the moles (0.0210 vs 0.0420), but fewer per liter (0.150 vs 0.240): 140. mL is near 175.0 mL ✓
Dr. Karmach

Worked example 3: the route on the map

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 175.0 mL of 0.240 M NaOH · found: 140. mL of 0.150 M H₂SO₄

A is NaOH, B is H₂SO₄. Molarity works at both ends: the base's in, before the mole ratio, and the acid's out, after it. ✓
Dr. Karmach

Practice 2

Ba(OH)₂ + 2 HCl → BaCl₂ + 2 H₂O
two labeled solutions: 0.250 M Ba(OH)₂ · 0.400 M HCl

150.0 mL of 0.250 M Ba(OH)₂ reacts completely with 0.400 M HCl. What volume of the HCl solution, in milliliters, is required?

  1. 0.0750
  2. 46.9
  3. 93.8
  4. 188
Dr. Karmach

Practice 2: answer D

Ba(OH)₂ + 2 HCl → BaCl₂ + 2 H₂O
given: 150.0 mL of 0.250 M Ba(OH)₂ · wanted: mL of 0.400 M HCl
0.1500 L base soln × 0.250 mol Ba(OH)₂1 L base soln × 2 mol HCl1 mol Ba(OH)₂ × 1 L acid soln0.400 mol HCl = 0.1875 L = 188 mL (answer D)

A stopped at moles: 0.0375 × (2/1) = 0.0750 mol HCl, one factor short of a volume. B inverted the mole ratio: 0.0375 × 1/2 ÷ 0.400 = 0.0469 L, or 46.9 mL. C skipped the mole ratio: 0.0375 ÷ 0.400 = 0.0938 L, or 93.8 mL.

Two HCl are needed per Ba(OH)₂, and the acid is not twice as concentrated (0.400 vs 0.250 M), so the acid volume comes out larger: 188 mL vs 150.0 mL ✓
Dr. Karmach

Check yourself

  1. A bottle is labeled 2.00 M NaOH. Write the setup that converts 50.0 mL of this solution to moles of NaOH.
  2. In the route L of A → mol A → mol B → L of B, name the conversion factor at each arrow. Which one comes from the balanced equation?

This chain also runs backward: the volume of a known-molarity solution that reacts completely with an unknown gives the unknown's moles. That laboratory measurement is a titration.

Dr. Karmach

15 · Quantitative Analysis

Turn one careful measurement of a reaction (a titrant volume, a precipitate mass, trapped CO₂ and H₂O) into the unknown concentration, mass percent, or formula behind it.

Dr. Karmach

The chloride in a water sample

A water sample holds dissolved chloride no balance can weigh. Make it react into a solid, weigh that, and the equation reports what the water held.

Dr. Karmach

A reaction measures what it consumes

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
weighed: g AgCl on the balance · computed: g Cl⁻ that reacted · the mole ratio links them

A balanced equation ties every amount to every other amount. Measure any one of them, and stoichiometry computes the rest. Quantitative analysis is that strategy: react the unknown, measure something convenient.

Dr. Karmach

The same stoichiometry, started from a measurement

g A → mol A → mol B → g B
mass-to-mass stoichiometry: molar mass · mole ratio · molar mass
mL of titrant → mol titrant → mol unknown → molarity of the unknown
quantitative analysis: molarity · mole ratio · the sample's own volume

Mass-to-mass problems start from an amount someone chose. Quantitative analysis starts from an amount the lab measured. The mole ratio in the middle does not change.

Dr. Karmach

Three measurements, one skill

titration: volume of a known solution
a buret reads the volume that just completes the reaction · molarity converts it to moles
gravimetric analysis: mass of a precipitate
the unknown ion is collected as a weighable solid · molar mass converts it to moles
combustion analysis: masses of CO₂ and H₂O
a burned sample's carbon and hydrogen land in traps · each molar mass converts a gain to moles

Each technique measures one quantity and converts it to moles. From there every problem is the same stoichiometry.

Dr. Karmach

Titration counts moles with a buret

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
flask: the acid, amount unknown · buret: NaOH of known molarity (the titrant), volume read to 0.01 mL

Base flows in until an indicator's color just changes: the reaction is complete. The buret's volume reading becomes moles of acid.

Dr. Karmach

The method

Titration means stoichiometry so always start with a balanced chemical equation.

  1. Write the balanced equation.
  2. Convert the measurement to moles: molar mass or molarity.
  3. Cross to the unknown with the mole ratio.
  4. Report the asked-for form.
Dr. Karmach

The method on the map

Step 2 depends on what was measured. Step 4 depends on what the question asks. Step 3 is always the mole ratio from the balanced equation.

Dr. Karmach

Guided example: acid in an etching rinse

Step 1 · Write the balanced equation

HNO₃(aq) + NaOH(aq) → NaNO₃(aq) + H₂O(l)
measured: 18.40 mL of 0.500 M NaOH to the color change · wanted: mol HNO₃ in the flask

Rinse water from a metal-etching bath carries nitric acid. A sample is titrated with 0.500 M NaOH; the indicator changes color at 18.40 mL. How many moles of HNO₃ were in the flask?

