Solutions

General Chemistry · Dr. Karmach

Dr. Karmach

By the end of this unit, you can…

  • Explain "like dissolves like" and predict whether a solute dissolves in a given solvent
  • Describe unsaturated, saturated, and supersaturated solutions; read a solubility curve
  • Use the dilution relation M₁V₁ = M₂V₂ to find a concentration or volume
  • Calculate molality and mole fraction, and convert among molarity, molality, and mass percent
  • Classify a mixture as a solution, a colloid, or a suspension from particle size, light scattering, and settling, and name a colloid's type from its dispersed phase and medium
  • Apply colligative properties (freezing-point depression, boiling-point elevation, and Raoult's law) using the van't Hoff factor
  • Apply Henry's law to gas solubility and titration stoichiometry to find an unknown concentration
Dr. Karmach

Today's route 🗺️

  1. Like Dissolves Like
  2. Saturation & Solubility Curves
  3. Dilution
  4. Molality & Mole Fraction
  5. Converting Concentration Units
  6. Colloids
  7. Freezing Point & Boiling Point
  8. Raoult's Law
  9. Henry's Law
  10. Titration Calculations
Dr. Karmach

1 · Like Dissolves Like

Predict whether a solute dissolves in a given solvent by matching their attractions: polar and ionic solutes dissolve in polar solvents, nonpolar solutes in nonpolar solvents.

Dr. Karmach

Why oil won't mix but sugar vanishes

Shake oil and vinegar and they split back into two layers every time. Stir sugar into hot tea and it disappears completely.

Dr. Karmach

A solute dissolves by replacing attractions

The solute is what dissolves; the solvent is what it dissolves into. A solute dissolves only when new solute–solvent attractions can replace the solute–solute attractions being broken.

Dr. Karmach

Like dissolves like

Attractions match only when polarities match. A polar or ionic solute dissolves in a polar solvent like water. A nonpolar solute dissolves in a nonpolar solvent like oil or hexane.

memory hook: water loves charge, oil loves oil
polar and ionic go with polar · nonpolar goes with nonpolar · a mismatch stays in two layers
Dr. Karmach

Why oil and water separate

Water molecules hold one another with strong hydrogen bonds. A nonpolar oil molecule attracts only weakly, too weak to enter that network. So the oil is pushed out into its own layer.

Dr. Karmach

The method

  1. Find the solute's polarity. Ionic or polar, or nonpolar?
  2. Find the solvent's polarity. Polar like water, or nonpolar like oil or hexane?
  3. Match them. Same family dissolves. A mismatch stays separate.
Dr. Karmach

Worked example 1: table salt in water

table salt (NaCl) stirred into water
ionic solid · 58.44 g/mol · water is a polar solvent

Table salt is an ionic solid, and water is a polar solvent. Predict whether the salt dissolves, and why.

Dr. Karmach

Worked example 1: solution

table salt (NaCl) stirred into water
ionic solid · 58.44 g/mol · water is a polar solvent

Step 1 · Find the solute's polarity

Salt is built from Na⁺ and Cl⁻ ions. Their charge attracts polar molecules strongly, so ionic solutes belong with the polar family.

Dr. Karmach

Worked example 1: solution

table salt (NaCl) stirred into water
ionic solid · 58.44 g/mol · water is a polar solvent
Step 1 · Find the solute's polarity Step 2 · Find the solvent's polarity

Water is polar. Each molecule has a positive end and a negative end that can turn toward a charge.

Dr. Karmach

Worked example 1: solution

table salt (NaCl) stirred into water
ionic solid · 58.44 g/mol · water is a polar solvent
Step 1 · Find the solute's polarity Step 2 · Find the solvent's polarity Step 3 · Match them
ionic solute · polar solvent → same family, it dissolves

Water molecules surround each ion, their charged ends replacing the pull the ions had on one another.

Dr. Karmach

Worked example 1: solution

table salt (NaCl) stirred into water
ionic solid · 58.44 g/mol · water is a polar solvent
Step 1 · Find the solute's polarity Step 2 · Find the solvent's polarity Step 3 · Match them
ionic solute · polar solvent → same family, it dissolves
The new ion–water attractions are as strong as the ones inside the salt, so the crystal comes apart and dissolves.
Dr. Karmach

Worked example 1: the route on the map

table salt (NaCl) stirred into water
ionic solute · polar solvent · found: it dissolves

An ionic solute sits in the polar family, the same family as water. Same family: it dissolves. ✓
Dr. Karmach

Worked example 2: cooking grease in water

cooking grease rinsed with cold water
nonpolar solute · solvent: water, polar

Grease is nonpolar, and you try to rinse a greasy pan with plain cold water.

A common first answer: water dissolves so much that enough of it must wash the grease away. Test it against the method.

Dr. Karmach

Worked example 2: solution

cooking grease rinsed with cold water
nonpolar solute · solvent: water, polar

A common first answer

enough water washes the grease away?
water dissolves polar and ionic things, not nonpolar grease ✗

Water dissolves a lot, but only polar and ionic solutes. Adding more water changes nothing here.

Dr. Karmach

Worked example 2: solution

cooking grease rinsed with cold water
nonpolar solute · solvent: water, polar
A common first answer
enough water washes the grease away?
water dissolves polar and ionic things, not nonpolar grease ✗
Step 1 · Find the solute's polarity

Grease is a nonpolar mix of oils. Its molecules attract each other only weakly and carry no charge.

Dr. Karmach

Worked example 2: solution

cooking grease rinsed with cold water
nonpolar solute · solvent: water, polar
A common first answer
enough water washes the grease away?
water dissolves polar and ionic things, not nonpolar grease ✗
Step 1 · Find the solute's polarity Step 2 · Find the solvent's polarity

Water is polar, and holds itself together with strong hydrogen bonds.

Dr. Karmach

Worked example 2: solution

cooking grease rinsed with cold water
nonpolar solute · solvent: water, polar
A common first answer
enough water washes the grease away?
water dissolves polar and ionic things, not nonpolar grease ✗
Step 1 · Find the solute's polarity Step 2 · Find the solvent's polarity Step 3 · Match them
nonpolar solute · polar solvent → a mismatch, it stays separate

Water's hydrogen bonds to itself are far stronger than its weak attraction to the grease, so the grease is left untouched.

Dr. Karmach

Worked example 2: solution

cooking grease rinsed with cold water
nonpolar solute · solvent: water, polar
A common first answer
enough water washes the grease away?
water dissolves polar and ionic things, not nonpolar grease ✗
Step 1 · Find the solute's polarity Step 2 · Find the solvent's polarity Step 3 · Match them
nonpolar solute · polar solvent → a mismatch, it stays separate
The attraction between grease and water is far weaker than water's attraction to itself. The grease beads up and stays put, however much water runs over it.
Dr. Karmach

Worked example 2: the route on the map

cooking grease rinsed with cold water
nonpolar solute · polar solvent · found: it stays separate

Grease sits in the nonpolar family, water in the polar family. A mismatch leaves two layers. ✓
Dr. Karmach

Take-home: water is not a universal solvent

salt · sugar · vinegar: dissolve in water
polar and ionic solutes: water's charged ends attract them
oil · grease · wax: do not dissolve in water
nonpolar solutes: water bonds to itself and leaves them out

Water dissolves polar and ionic solutes, not everything. A nonpolar solute cannot replace the strong hydrogen bonds between water molecules, so it stays separate however much water is present.

Dr. Karmach

Your turn: candle wax in water

a chip of candle wax dropped into water
wax is nonpolar · water is a polar solvent
step question answer
1 · solute polarity polar/ionic, or nonpolar? wax is
2 · solvent polarity polar or nonpolar? water is
3 · match them same family, or a mismatch?

Fill the three cells, then read off the result.

Dr. Karmach

Your turn: candle wax in water

a chip of candle wax dropped into water
wax is nonpolar · water is a polar solvent
step question answer
1 · solute polarity polar/ionic, or nonpolar? wax is
2 · solvent polarity polar or nonpolar? water is
3 · match them same family, or a mismatch?

Fill the three cells, then read off the result.

candle wax + water → stays separate
nonpolar solute · polar solvent · a mismatch: the wax needs a nonpolar solvent
Dr. Karmach

Where this goes wrong

Treating water as a universal solvent. Water dissolves many things, but only polar and ionic ones. A nonpolar solute like oil or grease is attracted to water far more weakly than water is to itself, so no amount of water dissolves it.
Arguing that opposite polarities attract. Opposite charges attract, plus to minus. Solubility does not work that way. It follows like dissolves like: a nonpolar solute needs a nonpolar solvent, never a polar one.
Expecting stirring to overcome a mismatch. Stirring and waiting change how fast a solute dissolves, never whether it dissolves. A polarity mismatch stays undissolved however long you stir.
Reading a big carbon molecule as automatically nonpolar. Sugar and glycerol are built on carbon, yet their many –OH groups are polar and hydrogen-bond with water. Count the polar groups before calling a molecule nonpolar.
Dr. Karmach

Practice 1

hexane, C₆H₁₄: a nonpolar solvent
candidates: table salt · glycerol · naphthalene (mothballs)

A chemist needs a solute that dissolves readily in hexane. Which candidate works best, and why?