On the map: the titration row, from mL of titrant to mol unknown.

Dr. Karmach

Guided example: solution

HNO₃(aq) + NaOH(aq) → NaNO₃(aq) + H₂O(l)
measured: 18.40 mL of 0.500 M NaOH · wanted: mol HNO₃

Two conversion factors are needed.

Step 2 · Convert the measurement to moles

Milliliters become liters first: 18.40 mL is 0.01840 L. The base's molarity converts the liters to moles:

0.01840 L NaOH soln × 0.500 mol NaOH1 L NaOH soln = 0.00920 mol NaOH
Dr. Karmach

Guided example: solution

HNO₃(aq) + NaOH(aq) → NaNO₃(aq) + H₂O(l)
measured: 18.40 mL of 0.500 M NaOH · wanted: mol HNO₃
Step 2 · Convert the measurement to moles
0.01840 L NaOH soln × 0.500 mol NaOH1 L NaOH soln = 0.00920 mol NaOH
Step 3 · Cross to the unknown with the mole ratio Step 4 · Report the asked-for form

The ratio, written HNO₃ over NaOH (1 : 1), crosses substances. The question asks for moles, so the route stops here:

0.00920 mol NaOH × 1 mol HNO₃1 mol NaOH = 0.00920 mol HNO₃
Dr. Karmach

Guided example: solution

HNO₃(aq) + NaOH(aq) → NaNO₃(aq) + H₂O(l)
measured: 18.40 mL of 0.500 M NaOH · wanted: mol HNO₃
Step 2 · Convert the measurement to moles
0.01840 L NaOH soln × 0.500 mol NaOH1 L NaOH soln = 0.00920 mol NaOH
Step 3 · Cross to the unknown with the mole ratio Step 4 · Report the asked-for form
0.00920 mol NaOH × 1 mol HNO₃1 mol NaOH = 0.00920 mol HNO₃
A fiftieth of a liter (20.00 mL) of 0.500 M base is 0.0100 mol; 18.40 mL is a little less, and one HNO₃ met each NaOH ✓
Dr. Karmach

Guided example: the route on the map

HNO₃(aq) + NaOH(aq) → NaNO₃(aq) + H₂O(l)
measured: 18.40 mL of 0.500 M NaOH · found: 0.00920 mol HNO₃

The titration row, Steps 2 and 3. The question asked for moles, so the molarity exit stays unused. ✓
Dr. Karmach

Worked example 1: an unknown acid concentration

Step 1 · Write the balanced equation

HCl + NaOH → NaCl + H₂O
given: 25.00 mL of HCl solution, molarity unknown · measured: 32.40 mL of 0.125 M NaOH to the color change

A stockroom bottle of hydrochloric acid lost its label. A 25.00 mL sample is titrated with 0.125 M NaOH; the indicator changes color at 32.40 mL. Find the molarity of the acid.

Write the route: mL of base → mol NaOH → mol HCl → M of the acid.

Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 25.00 mL acid sample · measured: 32.40 mL of 0.125 M NaOH · wanted: M of HCl

Two conversion factors are needed, then a division by the sample's own volume.

Step 2 · Convert the measurement to moles

32.40 mL is 0.03240 L. The base's molarity converts the liters to moles:

0.03240 L NaOH soln × 0.125 mol NaOH1 L NaOH soln = 0.00405 mol NaOH
Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 25.00 mL acid sample · measured: 32.40 mL of 0.125 M NaOH · wanted: M of HCl
Step 2 · Convert the measurement to moles
0.03240 L NaOH soln × 0.125 mol NaOH1 L NaOH soln = 0.00405 mol NaOH
Step 3 · Cross to the unknown with the mole ratio

The ratio, written HCl over NaOH (1 : 1), crosses substances: 0.00405 mol HCl sat in the flask.

Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 25.00 mL acid sample · measured: 32.40 mL of 0.125 M NaOH · wanted: M of HCl
Step 2 · Convert the measurement to moles
0.03240 L NaOH soln × 0.125 mol NaOH1 L NaOH soln = 0.00405 mol NaOH
Step 3 · Cross to the unknown with the mole ratio Step 4 · Report the asked-for form

Molarity is moles per liter of the acid's own 25.00 mL:

0.00405 mol HCl0.02500 L acid soln = 0.162 M HCl
Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 25.00 mL acid sample · measured: 32.40 mL of 0.125 M NaOH · wanted: M of HCl
Step 2 · Convert the measurement to moles
0.03240 L NaOH soln × 0.125 mol NaOH1 L NaOH soln = 0.00405 mol NaOH
Step 3 · Cross to the unknown with the mole ratio Step 4 · Report the asked-for form
0.00405 mol HCl0.02500 L acid soln = 0.162 M HCl
The acid needed more base volume than its own (32.40 vs 25.00 mL), so it packs more moles per liter than the base: 0.162 M vs 0.125 M ✓
Dr. Karmach

Worked example 1: the route on the map

HCl + NaOH → NaCl + H₂O
given: 25.00 mL acid sample · 32.40 mL of 0.125 M NaOH · found: 0.162 M HCl

All four steps of the titration row. Step 4 divides by the acid sample's 25.00 mL, never the buret's 32.40 mL. ✓
Dr. Karmach

Practice 1

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL of H₂SO₄ solution, molarity unknown · measured: 28.00 mL of 0.150 M NaOH to the color change

A 20.00 mL sample of diluted battery acid is titrated with 0.150 M NaOH; the indicator changes color at 28.00 mL. What is the molarity of the H₂SO₄?