  1. Table salt: an ionic solid, and ionic solids dissolve in almost any liquid
  2. Glycerol, C₃H₈O₃: built on carbon, so it counts as nonpolar
  3. Naphthalene, C₁₀H₈: a nonpolar solute, the same family as hexane
  4. Any of the three, as long as the mixture is stirred long enough
Dr. Karmach

Practice 1 answer: C

hexane (nonpolar) + naphthalene (nonpolar) → dissolves · answer C
same family · the other candidates are ionic or polar

A treats ionic solids as dissolving anywhere; ions need a polar solvent whose charged ends can surround them, and hexane has none. B judged glycerol by its carbon atoms; its three –OH groups make it polar, so it mixes with water, not hexane. D counts on stirring, which changes only the rate, never whether a mismatch dissolves.

Match the families first: nonpolar hexane takes the nonpolar naphthalene and leaves the salt and glycerol behind.
Dr. Karmach

Worked example 3: sugar in water

table sugar (C₁₂H₂₂O₁₁) stirred into water
carbon-heavy molecule · 342.30 g/mol · solvent: water, polar

Sugar is a large molecule built on a carbon framework, which makes it look nonpolar. Predict whether it dissolves in water, and why.

Dr. Karmach

Worked example 3: the polar groups

table sugar (C₁₂H₂₂O₁₁) stirred into water
carbon-heavy molecule · 342.30 g/mol · solvent: water, polar

Step 1 · Find the solute's polarity

The carbon framework is nonpolar, but the molecule carries eight polar –OH groups.

Dr. Karmach

Worked example 3: the polar groups

table sugar (C₁₂H₂₂O₁₁) stirred into water
carbon-heavy molecule · 342.30 g/mol · solvent: water, polar

Step 1 · Find the solute's polarity

The carbon framework is nonpolar, but the molecule carries eight polar –OH groups.

The carbon count is a distraction. The eight polar –OH groups decide it: sugar is polar.
Dr. Karmach

Worked example 3: the polar groups

table sugar (C₁₂H₂₂O₁₁) stirred into water
carbon-heavy molecule · 342.30 g/mol · solvent: water, polar

Step 1 · Find the solute's polarity

The carbon framework is nonpolar, but the molecule carries eight polar –OH groups.

The carbon count is a distraction. The eight polar –OH groups decide it: sugar is polar.
Step 2 · Find the solvent's polarity

Water is polar, and every one of those –OH groups can hydrogen-bond to it.

Dr. Karmach

Worked example 3: the match

table sugar (C₁₂H₂₂O₁₁): polar, covered in –OH groups
solvent: water, polar

Step 3 · Match them

polar solute · polar solvent → same family, it dissolves
Dr. Karmach

Worked example 3: the match

table sugar (C₁₂H₂₂O₁₁): polar, covered in –OH groups
solvent: water, polar

Step 3 · Match them

polar solute · polar solvent → same family, it dissolves
Do not judge a molecule by its carbon count. Sugar's eight polar –OH groups make it polar, so it dissolves in water. The tea turns sweet.
Dr. Karmach

Worked example 3: the route on the map

table sugar (C₁₂H₂₂O₁₁) stirred into water
eight –OH groups: polar solute · polar solvent · found: it dissolves

The –OH groups put sugar in the polar family with water, carbon framework and all. ✓
Dr. Karmach

Practice 2

copper(II) sulfate (CuSO₄) · erythritol (C₄H₁₀O₄, an –OH on every carbon) · β-carotene (C₄₀H₅₆)
the mixture is shaken with water and hexane, which settle into two layers

Where does each solute end up?

  1. All three in the water layer
  2. CuSO₄ in the water layer; erythritol and β-carotene in the hexane layer
  3. CuSO₄ and erythritol in the hexane layer; β-carotene in the water layer
  4. CuSO₄ and erythritol in the water layer; β-carotene in the hexane layer
Dr. Karmach

Practice 2 answer: D

water layer: CuSO₄ (ionic) and erythritol (polar) · hexane layer: β-carotene (nonpolar) · answer D
ionic and polar solutes with the polar solvent · nonpolar solute with the nonpolar solvent

CuSO₄ is ionic, so it belongs with polar water. Erythritol is built on carbon, but an –OH on every carbon makes it polar: water again. β-Carotene holds only C and H, so it is nonpolar: hexane.

A treated water as a universal solvent; it leaves nonpolar β-carotene out. B judged erythritol by its carbon skeleton instead of its –OH groups. C swapped the families, as if opposite polarities attract.

Sort each solute on its own: ionic or polar goes with water, nonpolar goes with hexane. Shaking changes only how fast they sort.
Dr. Karmach

Check yourself

  1. Iodine (I₂) is a nonpolar solid. It barely colors water but turns hexane deep purple. Which solvent dissolves it, and why?
  2. Rubbing alcohol mixes with water in any amount. What does that tell you about its polarity?

Some solutes keep dissolving in a solvent until the solvent can hold no more. That limit, and how temperature shifts it, is the next question about solutions.

Dr. Karmach

2 · Saturation & Solubility Curves

Read a solubility curve to find how much solute dissolves at a given temperature, classify a solution as unsaturated, saturated, or supersaturated, and find how much crystallizes when it cools.

Dr. Karmach

When sugar stops dissolving

Stir spoon after spoon of sugar into iced tea. At first it disappears. Past a point it just piles at the bottom, and warm tea takes far more.

Dr. Karmach

Every solute has a limit

solubility = the maximum solute that dissolves in a fixed amount of water at a given temperature
measured in grams of solute per 100 g of water, at a stated temperature
KNO₃ at 20 °C: 32 g per 100 g water
stir in more than 32 g and the extra cannot dissolve: it stays as solid

A fixed amount of water at a fixed temperature dissolves only so much solute. That ceiling, the solute's solubility, exists because dissolving and crystallizing reach a balance: particles return as fast as they leave.

Dr. Karmach

Unsaturated, saturated, supersaturated

Below the limit: unsaturated, more dissolves. At the limit: saturated, solid in balance with dissolved. Past it, after slow cooling with no seed crystal: supersaturated. One added crystal drops the excess out.

memory hook: UNDER · AT · OVER the limit
unsaturated · saturated · supersaturated ("super" = over)
Dr. Karmach

Reading the solubility curve

Warm water jostles the crystal apart faster than particles re-stick, so the KNO₃ curve climbs steeply while NaCl stays nearly flat. A warm gas molecule instead escapes the liquid more easily: gases dissolve less.

memory hook: hot tea takes more sugar · warm soda goes flat
most solids: more soluble when hot · gases: less soluble when hot
Dr. Karmach

The method

  1. Read the curve at the temperature. Grams per 100 g of water.
  2. Scale to the water present. × (grams of water ÷ 100).
  3. Compare with the limit. Below unsaturated, at saturated, above supersaturated. Cooling drops the excess out.
Dr. Karmach

Worked example 1: classifying a solution

100 g KNO₃ stirred into 200 g of water at 40 °C: it all dissolves
given: 100 g solute · 200 g water · 40 °C · wanted: unsaturated, saturated, or supersaturated?

A common first attempt: the curve reads 64 g at 40 °C, so 64 g is the most this beaker holds. Test it.

Classify the solution.

Dr. Karmach

Worked example 1: solution

100 g KNO₃ in 200 g of water at 40 °C
given: 100 g solute · 200 g water · 40 °C

A common first attempt

A first attempt uses 64 g as the limit. But 64 g is per 100 g of water, and this beaker holds 200 g. Scale it first.

Dr. Karmach

Worked example 1: solution

100 g KNO₃ in 200 g of water at 40 °C
given: 100 g solute · 200 g water · 40 °C
A common first attempt Step 1 · Read the curve at the temperature Step 2 · Scale to the water present

At 40 °C the KNO₃ curve reads 64 g per 100 g of water. Scale that to the 200 g in this beaker:

200 g H₂O × 64 g KNO₃100 g H₂O = 128 g KNO₃
Dr. Karmach

Worked example 1: solution

100 g KNO₃ in 200 g of water at 40 °C
given: 100 g solute · 200 g water · 40 °C
A common first attempt Step 1 · Read the curve at the temperature Step 2 · Scale to the water present
200 g H₂O × 64 g KNO₃100 g H₂O = 128 g KNO₃
Step 3 · Compare with the limit
128 g limit − 100 g present = 28 g of room left → unsaturated
Dr. Karmach

Worked example 1: solution

100 g KNO₃ in 200 g of water at 40 °C
given: 100 g solute · 200 g water · 40 °C
A common first attempt Step 1 · Read the curve at the temperature Step 2 · Scale to the water present
200 g H₂O × 64 g KNO₃100 g H₂O = 128 g KNO₃
Step 3 · Compare with the limit
128 g limit − 100 g present = 28 g of room left → unsaturated
The water could still take 28 g more KNO₃ before any solid appears. Below the limit means unsaturated.
Dr. Karmach

Worked example 1: the route on the map

100 g KNO₃ in 200 g of water at 40 °C
given: 100 g solute · 200 g water · 40 °C · found: limit 128 g · 28 g of room · unsaturated

Top lane only. Scaling doubles the 64 g reading, and 100 g sits below the 128 g limit. ✓
Dr. Karmach

Take-home: the curve value is per 100 g of water

curve read: 64 g per 100 g water at 40 °C
a ratio: the limit for this beaker depends on how much water it holds
200 g water → 200 g × (64 g / 100 g) = 128 g
scale before comparing: the beaker's limit is 128 g, not 64 g

Solubility is grams per 100 g of water. Multiply by the water actually present before judging saturation. Skipping the scale answers a different beaker.

Dr. Karmach

Worked example 2: cooling a saturated solution

100 g of water holds all the KNO₃ it can at 60 °C, then cools to 20 °C
given: 100 g water · saturated at 60 °C · cooled to 20 °C · wanted: grams that crystallize

A hot solution saturated with KNO₃ is left to cool on the bench.

How many grams of KNO₃ fall out as crystals?

Dr. Karmach

Worked example 2: solution

saturated KNO₃ in 100 g water · 60 °C → 20 °C
given: 100 g water · saturated at 60 °C · cooled to 20 °C

Step 1 · Read the curve at the temperature

at 60 °C = 106 g / 100 g water · at 20 °C = 32 g / 100 g water
Dr. Karmach

Worked example 2: solution

saturated KNO₃ in 100 g water · 60 °C → 20 °C
given: 100 g water · saturated at 60 °C · cooled to 20 °C
Step 1 · Read the curve at the temperature
at 60 °C = 106 g / 100 g water · at 20 °C = 32 g / 100 g water
Step 2 · Scale to the water present

The beaker holds 100 g of water, so the per-100-g values apply directly: 106 g dissolved at 60 °C, 32 g the limit at 20 °C.

Dr. Karmach

Worked example 2: solution

saturated KNO₃ in 100 g water · 60 °C → 20 °C
given: 100 g water · saturated at 60 °C · cooled to 20 °C
Step 1 · Read the curve at the temperature
at 60 °C = 106 g / 100 g water · at 20 °C = 32 g / 100 g water
Step 2 · Scale to the water present Step 3 · Compare with the limit
106 g dissolved − 32 g the cool water can hold = 74 g crystallize

At 60 °C all 106 g were dissolved. At 20 °C only 32 g can stay. The rest leaves solution as solid.

Dr. Karmach

Worked example 2: solution

saturated KNO₃ in 100 g water · 60 °C → 20 °C
given: 100 g water · saturated at 60 °C · cooled to 20 °C
Step 1 · Read the curve at the temperature
at 60 °C = 106 g / 100 g water · at 20 °C = 32 g / 100 g water
Step 2 · Scale to the water present Step 3 · Compare with the limit
106 g dissolved − 32 g the cool water can hold = 74 g crystallize
Cooling lowers the limit, and the 74 g it can no longer hold drops out as crystals. Less dissolves cold than hot.
Dr. Karmach

Worked example 2: the route on the map

saturated KNO₃ in 100 g water · 60 °C → 20 °C
given: 100 g water · saturated at 60 °C · cooled to 20 °C · found: 74 g crystallize

Saturated at the start, so the 60 °C limit is the grams dissolved. The 20 °C lane sets the new limit. ✓
Dr. Karmach

Your turn: cooling from 50 °C to 30 °C

saturated KNO₃ in 100 g of water at 50 °C, cooled to 30 °C
curve: 50 °C reads 85 g / 100 g water · 30 °C reads 46 g / 100 g water
85 g dissolved − 46 g the cool water can hold = g crystallize

Read both limits, then subtract to find what falls out.

Dr. Karmach

Your turn: cooling from 50 °C to 30 °C

saturated KNO₃ in 100 g of water at 50 °C, cooled to 30 °C
curve: 50 °C reads 85 g / 100 g water · 30 °C reads 46 g / 100 g water
85 g dissolved − 46 g the cool water can hold = g crystallize

Read both limits, then subtract to find what falls out.

85 g dissolved − 46 g the cool water can hold = 39 g crystallize

Cooling from 50 °C to 30 °C drops 39 g of KNO₃ out of solution.

Dr. Karmach

Where this goes wrong

Stirring past the limit. Add 90 g of a salt whose limit is 60 g, then stir for an hour: 60 g dissolves and 90 − 60 = 30 g stays on the bottom. Stirring speeds dissolving up to the limit; it cannot push past it.
Using the curve value without scaling. The curve gives grams per 100 g of water. For 150 g of water at 60 °C the beaker holds 150 × (106 g / 100 g) = 159 g, not 106 g. Scale to the water present first.
Adding instead of subtracting on cooling. A solution with 106 g dissolved, cooled to a 32 g limit, does not shed 106 + 32 = 138 g. What crystallizes is the excess: 106 − 32 = 74 g.
Reading at the wrong temperature. Cooling to 20 °C means reading the limit at 20 °C, not at 40 °C. The 40 °C value gives 106 − 64 = 42 g and understates the crystals. Read straight up from the final temperature.
Dr. Karmach

Practice 1

NaCl solubility at 20 °C: 36 g per 100 g of water
75 g of NaCl stirred into 50. g of water at 20 °C, stirred thoroughly

How many grams of NaCl remain undissolved at the bottom?

  1. 0
  2. 18
  3. 39
  4. 57
Dr. Karmach

Practice 1 answer: D

NaCl at 20 °C: 36 g per 100 g water · 75 g into 50. g water
scale the limit to 50. g of water, then subtract
50. g H₂O × 36 g NaCl100 g H₂O = 18 g dissolve
75 g added − 18 g dissolved = 57 g undissolved · answer D

A: 0 g assumes stirring dissolves everything; past the limit the extra stays solid. B: 18 g is how much dissolves, not what is left: 75 − 18 = 57. C: 39 g used 36 g as the limit for this beaker, but 36 g is per 100 g of water: only 50. g is here, so 50. × 36/100 = 18 g dissolves.

More salt was added than 50. g of water can hold, so solid must remain. The 18 g that dissolves leaves 57 g on the bottom. ✓
Dr. Karmach

Practice 2

KNO₃ curve: 136 g / 100 g water at 70 °C · 46.0 g / 100 g water at 30 °C
180. g of KNO₃ is dissolved in 250. g of water at 70 °C, then cooled to 30 °C

How many grams of KNO₃ crystallize?

  1. 225
  2. 115
  3. 65
  4. 134
Dr. Karmach

Practice 2 answer: C

180. g KNO₃ in 250. g water · cooled from 70 °C to 30 °C
scale both limits to 250. g of water
250. g H₂O × 136 g KNO₃100 g H₂O = 340. g limit at 70 °C · 180. g present: unsaturated
250. g H₂O × 46.0 g KNO₃100 g H₂O = 115 g stays · 180. − 115 = 65 g crystallize · answer C

A assumed a saturated start: 340. − 115 = 225 g, but only 180. g was dissolved. B stopped at 115 g, what stays dissolved. D used 46.0 g unscaled: 180. − 46.0 = 134 g.

Only what was dissolved can crystallize: 180. g in, 115 g stays, 65 g out. ✓
Dr. Karmach

Check yourself

  1. A solution holds 30 g of KNO₃ in 100 g of water at 60 °C, where the limit is 106 g. Unsaturated, saturated, or supersaturated?
  2. A solution saturated with KNO₃ at 40 °C (limit 64 g) in 100 g of water is cooled to 20 °C (limit 32 g). How many grams crystallize?

A dissolved solute raises the next question: how much of it is in the water: the concentration. Adding water lowers the concentration without changing the amount of solute, the relation M₁V₁ = M₂V₂.

Dr. Karmach

3 · Dilution

Use M₁V₁ = M₂V₂ to find a diluted concentration or the stock volume needed for a target, remembering that adding water conserves the moles of solute and that both volumes must share a unit.

Dr. Karmach

One can makes a whole pitcher

Frozen juice concentrate is thick and strong. Stir one small can into a pitcher of water and it becomes a full, mild drink. Same juice, just more liquid.

Dr. Karmach

The solute stays; only the water grows

Adding water spreads the solute through more liquid. Not one particle of solute is added or removed, so the moles of solute stay fixed. That conservation is the whole rule: M₁V₁ = M₂V₂.

Dr. Karmach

The four quantities in M₁V₁ = M₂V₂

Before diluting: concentration M₁ and volume V₁. After: concentration M₂ and volume V₂. Their products are equal because the moles of solute, concentration times volume, never change.

memory hook: 1 = before, 2 = after
M × V counts the moles of solute: the same number on both sides
Dr. Karmach

Both volumes in the same unit

M₁V₁ = M₂V₂
V₁ and V₂ both in mL, or both in L · the volume unit cancels across the equation

The relation balances only when V₁ and V₂ carry the same volume unit. Put both in milliliters or both in liters. The solved volume comes out in whatever unit you used.