  1. 0.420
  2. 0.105
  3. 0.210
  4. 0.00210
Dr. Karmach

Practice 1: answer B

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL acid sample · measured: 28.00 mL of 0.150 M NaOH · wanted: M of H₂SO₄
0.02800 L NaOH soln × 0.150 mol NaOH1 L NaOH soln × 1 mol H₂SO₄2 mol NaOH = 0.00210 mol H₂SO₄ · 0.00210 mol H₂SO₄0.02000 L acid soln = 0.105 M (answer B)

A flipped the mole ratio: 0.00840 ÷ 0.02000 = 0.420 M. C skipped the 2 : 1 ratio: 0.00420 ÷ 0.02000 = 0.210 M. D stopped at moles: 0.00210 mol H₂SO₄, never divided by the 0.02000 L sample.

Two NaOH per H₂SO₄: the acid holds half the base's moles, so 0.105 M sits below 0.150 M ✓
Dr. Karmach

Practice 1: the route on the map

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL acid sample · 28.00 mL of 0.150 M NaOH · found: 0.105 M H₂SO₄

The titration row, all four steps. Step 3 carries the equation's 1 H₂SO₄ : 2 NaOH, so the acid holds half the base's moles. ✓
Dr. Karmach

Gravimetric analysis: collect the ion as a solid

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
excess Ag⁺ leaves essentially no Cl⁻ behind in solution · the solid is filtered, dried, weighed

Excess reagent converts the ion completely into one insoluble solid. The dried precipitate's mass is the measurement; molar mass and mole ratio read the ion back out of it.

Dr. Karmach

Worked example 2: chloride in a de-icing blend

Step 1 · Write the balanced equation

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
given: 0.6250 g sample, dissolved · measured: dried AgCl 1.0260 g · wanted: mass % Cl⁻ = g Cl⁻ ÷ g sample × 100

A 0.6250 g sample of a road de-icing blend is dissolved in water; excess AgNO₃ precipitates the chloride. The dried AgCl weighs 1.0260 g. Find the mass percent of chloride in the blend. (AgCl 143.32 g/mol · Cl 35.45 g/mol)

The solid outweighs the sample it came from. The chloride percent must still land below 100.

Dr. Karmach

Worked example 2: grams of chloride

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
given: 0.6250 g sample · measured: 1.0260 g AgCl · wanted: mass % Cl⁻

Three conversion factors are needed, then the percent.

Step 2 · Convert the measurement to moles

The precipitate's molar mass converts its mass to moles:

1.0260 g AgCl × 1 mol AgCl143.32 g AgCl = 0.00716 mol AgCl
Dr. Karmach

Worked example 2: grams of chloride

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
given: 0.6250 g sample · measured: 1.0260 g AgCl · wanted: mass % Cl⁻
Step 2 · Convert the measurement to moles
1.0260 g AgCl × 1 mol AgCl143.32 g AgCl = 0.00716 mol AgCl
Step 3 · Cross to the unknown with the mole ratio

Each AgCl holds exactly one Cl⁻; the chloride's own molar mass then converts out to grams:

1.0260 g AgCl × 1 mol AgCl143.32 g AgCl × 1 mol Cl⁻1 mol AgCl × 35.45 g Cl⁻1 mol Cl⁻ = 0.2538 g Cl⁻
Dr. Karmach

Worked example 2: grams of chloride

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
given: 0.6250 g sample · measured: 1.0260 g AgCl · wanted: mass % Cl⁻
Step 2 · Convert the measurement to moles
1.0260 g AgCl × 1 mol AgCl143.32 g AgCl = 0.00716 mol AgCl
Step 3 · Cross to the unknown with the mole ratio
1.0260 g AgCl × 1 mol AgCl143.32 g AgCl × 1 mol Cl⁻1 mol AgCl × 35.45 g Cl⁻1 mol Cl⁻ = 0.2538 g Cl⁻
0.2538 g of chloride from 1.0260 g of solid: most of the precipitate's mass is the silver ✓
Dr. Karmach

Worked example 2: the percent

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
given: 0.6250 g sample · found: 0.2538 g Cl⁻ in the 1.0260 g of AgCl

Step 4 · Report the asked-for form

Mass percent compares the chloride's grams to the sample's:

0.2538 g Cl⁻0.6250 g sample × 100 = 40.6% Cl⁻
Dr. Karmach

Worked example 2: the percent

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
given: 0.6250 g sample · found: 0.2538 g Cl⁻ in the 1.0260 g of AgCl
Step 4 · Report the asked-for form
0.2538 g Cl⁻0.6250 g sample × 100 = 40.6% Cl⁻
Below 100 ✓. Only 35.45 of every 143.32 g of AgCl is chloride, so 1.0260 g of solid holds just 0.2538 g of Cl⁻. Pure NaCl would be 60.7% chloride; this blend, with non-chloride components, lands lower.