Dr. Karmach

The method

  1. List the knowns: three of M₁, V₁, M₂, V₂; mark the unknown.
  2. Rearrange for the unknown in M₁V₁ = M₂V₂.
  3. Match the volume units: both mL, or both L.
  4. Substitute and solve; the diluted concentration comes out lower.
Dr. Karmach

Worked example 1: concentration after dilution

M₁V₁ = M₂V₂
given: 6.00 M · 25.0 mL stock · water to 150. mL final · wanted: M₂

A stockroom takes 25.0 mL of 6.00 M HCl and adds water to a final volume of 150. mL. Find the concentration of the diluted solution.

List the knowns, then rearrange M₁V₁ = M₂V₂ for M₂.

Dr. Karmach

Worked example 1: solution

M₁V₁ = M₂V₂
given: 6.00 M · 25.0 mL stock · water to 150. mL final · wanted: M₂

Step 1 · List the knowns

M₁ = 6.00 M. V₁ = 25.0 mL. V₂ = 150. mL. The unknown is M₂.

Dr. Karmach

Worked example 1: solution

M₁V₁ = M₂V₂
given: 6.00 M · 25.0 mL stock · water to 150. mL final · wanted: M₂
Step 1 · List the knowns Step 2 · Rearrange
M₁V₁ = M₂V₂ → M₂ = M₁ × V₁V₂
Dr. Karmach

Worked example 1: solution

M₁V₁ = M₂V₂
given: 6.00 M · 25.0 mL stock · water to 150. mL final · wanted: M₂
Step 1 · List the knowns Step 2 · Rearrange
M₁V₁ = M₂V₂ → M₂ = M₁ × V₁V₂
Step 3 · Match the units Step 4 · Substitute and solve

Both volumes are in mL, so the volume ratio cancels to a pure number.

M₂ = 6.00 M × 25.0 mL150. mL = 1.00 M
Dr. Karmach

Worked example 1: solution

M₁V₁ = M₂V₂
given: 6.00 M · 25.0 mL stock · water to 150. mL final · wanted: M₂
Step 1 · List the knowns Step 2 · Rearrange
M₁V₁ = M₂V₂ → M₂ = M₁ × V₁V₂
Step 3 · Match the units Step 4 · Substitute and solve
M₂ = 6.00 M × 25.0 mL150. mL = 1.00 M
The volume grew six-fold, from 25.0 to 150. mL, so the concentration falls six-fold: 6.00 ÷ 6 = 1.00 M. Diluting lowers the concentration ✓
Dr. Karmach

Worked example 1: the route on the map

M₁V₁ = M₂V₂
given: 6.00 M · 25.0 mL stock · 150. mL final · found: M₂ = 1.00 M

The unknown is the new concentration, so M₂ = M₁ × V₁ ÷ V₂. Both volumes are in mL, so their ratio is a pure number. ✓
Dr. Karmach

Worked example 2: final volume after dilution

M₁V₁ = M₂V₂
given: 6.00 M · 30.0 mL stock · dilute to 0.500 M · wanted: V₂

How much dilute solution results when 30.0 mL of 6.00 M NaOH is diluted with water to 0.500 M? Find the total volume.

A tempting setup puts the lower concentration on top. Weigh it against the sense check.

Dr. Karmach

Worked example 2: solution

M₁V₁ = M₂V₂
given: 6.00 M · 30.0 mL stock · dilute to 0.500 M · wanted: V₂

A common first attempt

V₂ = 30.0 mL × 0.500 M6.00 M = 2.50 mL ✗

A dilution that ends with less liquid than it started. The concentration ratio is upside down.

Dr. Karmach

Worked example 2: solution

M₁V₁ = M₂V₂
given: 6.00 M · 30.0 mL stock · dilute to 0.500 M · wanted: V₂
A common first attempt
V₂ = 30.0 mL × 0.500 M6.00 M = 2.50 mL ✗
Step 1 · List the knowns

M₁ = 6.00 M. V₁ = 30.0 mL. M₂ = 0.500 M. The unknown is V₂.

Dr. Karmach

Worked example 2: solution

M₁V₁ = M₂V₂
given: 6.00 M · 30.0 mL stock · dilute to 0.500 M · wanted: V₂
A common first attempt
V₂ = 30.0 mL × 0.500 M6.00 M = 2.50 mL ✗
Step 1 · List the knowns Step 2 · Rearrange

Solve M₁V₁ = M₂V₂ for V₂: it equals V₁ scaled by the concentration ratio M₁ ÷ M₂.

Dr. Karmach

Worked example 2: solution

M₁V₁ = M₂V₂
given: 6.00 M · 30.0 mL stock · dilute to 0.500 M · wanted: V₂
A common first attempt
V₂ = 30.0 mL × 0.500 M6.00 M = 2.50 mL ✗
Step 1 · List the knowns Step 2 · Rearrange Step 3 · Match the units Step 4 · Substitute and solve

V₁ is in mL, so V₂ comes out in mL. The starting concentration sits on top:

V₂ = 30.0 mL × 6.00 M0.500 M = 360 mL
Dr. Karmach

Worked example 2: solution

M₁V₁ = M₂V₂
given: 6.00 M · 30.0 mL stock · dilute to 0.500 M · wanted: V₂
A common first attempt
V₂ = 30.0 mL × 0.500 M6.00 M = 2.50 mL ✗
Step 1 · List the knowns Step 2 · Rearrange Step 3 · Match the units Step 4 · Substitute and solve
V₂ = 30.0 mL × 6.00 M0.500 M = 360 mL
6.00 M down to 0.500 M is a twelve-fold drop, so the volume grows: 30.0 mL × 12 = 360 mL ✓
Dr. Karmach

Worked example 2: the route on the map

M₁V₁ = M₂V₂
given: 6.00 M · 30.0 mL stock · dilute to 0.500 M · found: V₂ = 360 mL

The unknown is the final volume, so V₂ = V₁ × M₁ ÷ M₂. The question asked for the total volume, so the water step stays unlit. ✓
Dr. Karmach

Take-home: diluting grows the volume

V₂ = 30.0 mL × 0.500 M6.00 M = 2.50 mL ✗ · smaller than the start
V₂ = 30.0 mL × 6.00 M0.500 M = 360 mL ✓

Diluting spreads the solute through more liquid, so the final volume exceeds the start. Keep the higher starting concentration on top, and the volume grows. A shrinking result means the ratio was flipped.

Dr. Karmach

Your turn: glucose from a stock

M₁V₁ = M₂V₂
given: stock 1.50 M glucose · dilute to 0.300 M · final volume 250. mL · wanted: V₁

A recipe needs 250. mL of 0.300 M glucose, poured from a 1.50 M glucose stock. What volume of the stock delivers it?

V₁ = V₂ × M₂M₁ = mL × M M = mL

Fill the final volume, then the two concentrations, and compute the stock volume.

Dr. Karmach

Your turn: glucose from a stock

M₁V₁ = M₂V₂
given: stock 1.50 M glucose · dilute to 0.300 M · final volume 250. mL · wanted: V₁
V₁ = V₂ × M₂M₁ = mL × M M = mL
V₁ = V₂ × M₂M₁ = 250. mL × 0.300 M1.50 M = 50.0 mL
The stock is five times stronger, 1.50 M against 0.300 M, so it takes a fifth of the final volume: 250. ÷ 5 = 50.0 mL ✓
Dr. Karmach

Where this goes wrong

6.00 M · 30.0 mL stock · dilute to 0.500 M
correct: V₂ = 30.0 mL × (6.00 M ÷ 0.500 M) = 360 mL
Flipping the concentration ratio. 30.0 mL × (0.500 M ÷ 6.00 M) = 2.50 mL claims diluting shrank the liquid. The higher starting concentration goes on top: 30.0 × (6.00 ÷ 0.500) = 360 mL.
Stopping at the solute amount. 30.0 mL × 6.00 M = 180 gives the millimoles of solute, not a volume. Divide that by the new concentration: 180 ÷ 0.500 = 360 mL.
Reporting only the water added. 360 − 30.0 = 330 mL is the water poured in. The total volume still holds the original 30.0 mL of stock: 360 mL.
Dr. Karmach

Practice 1

M₁V₁ = M₂V₂
start 5.00 M HNO₃ · dilute to 0.400 M

You have 40.0 mL of 5.00 M nitric acid (HNO₃) and dilute it with water until the concentration is 0.400 M. What volume of water, in mL, must be added?

  1. 500.
  2. 460.
  3. 3.20
  4. 200.
Dr. Karmach

Practice 1 answer: B

M₁V₁ = M₂V₂
given: 5.00 M · 40.0 mL HNO₃ · dilute to 0.400 M · wanted: mL of water added
V₂ = 40.0 mL × 5.00 M0.400 M = 500. mL total → water = 500. − 40.0 = 460. mL · answer B

A stopped at the total volume: 500. mL still counts the 40.0 mL of acid already in the flask. C flipped the ratio: 40.0 × (0.400 ÷ 5.00) = 3.20 mL, less than the start. D stopped at the solute: 40.0 × 5.00 = 200. mmol of HNO₃, not a volume.

5.00 M down to 0.400 M is a 12.5-fold drop, so the solution grows to 500. mL; the acid supplied 40.0 mL of it and water the other 460. mL ✓
Dr. Karmach

Worked example 3: stock volume for a target

M₁V₁ = M₂V₂
given: dilute to 0.150 M · final volume 2.00 L · stock 6.00 M · wanted: mL of stock

A titration needs 2.00 L of 0.150 M HCl. The stockroom stocks 6.00 M HCl. What volume of the stock, in milliliters, do you measure out?

Track the unit on every volume as you go.

Dr. Karmach

Worked example 3: solution

M₁V₁ = M₂V₂
given: dilute to 0.150 M · final volume 2.00 L · stock 6.00 M · wanted: mL of stock

A common first attempt

V₁ = 2.00 L × 0.150 M6.00 M = 0.0500 mL ✗

A droplet cannot dilute to fill 2.00 L. The result came out in liters, because the volume entered in liters.

Dr. Karmach

Worked example 3: solution

M₁V₁ = M₂V₂
given: dilute to 0.150 M · final volume 2.00 L · stock 6.00 M · wanted: mL of stock
A common first attempt
V₁ = 2.00 L × 0.150 M6.00 M = 0.0500 mL ✗
Step 1 · List the knowns

M₂ = 0.150 M. V₂ = 2.00 L. M₁ = 6.00 M. The unknown is V₁, wanted in mL.

Dr. Karmach

Worked example 3: solution

M₁V₁ = M₂V₂
given: dilute to 0.150 M · final volume 2.00 L · stock 6.00 M · wanted: mL of stock
A common first attempt
V₁ = 2.00 L × 0.150 M6.00 M = 0.0500 mL ✗
Step 1 · List the knowns Step 2 · Rearrange

Solve M₁V₁ = M₂V₂ for V₁: it equals V₂ scaled by the concentration ratio M₂ ÷ M₁.

Dr. Karmach

Worked example 3: solution

M₁V₁ = M₂V₂
given: dilute to 0.150 M · final volume 2.00 L · stock 6.00 M · wanted: mL of stock
A common first attempt
V₁ = 2.00 L × 0.150 M6.00 M = 0.0500 mL ✗
Step 1 · List the knowns Step 2 · Rearrange Step 3 · Match the units Step 4 · Substitute and solve

V₂ entered in liters, so V₁ lands in liters. Convert to milliliters at the end:

V₁ = 2.00 L × 0.150 M6.00 M = 0.0500 L = 50.0 mL
Dr. Karmach

Worked example 3: solution

M₁V₁ = M₂V₂
given: dilute to 0.150 M · final volume 2.00 L · stock 6.00 M · wanted: mL of stock
A common first attempt
V₁ = 2.00 L × 0.150 M6.00 M = 0.0500 mL ✗
Step 1 · List the knowns Step 2 · Rearrange Step 3 · Match the units Step 4 · Substitute and solve
V₁ = 2.00 L × 0.150 M6.00 M = 0.0500 L = 50.0 mL
The stock is forty times stronger than 0.150 M, so V₁ is a fortieth of 2.00 L: 0.0500 L, 50.0 mL ✓
Dr. Karmach

Worked example 3: the route on the map

M₁V₁ = M₂V₂
given: 0.150 M · 2.00 L final · 6.00 M stock · found: V₁ = 50.0 mL

The unknown is the stock volume, so V₁ = V₂ × M₂ ÷ M₁. The new move is the unit: V₂ in liters, the answer wanted in mL. ✓
Dr. Karmach

Practice 2

M₁V₁ = M₂V₂
stock 4.50 M KOH · target 0.400 M · final volume 0.900 L

A lab needs 0.900 L of 0.400 M KOH, made from a 4.50 M KOH stock. How many milliliters of water are added to the measured stock?

  1. 80.0
  2. 0.360
  3. 820.
  4. 0.820
Dr. Karmach

Practice 2 answer: C

M₁V₁ = M₂V₂
given: 0.400 M · 0.900 L final · stock 4.50 M · wanted: mL of water added
V₁ = 0.900 L × 0.400 M4.50 M = 0.0800 L = 80.0 mL of stock
water = 900. mL − 80.0 mL = 820. mL · answer C

A stopped at the stock: 80.0 mL is what gets measured, and water fills the rest. B stopped at the solute: 0.900 × 0.400 = 0.360 mol of KOH, not a volume. D subtracted in liters: 0.900 − 0.0800 = 0.820 L, not mL; convert both volumes first.

The stock is 11.25 times stronger than the target, so it fills only a small share of the 900. mL; water fills the other 820. mL ✓
Dr. Karmach

Check yourself

  1. A bottle reads 6.00 M NaOH. Write M₁V₁ = M₂V₂ for making 250. mL of 0.300 M NaOH, with the three known values filled in. Which volume is larger: the stock you measure, or 250. mL?
  2. You dilute a stock and your result for the final volume comes out smaller than the volume you started with. Name the error, and state which concentration belongs on top of the ratio.

Molarity reports solute per liter of solution. The same amount can be reported per kilogram of solvent (molality), or as a percent by mass or by volume. Diluting still conserves the solute; only the per-amount unit changes.

Dr. Karmach

4 · Molality & Mole Fraction

Calculate the molality of a solution from grams of solute and grams of solvent, find the mole fraction of each component, and explain why these measures do not change with temperature.

Dr. Karmach

Coolant that warms and swells

Antifreeze in a cold engine sits at a low line. Running hot, the same liquid expands and rises. Its blend never changed: only the space it fills.

Dr. Karmach

Measured by amount and mass, not volume

Molarity divides by the solution's volume, and volume swells when warmed. Molality and mole fraction count moles and weigh mass, so temperature does not change them.

Dr. Karmach

Molality: moles of solute per kilogram of solvent

m = mol solute ÷ kg solvent
a 2.0 m solution: every kilogram of the SOLVENT carries 2.0 mol solute · read "two molal"

Molality, symbol m, counts the moles of solute in each kilogram of solvent. The denominator is the solvent alone: not the solution, and not a volume.

memory hook: little m, mass of solvent · big M, liters of solution
m = mol ÷ kg solvent · M = mol ÷ L solution
Dr. Karmach

Temperature changes volume, not mass

warm a solution: volume 1.00 L → 1.03 L · molarity falls
the moles are unchanged, but they now spread through more liters
warm the same solution: solvent mass 1.00 kg → 1.00 kg · molality holds
mass does not expand, so moles per kilogram stay put

Heat expands a liquid's volume but never its mass. Molarity changes with temperature; molality and mole fraction do not.

Dr. Karmach

Mole fraction: a component's share of the moles

The mole fraction X of a component is its moles divided by the total moles. It carries no units, and the fractions of all components add to 1.

Dr. Karmach

The method

  1. Grams → moles: convert the solute's mass with its molar mass.
  2. Grams → kilograms: divide the solvent's mass by 1000.
  3. Divide moles by kilograms: the quotient is the molality, in mol/kg.

Backward: kilograms × molality → moles → grams.

Dr. Karmach

Worked example 1: molality from grams

m = mol solute ÷ kg solvent
given: 18.0 g glucose (C₆H₁₂O₆, 180.16 g/mol) · 250. g water · wanted: m

A syrup is made by dissolving 18.0 g of glucose (C₆H₁₂O₆, 180.16 g/mol) in 250. g of water. Find the molality.

Set it up: turn the solute into moles and the solvent into kilograms, then divide.

Dr. Karmach

Worked example 1: solution

m = mol solute ÷ kg solvent
given: 18.0 g glucose (180.16 g/mol) · 250. g water · wanted: m

Step 1 · Grams → moles

The molar mass converts the solute's mass to moles: 18.0 g ÷ 180.16 g/mol = 0.0999 mol glucose.

Dr. Karmach

Worked example 1: solution

m = mol solute ÷ kg solvent
given: 18.0 g glucose (180.16 g/mol) · 250. g water · wanted: m
Step 1 · Grams → moles Step 2 · Grams → kilograms
250. g water = 0.250 kg water
1000 g = 1 kg · molality counts kilograms of the solvent
Dr. Karmach

Worked example 1: solution

m = mol solute ÷ kg solvent
given: 18.0 g glucose (180.16 g/mol) · 250. g water · wanted: m
Step 1 · Grams → moles Step 2 · Grams → kilograms
250. g water = 0.250 kg water
1000 g = 1 kg · molality counts kilograms of the solvent
Step 3 · Divide moles by kilograms
m = 0.0999 mol glucose0.250 kg water = 0.400 mol/kg
Dr. Karmach

Worked example 1: solution

m = mol solute ÷ kg solvent
given: 18.0 g glucose (180.16 g/mol) · 250. g water · wanted: m
Step 1 · Grams → moles Step 2 · Grams → kilograms
250. g water = 0.250 kg water
1000 g = 1 kg · molality counts kilograms of the solvent
Step 3 · Divide moles by kilograms
m = 0.0999 mol glucose0.250 kg water = 0.400 mol/kg
A quarter kilogram of water carries 0.0999 mol, so a full kilogram carries four times that: 0.400 mol. 0.400 m ✓
Dr. Karmach

Worked example 1: the route on the map

m = mol solute ÷ kg solvent
given: 18.0 g glucose (180.16 g/mol) · 250. g water · found: 0.400 mol/kg

Three moves: each mass converts on its own side, then moles ÷ kilograms. ✓
Dr. Karmach

Worked example 2: mole fraction in antifreeze

X = mol of one component ÷ total mol
given: 62.0 g ethylene glycol (C₂H₆O₂, 62.07 g/mol) · 180. g water (18.02 g/mol) · wanted: X of each

An antifreeze mix contains 62.0 g of ethylene glycol (62.07 g/mol) and 180. g of water (18.02 g/mol). Find the mole fraction of each component.