Dr. Karmach

Your turn: sulfate in a fertilizer

Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s)
given: 0.8000 g fertilizer, dissolved · measured: dried BaSO₄ 0.5580 g · wanted: mass % SO₄²⁻

Excess BaCl₂ precipitates the sulfate from a dissolved 0.8000 g fertilizer sample; the dried BaSO₄ weighs 0.5580 g. (BaSO₄ 233.39 g/mol · SO₄²⁻ 96.06 g/mol)

0.5580 g BaSO₄ × 1 mol BaSO₄ g BaSO₄ × 1 mol SO₄²⁻1 mol BaSO₄ × g SO₄²⁻1 mol SO₄²⁻ = g SO₄²⁻ · g SO₄²⁻0.8000 g sample × 100 =

Fill the two molar masses, the grams of sulfate, then the percent.

Dr. Karmach

Your turn: sulfate in a fertilizer

Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s)
given: 0.8000 g fertilizer, dissolved · measured: dried BaSO₄ 0.5580 g · wanted: mass % SO₄²⁻
0.5580 g BaSO₄ × 1 mol BaSO₄ g BaSO₄ × 1 mol SO₄²⁻1 mol BaSO₄ × g SO₄²⁻1 mol SO₄²⁻ = g SO₄²⁻ · g SO₄²⁻0.8000 g sample × 100 =
0.5580 g BaSO₄ × 1 mol BaSO₄233.39 g BaSO₄ × 1 mol SO₄²⁻1 mol BaSO₄ × 96.06 g SO₄²⁻1 mol SO₄²⁻ = 0.2297 g SO₄²⁻ · 0.2297 g SO₄²⁻0.8000 g sample × 100 = 28.7%
Dr. Karmach

Practice 2

Ca²⁺(aq) + CO₃²⁻(aq) → CaCO₃(s)
given: 1.2500 g sample, dissolved · measured: dried CaCO₃ 0.6900 g · CaCO₃ 100.09 g/mol · Ca 40.08 g/mol

A 1.2500 g sample of a mineral supplement is dissolved, and excess sodium carbonate precipitates the calcium as CaCO₃. The dried solid weighs 0.6900 g. What is the mass percent of calcium in the sample?

  1. 55.20
  2. 22.10
  3. 137.8
  4. 0.2763
  5. 40.04
Dr. Karmach

Practice 2: answer B

Ca²⁺(aq) + CO₃²⁻(aq) → CaCO₃(s)
given: 1.2500 g sample · measured: 0.6900 g CaCO₃ · wanted: mass % Ca²⁺
0.6900 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol Ca²⁺1 mol CaCO₃ × 40.08 g Ca²⁺1 mol Ca²⁺ = 0.2763 g Ca²⁺ · 0.2763 g Ca²⁺1.2500 g sample × 100 = 22.10% (answer B)
Dr. Karmach

Practice 2: answer B

Ca²⁺(aq) + CO₃²⁻(aq) → CaCO₃(s)
given: 1.2500 g sample · measured: 0.6900 g CaCO₃ · wanted: mass % Ca²⁺
0.6900 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol Ca²⁺1 mol CaCO₃ × 40.08 g Ca²⁺1 mol Ca²⁺ = 0.2763 g Ca²⁺ · 0.2763 g Ca²⁺1.2500 g sample × 100 = 22.10% (answer B)
A took the whole precipitate as calcium: 0.6900 ÷ 1.2500 × 100 = 55.20. C flipped the ion factor: 0.6900 × 100.09 ÷ 40.08 makes 1.7231 g of calcium out of 0.6900 g of solid, 137.8% of the sample. D stopped at the mass of calcium, 0.2763 g, before dividing by the 1.2500 g sample. E is calcium's share of the precipitate, 40.08 ÷ 100.09 × 100 = 40.04, not of the sample.
Dr. Karmach

Practice 2: answer B

Ca²⁺(aq) + CO₃²⁻(aq) → CaCO₃(s)
given: 1.2500 g sample · measured: 0.6900 g CaCO₃ · wanted: mass % Ca²⁺
0.6900 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol Ca²⁺1 mol CaCO₃ × 40.08 g Ca²⁺1 mol Ca²⁺ = 0.2763 g Ca²⁺ · 0.2763 g Ca²⁺1.2500 g sample × 100 = 22.10% (answer B)
CaCO₃ is 40.04% calcium, so the 0.6900 g of solid holds 0.2763 g of it, about a fifth of the 1.2500 g sample ✓

Dr. Karmach

Combustion analysis: traps sort the atoms

Burned in excess oxygen, a compound of carbon and hydrogen releases every C atom as CO₂ and every H atom in H₂O. Each trap's gain in mass measures one element.

Dr. Karmach

Worked example 3: a hydrocarbon's empirical formula

Step 1 · Write the balanced equation

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
measured: CO₂ trap +0.8800 g · H₂O trap +0.3604 g · sample burned: 0.2805 g · wanted: empirical formula

A 0.2805 g sample of a fuel gas containing only carbon and hydrogen burns completely. The CO₂ trap gains 0.8800 g; the H₂O trap gains 0.3604 g. Find the empirical formula. (CO₂ 44.01 · H₂O 18.02 g/mol)

Write the route: g CO₂ → mol C, g H₂O → mol H, then the smallest whole-number ratio.