Set it up: both masses become moles before any fraction is taken.

Dr. Karmach

Worked example 2: solution

X = mol of one component ÷ total mol
given: 62.0 g ethylene glycol (62.07 g/mol) · 180. g water (18.02 g/mol) · wanted: X of each

Grams → moles, each component

Ethylene glycol: 62.0 g ÷ 62.07 g/mol = 0.999 mol. Water: 180. g ÷ 18.02 g/mol = 9.99 mol.

Dr. Karmach

Worked example 2: solution

X = mol of one component ÷ total mol
given: 62.0 g ethylene glycol (62.07 g/mol) · 180. g water (18.02 g/mol) · wanted: X of each
Grams → moles, each component Divide each by the total moles
Xglycol = 0.999 mol(0.999 + 9.99) mol = 0.0909
Xwater = 9.99 mol10.99 mol = 0.909
Dr. Karmach

Worked example 2: solution

X = mol of one component ÷ total mol
given: 62.0 g ethylene glycol (62.07 g/mol) · 180. g water (18.02 g/mol) · wanted: X of each
Grams → moles, each component Divide each by the total moles
Xglycol = 0.999 mol(0.999 + 9.99) mol = 0.0909
Xwater = 9.99 mol10.99 mol = 0.909
The two fractions add to 1.000, and water, the greater amount, takes the larger share. 0.0909 + 0.909 = 1.000 ✓
Dr. Karmach

Your turn: sucrose in water

m = mol solute ÷ kg solvent
given: 34.2 g sucrose (C₁₂H₂₂O₁₁, 342.30 g/mol) · 500. g water · wanted: m

A sweetened solution holds 34.2 g of sucrose (342.30 g/mol) in 500. g of water.

34.2 g sucrose × 1 mol sucrose g sucrose = mol, then mol sucrose kg water = mol/kg

Fill the molar mass, the moles, and the kilograms of solvent, then compute the molality.

Dr. Karmach

Your turn: sucrose in water

m = mol solute ÷ kg solvent
given: 34.2 g sucrose (C₁₂H₂₂O₁₁, 342.30 g/mol) · 500. g water · wanted: m

A sweetened solution holds 34.2 g of sucrose (342.30 g/mol) in 500. g of water.

34.2 g sucrose × 1 mol sucrose g sucrose = mol, then mol sucrose kg water = mol/kg

Fill the molar mass, the moles, and the kilograms of solvent, then compute the molality.

34.2 g sucrose × 1 mol sucrose342.30 g sucrose = 0.0999 mol, then 0.0999 mol sucrose0.500 kg water = 0.200 mol/kg
Dr. Karmach

Where this goes wrong

18.0 g glucose (180.16 g/mol) · 250. g water
correct: 18.0 g → 0.0999 mol · 250. g → 0.250 kg · m = 0.400 mol/kg
Dividing by grams of solvent. 0.0999 mol ÷ 250 g = 0.000400, and the unit is mol/g, 1000 times too small. Molality divides by kilograms: 0.0999 ÷ 0.250 = 0.400 mol/kg.
Using the mass of the solution. The whole solution is 250 + 18.0 = 268 g, or 0.268 kg, giving 0.0999 ÷ 0.268 = 0.373. Molality uses the solvent alone: 0.250 kg.
Skipping the molar mass. 18.0 g ÷ 0.250 kg = 72.0 treats grams as moles. Grams become moles first: 18.0 ÷ 180.16 = 0.0999 mol.
Dividing by the solvent's moles alone. For 0.999 mol glycol and 9.99 mol water, 0.999 ÷ 9.99 = 0.100. A mole fraction divides by the TOTAL: 0.999 ÷ 10.99 = 0.0909.
Dr. Karmach

Practice 1

X = mol of one component ÷ total mol
molar masses: ethanol (C₂H₅OH) 46.07 g/mol · water 18.02 g/mol

A mix holds 23.0 g of ethanol and 54.0 g of water. What is the mole fraction of ethanol?

  1. 0.143
  2. 0.167
  3. 0.299
  4. 0.499
Dr. Karmach

Practice 1 answer: A

X = mol of one component ÷ total mol
given: 23.0 g ethanol (46.07 g/mol) · 54.0 g water (18.02 g/mol) · wanted: Xethanol
23.0 g ÷ 46.07 g/mol = 0.499 mol ethanol · 54.0 g ÷ 18.02 g/mol = 3.00 mol water
Xethanol = 0.499 mol(0.499 + 3.00) mol = 0.143 · answer A

B divided by the water's moles alone: 0.499 ÷ 3.00 = 0.167. C skipped the molar masses: 23.0 ÷ 77.0 = 0.299 is a mass fraction. D stopped at 0.499 mol ethanol, before dividing by the total.

Water outnumbers ethanol six to one in moles, so ethanol holds about a seventh of the total: 0.143 ✓
Dr. Karmach

Worked example 3: grams of solute for a target molality

m = mol solute ÷ kg solvent
given: 3.00 m urea (CH₄N₂O, 60.06 g/mol) · 250. g water · wanted: g urea

A fertilizer solution must be 3.00 m urea, made with 250. g of water. What mass of urea dissolves?

A common first attempt keeps the water in grams. Test the size of the answer.

Dr. Karmach

Worked example 3: solution

m = mol solute ÷ kg solvent
given: 3.00 m urea (60.06 g/mol) · 250. g water · wanted: g urea

A common first attempt

250 g water × 3.00 mol urea1 kg water × 60.06 g urea1 mol urea = 4.50 × 10⁴ g ✗

Forty-five kilograms of urea in a cup of water. The grams of water never cancel the kilograms in the molality.

Dr. Karmach

Worked example 3: solution

m = mol solute ÷ kg solvent
given: 3.00 m urea (60.06 g/mol) · 250. g water · wanted: g urea
A common first attempt
250 g water × 3.00 mol urea1 kg water × 60.06 g urea1 mol urea = 4.50 × 10⁴ g ✗
Backward · kilograms

The molality counts per kilogram of solvent: 250. g water = 0.250 kg water.

Dr. Karmach

Worked example 3: solution

m = mol solute ÷ kg solvent
given: 3.00 m urea (60.06 g/mol) · 250. g water · wanted: g urea
A common first attempt
250 g water × 3.00 mol urea1 kg water × 60.06 g urea1 mol urea = 4.50 × 10⁴ g ✗
Backward · kilograms Backward · molality → moles → grams
0.250 kg water × 3.00 mol urea1 kg water × 60.06 g urea1 mol urea = 45.0 g urea
Dr. Karmach

Worked example 3: solution

m = mol solute ÷ kg solvent
given: 3.00 m urea (60.06 g/mol) · 250. g water · wanted: g urea
A common first attempt
250 g water × 3.00 mol urea1 kg water × 60.06 g urea1 mol urea = 4.50 × 10⁴ g ✗
Backward · kilograms Backward · molality → moles → grams
0.250 kg water × 3.00 mol urea1 kg water × 60.06 g urea1 mol urea = 45.0 g urea
A quarter kilogram of water takes a quarter of 3.00 mol: 0.750 mol, and 0.750 mol × 60.06 g/mol = 45.0 g ✓
Dr. Karmach

Worked example 3: the route on the map

m = mol solute ÷ kg solvent
given: 3.00 m urea (60.06 g/mol) · 250. g water · found: 45.0 g urea

Worked example 1's route, run backward: the water enters in kilograms, the molality carries it across to moles, and the molar mass turns moles into grams. ✓
Dr. Karmach

Take-home: the solvent enters in kilograms

250 g water × 3.00 mol1 kg water × 60.06 g1 mol = 4.50 × 10⁴ g ✗ · g and kg never cancel
0.250 kg water × 3.00 mol1 kg water × 60.06 g1 mol = 45.0 g ✓

Molality is defined per kilogram of solvent. Solvent left in grams puts the answer off by 1000. Convert grams to kilograms, and use the solvent, never the solution.

Dr. Karmach

Practice 2

windshield-washer fluid: 2.00 m methanol (CH₃OH) in water
molar mass water 18.02 g/mol

A washer fluid is labeled 2.00 m methanol. Find the methanol's mole fraction.