Dr. Karmach

Worked example 3: moles of C and H

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
measured: +0.8800 g CO₂ · +0.3604 g H₂O · sample: 0.2805 g · wanted: empirical formula

Two conversion chains run in parallel, one per element; each runs both steps in one pass.

Step 2 · Convert the measurement to moles Step 3 · Cross to the unknown with the mole ratio

Carbon first: the trap's own molar mass converts the gain to moles, and each CO₂ carries one C:

0.8800 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.02000 mol C
Dr. Karmach

Worked example 3: moles of C and H

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
measured: +0.8800 g CO₂ · +0.3604 g H₂O · sample: 0.2805 g · wanted: empirical formula
Step 2 · Convert the measurement to moles Step 3 · Cross to the unknown with the mole ratio
0.8800 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.02000 mol C
The hydrogen chain

Each H₂O carries two H:

0.3604 g H₂O × 1 mol H₂O18.02 g H₂O × 2 mol H1 mol H₂O = 0.04000 mol H
Dr. Karmach

Worked example 3: moles of C and H

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
measured: +0.8800 g CO₂ · +0.3604 g H₂O · sample: 0.2805 g · wanted: empirical formula
Step 2 · Convert the measurement to moles Step 3 · Cross to the unknown with the mole ratio
0.8800 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.02000 mol C
The hydrogen chain
0.3604 g H₂O × 1 mol H₂O18.02 g H₂O × 2 mol H1 mol H₂O = 0.04000 mol H
0.02000 mol C and 0.04000 mol H: twice as many hydrogen atoms as carbon ✓
Dr. Karmach

Worked example 3: the formula finish

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
found: 0.02000 mol C · 0.04000 mol H · sample: 0.2805 g · wanted: empirical formula

Step 4 · Report the asked-for form

Divide by the smaller count, exactly as with percent-composition data:

C: 0.02000 mol0.02000 = 1.00 · H: 0.04000 mol0.02000 = 2.00 = CH₂
Dr. Karmach

Worked example 3: the formula finish

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
found: 0.02000 mol C · 0.04000 mol H · sample: 0.2805 g · wanted: empirical formula
Step 4 · Report the asked-for form
C: 0.02000 mol0.02000 = 1.00 · H: 0.04000 mol0.02000 = 2.00 = CH₂
Mass check: 0.02000 mol C weighs 0.2402 g, 0.04000 mol H weighs 0.0403 g; together 0.2805 g, the whole sample, so no other element hides in it ✓. Here the division came out 2.00; a ratio that lands on 1.33 is the fraction 4/3, and multiplying every count by 3 clears it, the same multiply-to-whole finish that turns percent-composition data into formulas. A measured molar mass of 28.05 g/mol would scale CH₂ to C₂H₄.

Dr. Karmach

Where this goes wrong

Reporting the precipitate's percent. 1.0260 g of AgCl from a 0.6250 g sample reads 1.0260 ÷ 0.6250 × 100 = 164.2%, more chloride than sample. The silver's mass came from the added reagent. Only 35.45 of every 143.32 g of AgCl is chloride: 0.2538 g, and 40.6%.
Taking a trap's gain as the element's mass. The CO₂ trap gained 0.8800 g, but that mass is carbon plus oxygen. Carbon is 12.01 of every 44.01 g: 0.8800 × 12.01 ÷ 44.01 = 0.2402 g C.
Forgetting each H₂O carries two H. 0.3604 g of H₂O is 0.02000 mol H₂O but 0.04000 mol H. Counting 0.02000 mol H turns CH₂ into CH, a different compound.
Dividing by the titrant's volume. 0.00405 mol HCl ÷ 0.03240 L gives 0.125 M, the base's own molarity back again. The unknown's molarity divides by the unknown's volume: 0.00405 ÷ 0.02500 = 0.162 M.
Dr. Karmach

Practice 3

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
measured: CO₂ trap +1.0562 g · H₂O trap +0.5766 g · CO₂ 44.01 · H₂O 18.02 g/mol

A camp-stove fuel contains only carbon and hydrogen. Complete combustion of a sample sends 1.0562 g into the CO₂ trap and 0.5766 g into the H₂O trap. What is the empirical formula?

  1. C₃H₈
  2. CH₃
  3. C₃H₄
  4. C₈H₃
Dr. Karmach

Practice 3: answer A

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
measured: +1.0562 g CO₂ · +0.5766 g H₂O · wanted: empirical formula
1.0562 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.02400 mol C · 0.5766 g H₂O × 1 mol H₂O18.02 g H₂O × 2 mol H1 mol H₂O = 0.06400 mol H · C: 0.02400 ÷ 0.02400 = 1.00 · H: 0.06400 ÷ 0.02400 = 2.67 · × 3 → C 3.00, H 8.00 = C₃H₈ (answer A)
Dr. Karmach

Practice 3: answer A

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
measured: +1.0562 g CO₂ · +0.5766 g H₂O · wanted: empirical formula
1.0562 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.02400 mol C · 0.5766 g H₂O × 1 mol H₂O18.02 g H₂O × 2 mol H1 mol H₂O = 0.06400 mol H · C: 0.02400 ÷ 0.02400 = 1.00 · H: 0.06400 ÷ 0.02400 = 2.67 · × 3 → C 3.00, H 8.00 = C₃H₈ (answer A)
B rounded 2.67 up to 3, and CH₃ claims more hydrogen than the traps caught. C forgot the 2 in each H₂O: 0.5766 ÷ 18.02 = 0.03200 mol H gives 0.03200 ÷ 0.02400 = 1.33, and × 3 → C₃H₄. D crossed the counts: carbon's 0.02400 mol is the smaller count, so carbon takes the smaller subscript.
Dr. Karmach

Practice 3: answer A

CxHy + O₂ (excess) → x CO₂ + y/2 H₂O
measured: +1.0562 g CO₂ · +0.5766 g H₂O · wanted: empirical formula
1.0562 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.02400 mol C · 0.5766 g H₂O × 1 mol H₂O18.02 g H₂O × 2 mol H1 mol H₂O = 0.06400 mol H · C: 0.02400 ÷ 0.02400 = 1.00 · H: 0.06400 ÷ 0.02400 = 2.67 · × 3 → C 3.00, H 8.00 = C₃H₈ (answer A)
2.67 is the fraction 8⁄3, and × 3 clears it. C₃H₈ is propane, a real camp-stove fuel ✓

Dr. Karmach

Worked example 4: a redox titration to a mass percent

Step 1 · Write the balanced equation

2 MnO₄⁻ + 6 H⁺ + 5 H₂C₂O₄ → 2 Mn²⁺ + 10 CO₂ + 8 H₂O
given: 1.00 g sample, dissolved · measured: 24.0 mL of 0.0100 M KMnO₄ · wanted: mass % H₂C₂O₄ (90.04 g/mol)

Rust remover is largely oxalic acid, H₂C₂O₄. A 1.00 g sample is dissolved and titrated with 0.0100 M KMnO₄; the purple color first persists at 24.0 mL. Find the mass percent of oxalic acid.

The titrant is a redox reagent, not a base. The route does not change: mL of titrant → mol MnO₄⁻ → mol H₂C₂O₄ → g → percent.

Dr. Karmach

Worked example 4: grams of oxalic acid

2 MnO₄⁻ + 6 H⁺ + 5 H₂C₂O₄ → 2 Mn²⁺ + 10 CO₂ + 8 H₂O

Step 2 · Convert the measurement to moles

24.0 mL is 0.0240 L. The titrant's molarity converts the liters to moles:

0.0240 L soln × 0.0100 mol MnO₄⁻1 L soln = 0.000240 mol MnO₄⁻
Dr. Karmach

Worked example 4: grams of oxalic acid

2 MnO₄⁻ + 6 H⁺ + 5 H₂C₂O₄ → 2 Mn²⁺ + 10 CO₂ + 8 H₂O
Step 2 · Convert the measurement to moles
0.0240 L soln × 0.0100 mol MnO₄⁻1 L soln = 0.000240 mol MnO₄⁻
Step 3 · Cross to the unknown with the mole ratio

The ratio, H₂C₂O₄ over MnO₄⁻ (5 : 2), crosses substances; the molar mass converts out:

0.000240 mol MnO₄⁻ × 5 mol H₂C₂O₄2 mol MnO₄⁻ × 90.04 g H₂C₂O₄1 mol H₂C₂O₄ = 0.0540 g H₂C₂O₄
Dr. Karmach

Worked example 4: grams of oxalic acid

2 MnO₄⁻ + 6 H⁺ + 5 H₂C₂O₄ → 2 Mn²⁺ + 10 CO₂ + 8 H₂O
Step 2 · Convert the measurement to moles
0.0240 L soln × 0.0100 mol MnO₄⁻1 L soln = 0.000240 mol MnO₄⁻
Step 3 · Cross to the unknown with the mole ratio

The ratio, H₂C₂O₄ over MnO₄⁻ (5 : 2), crosses substances; the molar mass converts out:

0.000240 mol MnO₄⁻ × 5 mol H₂C₂O₄2 mol MnO₄⁻ × 90.04 g H₂C₂O₄1 mol H₂C₂O₄ = 0.0540 g H₂C₂O₄
More acid than titrant: 5/2 × 0.000240 = 0.000600 mol, so a few hundredths of a gram ✓
Dr. Karmach

Worked example 4: the percent

Step 4 · Report the asked-for form

0.0540 g H₂C₂O₄1.00 g sample × 100 = 5.40% H₂C₂O₄
Dr. Karmach

Worked example 4: the percent

Step 4 · Report the asked-for form

0.0540 g H₂C₂O₄1.00 g sample × 100 = 5.40% H₂C₂O₄
MnO₄⁻ is its own indicator: the first unconsumed drop stays purple. Below 100 ✓.