  1. 0.00200
  2. 0.0360
  3. 55.5
  4. 0.0348
  5. 0.965
Dr. Karmach

Practice 2 answer: D

2.00 m methanol: 2.00 mol methanol = 1 kg water
basis: 1 kg (1000 g) of water · 18.02 g/mol · wanted: Xmethanol
1000 g water × 1 mol water18.02 g water = 55.5 mol water
Xmethanol = 2.00 mol(2.00 + 55.5) mol = 0.0348 · answer D

A kept the water in grams: 2.00 ÷ 1002 = 0.00200. B divided by the water alone: 2.00 ÷ 55.5 = 0.0360. C stopped at the water's moles. E is the water's share: 55.5 ÷ 57.5 = 0.965.

Methanol's molar mass never entered: the molality already counts its moles. ✓
Dr. Karmach

Check yourself

  1. A solution is prepared from grams of solute and grams of water. Which mass belongs in the denominator of molality, the solvent's or the whole solution's, and in what unit?
  2. A two-component mixture has X = 0.30 for one component. What is the mole fraction of the other?

Molarity counts moles per liter of solution; molality counts moles per kilogram of solvent. Given the solution's density, either concentration can be converted into the other.

Dr. Karmach

5 · Converting Concentration Units

Convert a solution's concentration among mass percent, molarity, and molality by taking a convenient basis and bridging with density and molar mass.

Dr. Karmach

The label reads 37%. The lab wants moles.

A jug of hydrochloric acid is labeled 37% by mass. The experiment needs it in moles per liter. The density on the label connects the two.

Dr. Karmach

Concentration labels are conversion factors

A concentration is a ratio: solute per amount of solution or solvent. Any ratio works as a conversion factor. Density, mass percent, and molar mass are all familiar. Chained, their units cancel one after another.

mL soln × g solnmL soln × g soluteg soln × mol soluteg solute = mol solute
density (g/mL) · mass percent (g per 100 g) · molar mass (g/mol)
each is a ratio of two amounts · each cancels one unit and brings in the next
Dr. Karmach

One solution, three descriptions

The same bottle can be reported three ways: mass percent, molality, or molarity. Each counts the solute against a different amount. Density and molar mass carry one description into another.

memory hook: M per L solution · m per kg solvent · % per 100 g solution
three denominators, one solute · solvent = solution − solute
Dr. Karmach

Density and molar mass convert the units

1 mL of solution = (density) grams · 1 mol of solute = (molar mass) grams
density crosses volume ↔ mass · molar mass crosses mass ↔ moles

Mass percent and molality describe the solute per unit mass; molarity describes it per unit volume. Density carries a mass to a volume; molar mass carries a mass to a mole count.

Dr. Karmach

Pick a convenient basis

Concentration is a rate: the same for a drop or a drum. Take whatever amount makes the numbers easy: 1 L for molarity, 100 g for mass percent or molality. The ratio is the same.

Dr. Karmach

The method

  1. Pick a basis: 1 L, or the batch.
  2. Density links volume and mass: mL × density = g; g ÷ density = mL.
  3. Find the solute: grams, moles.
  4. Divide by the asked amount: L solution, g solution, kg solvent.

Dr. Karmach

Worked example 1: mass percent to molarity

37.0% (m/m) HCl · density 1.19 g/mL · molar mass 36.46 g/mol
given: the label · wanted: molarity · basis: take 1 L of solution

Concentrated hydrochloric acid is 37.0% by mass, with a density of 1.19 g/mL. What is its molarity?

Take 1 L, then convert with the density and the molar mass.

Dr. Karmach

Worked example 1: solution

37.0% (m/m) HCl · density 1.19 g/mL · molar mass 36.46 g/mol

Three conversion factors carry 1 L of solution to moles of HCl.

Step 1 · Pick a basis

Take exactly 1 L (1000 mL) of the solution.

Dr. Karmach

Worked example 1: solution

37.0% (m/m) HCl · density 1.19 g/mL · molar mass 36.46 g/mol
Step 1 · Pick a basis Step 2 · Density links volume and mass

The density weighs that liter: 1000 mL × 1.19 g/mL = 1190 g of solution.

Dr. Karmach

Worked example 1: solution

37.0% (m/m) HCl · density 1.19 g/mL · molar mass 36.46 g/mol
Step 1 · Pick a basis Step 2 · Density links volume and mass Step 3 · Find the solute

The label makes 37.0% of that mass HCl: 0.370 × 1190 g = 440.3 g HCl. The molar mass turns it into moles:

1000 mL soln × 1.19 g soln1 mL soln × 37.0 g HCl100 g soln × 1 mol HCl36.46 g HCl = 12.1 mol HCl
Dr. Karmach

Worked example 1: solution

37.0% (m/m) HCl · density 1.19 g/mL · molar mass 36.46 g/mol
Step 1 · Pick a basis Step 2 · Density links volume and mass Step 3 · Find the solute
1000 mL soln × 1.19 g soln1 mL soln × 37.0 g HCl100 g soln × 1 mol HCl36.46 g HCl = 12.1 mol HCl
Step 4 · Divide by the asked amount
M = 12.1 mol HCl1 L solution = 12.1 M
Dr. Karmach

Worked example 1: solution

37.0% (m/m) HCl · density 1.19 g/mL · molar mass 36.46 g/mol
Step 1 · Pick a basis Step 2 · Density links volume and mass Step 3 · Find the solute
1000 mL soln × 1.19 g soln1 mL soln × 37.0 g HCl100 g soln × 1 mol HCl36.46 g HCl = 12.1 mol HCl
Step 4 · Divide by the asked amount
M = 12.1 mol HCl1 L solution = 12.1 M
12.1 mol fill the 1 L chosen: 12.1 M. The liter weighs 1190 g, over a third of it HCl. ✓

Dr. Karmach

Worked example 2: concentrated sulfuric acid

98.0% (m/m) H₂SO₄ · density 1.84 g/mL · molar mass 98.08 g/mol
given: the label · wanted: molarity · basis: take 1 L of solution

Concentrated sulfuric acid is 98.0% by mass, with a density of 1.84 g/mL. What is its molarity?

A common first attempt reads 1 L as 1000 g of solution. Test that against the density.

Dr. Karmach

Worked example 2: solution

98.0% (m/m) H₂SO₄ · density 1.84 g/mL · molar mass 98.08 g/mol

Step 1 · Pick a basis

Take 1 L (1000 mL) of the concentrated acid.

Dr. Karmach

Worked example 2: solution

98.0% (m/m) H₂SO₄ · density 1.84 g/mL · molar mass 98.08 g/mol
Step 1 · Pick a basis A common first attempt
1000 g soln × 98.0 g H₂SO₄100 g soln × 1 mol H₂SO₄98.08 g H₂SO₄ = 9.99 M ✗

That treated 1 L as 1000 g. This acid is far denser than water.

Dr. Karmach

Worked example 2: solution

98.0% (m/m) H₂SO₄ · density 1.84 g/mL · molar mass 98.08 g/mol
Step 1 · Pick a basis A common first attempt
1000 g soln × 98.0 g H₂SO₄100 g soln × 1 mol H₂SO₄98.08 g H₂SO₄ = 9.99 M ✗
Step 2 · Density links volume and mass

At 1.84 g/mL the liter weighs 1000 mL × 1.84 = 1840 g, not 1000 g.

Dr. Karmach

Worked example 2: solution

98.0% (m/m) H₂SO₄ · density 1.84 g/mL · molar mass 98.08 g/mol
Step 1 · Pick a basis A common first attempt
1000 g soln × 98.0 g H₂SO₄100 g soln × 1 mol H₂SO₄98.08 g H₂SO₄ = 9.99 M ✗
Step 2 · Density links volume and mass Step 3 · Find the solute Step 4 · Divide by the asked amount
1000 mL soln × 1.84 g soln1 mL soln × 98.0 g H₂SO₄100 g soln × 1 mol H₂SO₄98.08 g H₂SO₄ = 18.4 mol H₂SO₄
Dr. Karmach

Worked example 2: solution

98.0% (m/m) H₂SO₄ · density 1.84 g/mL · molar mass 98.08 g/mol
Step 1 · Pick a basis A common first attempt
1000 g soln × 98.0 g H₂SO₄100 g soln × 1 mol H₂SO₄98.08 g H₂SO₄ = 9.99 M ✗
Step 2 · Density links volume and mass Step 3 · Find the solute Step 4 · Divide by the asked amount
1000 mL soln × 1.84 g soln1 mL soln × 98.0 g H₂SO₄100 g soln × 1 mol H₂SO₄98.08 g H₂SO₄ = 18.4 mol H₂SO₄
18.4 mol in 1 L: 18.4 M. Skipping the density gave 9.99 M; the liter weighs 1840 g, not 1000. ✓

Dr. Karmach

Take-home: weigh the liter with the density

1000 g soln × 98.0 g H₂SO₄100 g soln × 1 mol98.08 g H₂SO₄ = 9.99 M ✗ · 1 L read as 1000 g
1000 mL soln × 1.84 g soln1 mL soln × 98.0 g H₂SO₄100 g soln × 1 mol98.08 g H₂SO₄ = 18.4 M ✓

The density sets the mass of a liter of solution. Skip it and every molarity comes out too low. Weigh the liter first, then take the solute's share.