Dr. Karmach

Take-home: weigh the solid, report the ion

1.0260 g AgCl ÷ 0.6250 g sample × 100 = 164.2% ✗
more chloride than sample is impossible · the silver's mass came from the added reagent
1.0260 g AgCl → 0.2538 g Cl⁻ · 0.2538 ÷ 0.6250 × 100 = 40.6% ✓
molar mass and mole ratio extract the ion's share first

The balance weighs the whole precipitate. The unknown ion is only part of it. Convert through moles before any percent.

Dr. Karmach

Worked example 5: calcium in an antacid tablet

Step 1 · Write the balanced equation

Ca²⁺(aq) + C₂O₄²⁻(aq) + H₂O(l) → CaC₂O₄·H₂O(s)
given: 2.500 g tablet, dissolved · measured: crucible 24.0314 g empty, 25.4600 g with dried solid · wanted: mass % Ca (CaC₂O₄·H₂O 146.12 g/mol · Ca 40.08 g/mol)

An antacid tablet weighing 2.500 g is dissolved and its calcium precipitated as the hydrate CaC₂O₄·H₂O. The dried solid is weighed in its crucible: 24.0314 g empty, 25.4600 g with the solid. Find the mass percent of calcium.

No balance weighs the precipitate alone. Two readings, subtracted, do.

Dr. Karmach

Worked example 5: grams of calcium

Ca²⁺(aq) + C₂O₄²⁻(aq) + H₂O(l) → CaC₂O₄·H₂O(s)
measured: 24.0314 g empty, 25.4600 g with solid · sample: 2.500 g · wanted: mass % Ca

The measurement, by difference

The crucible readings subtract: 25.4600 g − 24.0314 g = 1.4286 g of dried CaC₂O₄·H₂O.

Dr. Karmach

Worked example 5: grams of calcium

Ca²⁺(aq) + C₂O₄²⁻(aq) + H₂O(l) → CaC₂O₄·H₂O(s)
measured: 24.0314 g empty, 25.4600 g with solid · sample: 2.500 g · wanted: mass % Ca
The measurement, by difference Step 2 · Convert the measurement to moles Step 3 · Cross to the unknown with the mole ratio

The hydrate's molar mass includes its water: 40.08 + 24.02 + 64.00 + 18.02 = 146.12 g/mol. Each formula unit holds one Ca:

1.4286 g CaC₂O₄·H₂O × 1 mol CaC₂O₄·H₂O146.12 g CaC₂O₄·H₂O × 1 mol Ca1 mol CaC₂O₄·H₂O × 40.08 g Ca1 mol Ca = 0.3919 g Ca
Dr. Karmach

Worked example 5: grams of calcium

Ca²⁺(aq) + C₂O₄²⁻(aq) + H₂O(l) → CaC₂O₄·H₂O(s)
measured: 24.0314 g empty, 25.4600 g with solid · sample: 2.500 g · wanted: mass % Ca
The measurement, by difference Step 2 · Convert the measurement to moles Step 3 · Cross to the unknown with the mole ratio
1.4286 g CaC₂O₄·H₂O × 1 mol CaC₂O₄·H₂O146.12 g CaC₂O₄·H₂O × 1 mol Ca1 mol CaC₂O₄·H₂O × 40.08 g Ca1 mol Ca = 0.3919 g Ca
Of the hydrate's 146.12 g/mol, only 40.08 g is calcium: the oxalate and its water carry most of the solid's mass, so 1.4286 g of solid holds just 0.3919 g of Ca ✓
Dr. Karmach

Worked example 5: the percent

Ca²⁺(aq) + C₂O₄²⁻(aq) + H₂O(l) → CaC₂O₄·H₂O(s)
sample: 2.500 g · found: 0.3919 g Ca in the 1.4286 g of dried solid

Step 4 · Report the asked-for form

Mass percent compares the calcium's grams to the tablet's:

0.3919 g Ca2.500 g sample × 100 = 15.7% Ca
Dr. Karmach

Worked example 5: the percent

Ca²⁺(aq) + C₂O₄²⁻(aq) + H₂O(l) → CaC₂O₄·H₂O(s)
sample: 2.500 g · found: 0.3919 g Ca in the 1.4286 g of dried solid
Step 4 · Report the asked-for form
0.3919 g Ca2.500 g sample × 100 = 15.7% Ca
Pure calcium carbonate is 40.08 ÷ 100.09 × 100 = 40.0% Ca; a tablet padded with binders and flavor lands lower. Dropping the ·H₂O from the molar mass would overcount the calcium. ✓

Dr. Karmach

Worked example 6: combustion with oxygen in the sample

Step 1 · Write the balanced equation

CxHyOz + O₂ (excess) → x CO₂ + y/2 H₂O
measured: 0.225 g sample · CO₂ trap +0.512 g · H₂O trap +0.209 g · wanted: empirical formula (CO₂ 44.01 · H₂O 18.02 · C 12.01 · H 1.008 · O 16.00 g/mol)

A 0.225 g sample of a solvent containing carbon, hydrogen, and oxygen burns completely. The CO₂ trap gains 0.512 g; the H₂O trap gains 0.209 g. Find the empirical formula.

The traps still catch every C and every H. The sample's own oxygen mixes into the O₂ stream, so no trap can count it: its mass comes by subtraction.

Dr. Karmach

Worked example 6: carbon and hydrogen first

CxHyOz + O₂ (excess) → x CO₂ + y/2 H₂O

Step 2 · Convert the measurement to moles Step 3 · Cross to the unknown with the mole ratio

0.512 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.01163 mol C · × 12.01 g/mol = 0.1397 g C
Dr. Karmach

Worked example 6: carbon and hydrogen first

CxHyOz + O₂ (excess) → x CO₂ + y/2 H₂O

Step 2 · Convert the measurement to moles Step 3 · Cross to the unknown with the mole ratio

0.512 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.01163 mol C · × 12.01 g/mol = 0.1397 g C
0.209 g H₂O × 1 mol H₂O18.02 g H₂O × 2 mol H1 mol H₂O = 0.02320 mol H · × 1.008 g/mol = 0.0234 g H
Dr. Karmach

Worked example 6: carbon and hydrogen first

CxHyOz + O₂ (excess) → x CO₂ + y/2 H₂O

Step 2 · Convert the measurement to moles Step 3 · Cross to the unknown with the mole ratio

0.512 g CO₂ × 1 mol CO₂44.01 g CO₂ × 1 mol C1 mol CO₂ = 0.01163 mol C · × 12.01 g/mol = 0.1397 g C
0.209 g H₂O × 1 mol H₂O18.02 g H₂O × 2 mol H1 mol H₂O = 0.02320 mol H · × 1.008 g/mol = 0.0234 g H
C and H carry 0.1397 + 0.0234 = 0.1631 g of the 0.225 g burned: the shortfall is oxygen. ✓
Dr. Karmach

Worked example 6: oxygen by subtraction

CxHyOz + O₂ (excess) → x CO₂ + y/2 H₂O
sample: 0.225 g · found: 0.1397 g C (0.01163 mol) · 0.0234 g H (0.02320 mol)
mass O: 0.225 − 0.1397 − 0.0234 = 0.0619 g · 0.0619 g O16.00 g/mol = 0.00387 mol O
Dr. Karmach

Worked example 6: oxygen by subtraction

CxHyOz + O₂ (excess) → x CO₂ + y/2 H₂O
sample: 0.225 g · found: 0.1397 g C (0.01163 mol) · 0.0234 g H (0.02320 mol)
mass O: 0.225 − 0.1397 − 0.0234 = 0.0619 g · 0.0619 g O16.00 g/mol = 0.00387 mol O
Step 4 · Report the asked-for form
C: 0.011630.00387 = 3.01 · H: 0.023200.00387 = 5.99 · O: 0.003870.00387 = 1.00 = C₃H₆O
Dr. Karmach

Worked example 6: oxygen by subtraction

CxHyOz + O₂ (excess) → x CO₂ + y/2 H₂O
sample: 0.225 g · found: 0.1397 g C (0.01163 mol) · 0.0234 g H (0.02320 mol)
mass O: 0.225 − 0.1397 − 0.0234 = 0.0619 g · 0.0619 g O16.00 g/mol = 0.00387 mol O
Step 4 · Report the asked-for form
C: 0.011630.00387 = 3.01 · H: 0.023200.00387 = 5.99 · O: 0.003870.00387 = 1.00 = C₃H₆O
C₃H₆O is acetone's formula, a common lab solvent ✓. Reading the sample's oxygen from the traps would count oxygen that arrived with the O₂ stream; only the subtraction isolates the sample's own.
Dr. Karmach

Check yourself

  1. A dissolved sample gives 0.4120 g of dried AgCl. State the steps that turn that one mass into the mass percent of chloride in the sample. Which factor comes from the balanced equation?
  2. A burned hydrocarbon gives 0.030 mol of CO₂ and 0.020 mol of H₂O. Which element has more moles of atoms in the compound? Compute both counts.

Titration returns with the study of solutions: the exact moment the indicator flips is the equivalence point, and acids that release two or three H⁺ per formula unit change the mole ratio. The divide-by-smallest, multiply-to-whole finish is the same one that turns percent-composition data into formulas.

Dr. Karmach

Can you…?

  • ☐ balance any chemical equation with the smallest whole-number coefficients?
  • ☐ read a balanced equation as a recipe: coefficients are mole relationships?
  • ☐ convert between amounts of any two species using mole ratios?
  • ☐ chain molar masses with mole ratios to solve gram-to-gram problems?
  • ☐ identify which reactant limits a reaction and how much product it allows?
  • ☐ classify a reaction by type and cite the evidence that a reaction occurred?
  • ☐ apply the solubility rules to predict precipitates and assign physical states?
  • ☐ write molecular, complete ionic, and net ionic equations and classify electrolytes?
  • ☐ assign oxidation numbers and identify oxidizing and reducing agents?
  • ☐ write half-reactions and use the activity series to predict single displacement?
  • ☐ carry molarity through stoichiometric calculations and compute percent yield?
  • ☐ find an unknown concentration, mass percent, or formula from one measurement?

If any box stays empty, the practice site has a drill for it. 🧪

Dr. Karmach

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