Dr. Karmach

Your turn: nitric acid

30.0% (m/m) HNO₃ · density 1.18 g/mL · molar mass 63.01 g/mol
basis: take 1 L of solution · wanted: molarity

A cleaning-grade nitric acid is 30.0% by mass, density 1.18 g/mL.

1000 mL soln × g soln1 mL soln × 30.0 g HNO₃100 g soln × 1 mol HNO₃ g HNO₃ = M

Fill the density, the molar mass, and the molarity, then compute.

Dr. Karmach

Your turn: nitric acid

30.0% (m/m) HNO₃ · density 1.18 g/mL · molar mass 63.01 g/mol
basis: take 1 L of solution · wanted: molarity

A cleaning-grade nitric acid is 30.0% by mass, density 1.18 g/mL.

1000 mL soln × g soln1 mL soln × 30.0 g HNO₃100 g soln × 1 mol HNO₃ g HNO₃ = M

Fill the density, the molar mass, and the molarity, then compute.

1000 mL soln × 1.18 g soln1 mL soln × 30.0 g HNO₃100 g soln × 1 mol HNO₃63.01 g HNO₃ = 5.62 M

Dr. Karmach

Where this goes wrong

37.0% (m/m) HCl · density 1.19 g/mL · molar mass 36.46 g/mol
correct: 1 L → 1190 g → 440.3 g HCl → 12.1 mol → 12.1 M
Skipping the density. Reading 1 L as 1000 g: 0.370 × 1000 ÷ 36.46 = 10.1 M. But a liter of this acid weighs 1000 × 1.19 = 1190 g, not 1000. With the density: 12.1 M.
Dividing by the density. 0.370 × 1000 ÷ 1.19 ÷ 36.46 = 8.53 M. Mass is volume × density, so the milliliters multiply by 1.19. Multiplying gives 1190 g and 12.1 M.
Dropping the 1000 mL in a liter. 0.370 × 1.19 ÷ 36.46 = 0.0121: a thousand times too small. A liter is 1000 mL, so 1 L weighs 1190 g and the molarity is 12.1 M.
Dr. Karmach

Practice 1

15.0% (m/m) NaOH · density 1.16 g/mL · molar mass 40.00 g/mol
basis: take 1 L of solution · wanted: molarity

A stock 15.0% (m/m) sodium hydroxide solution has a density of 1.16 g/mL. What is its molarity?

  1. 4.35
  2. 3.23
  3. 3.75
  4. 0.00435
Dr. Karmach

Practice 1 answer: A

15.0% (m/m) NaOH · density 1.16 g/mL · molar mass 40.00 g/mol
basis: take 1 L → 1160 g solution · wanted: molarity
1000 mL soln × 1.16 g soln1 mL soln × 15.0 g NaOH100 g soln × 1 mol NaOH40.00 g NaOH = 4.35 M · answer A

C skipped the density: 0.150 × 1000 ÷ 40.00 = 3.75, reading 1 L as 1000 g instead of 1160 g. B divided by the density: 0.150 × 1000 ÷ 1.16 ÷ 40.00 = 3.23. D dropped the 1000 mL: 0.150 × 1.16 ÷ 40.00 = 0.00435, a thousand times too small.

A liter weighs 1160 g, 174 g of it NaOH, and 174 g ÷ 40.00 g/mol = 4.35 mol: 4.35 M. ✓

Dr. Karmach

Worked example 3: molarity to mass percent and molality

Step 1 · Pick a basis

4.50 M H₂SO₄ · density 1.25 g/mL · molar mass 98.08 g/mol
given: molarity and density · wanted: mass percent, then molality · basis: take 1 L of solution

Battery acid is 4.50 M sulfuric acid with a density of 1.25 g/mL. What are its mass percent and its molality?

The same liter answers both. Only the denominator changes.

Dr. Karmach

Worked example 3: mass percent

4.50 M H₂SO₄ · density 1.25 g/mL · molar mass 98.08 g/mol

Step 2 · Density links volume and mass

1000 mL soln × 1.25 g soln1 mL soln = 1250 g solution
Dr. Karmach

Worked example 3: mass percent

4.50 M H₂SO₄ · density 1.25 g/mL · molar mass 98.08 g/mol
Step 2 · Density links volume and mass
1000 mL soln × 1.25 g soln1 mL soln = 1250 g solution
Step 3 · Find the solute

The molarity puts 4.50 mol in the liter, and the molar mass weighs them: 4.50 mol × 98.08 g/mol = 441.4 g H₂SO₄.

Dr. Karmach

Worked example 3: mass percent

4.50 M H₂SO₄ · density 1.25 g/mL · molar mass 98.08 g/mol
Step 2 · Density links volume and mass
1000 mL soln × 1.25 g soln1 mL soln = 1250 g solution
Step 3 · Find the solute Step 4 · Divide by the asked amount
441.4 g H₂SO₄1250 g solution × 100 = 35.3% (m/m)
Dr. Karmach

Worked example 3: mass percent

4.50 M H₂SO₄ · density 1.25 g/mL · molar mass 98.08 g/mol
Step 2 · Density links volume and mass
1000 mL soln × 1.25 g soln1 mL soln = 1250 g solution
Step 3 · Find the solute Step 4 · Divide by the asked amount
441.4 g H₂SO₄1250 g solution × 100 = 35.3% (m/m)
The liter weighs 1250 g and carries 441 g of acid, a bit over a third: 35.3%. ✓

Dr. Karmach

Worked example 3: molality

1 L of 4.50 M H₂SO₄ = 1250 g solution, 441.4 g of it H₂SO₄

A common first attempt

m = 4.50 mol H₂SO₄1.250 kg solution = 3.60 mol/kg ✗

That kilogram count includes the acid. Molality divides by the solvent alone.

Dr. Karmach

Worked example 3: molality

1 L of 4.50 M H₂SO₄ = 1250 g solution, 441.4 g of it H₂SO₄
A common first attempt
m = 4.50 mol H₂SO₄1.250 kg solution = 3.60 mol/kg ✗
Step 4 · Divide by the asked amount

The water is what remains: 1250 g − 441.4 g = 808.6 g = 0.809 kg.

m = 4.50 mol H₂SO₄0.809 kg water = 5.56 mol/kg
Dr. Karmach

Worked example 3: molality

1 L of 4.50 M H₂SO₄ = 1250 g solution, 441.4 g of it H₂SO₄
A common first attempt
m = 4.50 mol H₂SO₄1.250 kg solution = 3.60 mol/kg ✗
Step 4 · Divide by the asked amount
m = 4.50 mol H₂SO₄0.809 kg water = 5.56 mol/kg
Under a kilogram of water carries the 4.50 mol, so 5.56 m runs above 4.50 M. ✓

Dr. Karmach

Practice 2

4.00 M NaCl · density 1.15 g/mL · molar mass 58.44 g/mol
basis: take 1 L of solution · wanted: mass percent

A road-deicing brine is 4.00 M sodium chloride with a density of 1.15 g/mL. What is its mass percent?

  1. 23.4
  2. 26.9
  3. 234
  4. 20.3
Dr. Karmach

Practice 2 answer: D

4.00 M NaCl · density 1.15 g/mL · molar mass 58.44 g/mol
4.00 mol × 58.44 g/mol = 233.8 g NaCl · 1000 mL soln × 1.15 g soln1 mL soln = 1150 g soln
233.8 g NaCl1150 g soln × 100 = 20.3% (m/m) · answer D

A skipped the density: 233.8 ÷ 1000 × 100 = 23.4. B divided by it: 1000 ÷ 1.15 = 870 g, 233.8 ÷ 870 × 100 = 26.9. C stopped at 234 g of NaCl, a mass, not a percent.

The liter weighs 1150 g and carries 234 g of salt, about a fifth: 20.3%. ✓

Dr. Karmach

Guided example: a solution mixed by mass

18.0 g KNO₃ + 132 g water · density 1.08 g/mL · molar mass 101.11 g/mol
given: the recipe and the density · wanted: molarity · basis: the batch as mixed

A fertilizer solution is made by dissolving 18.0 g of potassium nitrate in 132 g of water. The solution's density is 1.08 g/mL. What is its molarity?

Work all four steps of the method.

Dr. Karmach

Guided example: solution

18.0 g KNO₃ + 132 g water · density 1.08 g/mL · molar mass 101.11 g/mol

Two conversion factors are needed: the density and the molar mass.

Step 1 · Pick a basis

Take the batch as mixed. The solution is solute plus water: 18.0 g + 132 g = 150. g of solution.

Dr. Karmach

Guided example: solution

18.0 g KNO₃ + 132 g water · density 1.08 g/mL · molar mass 101.11 g/mol
Step 1 · Pick a basis Step 2 · Density links volume and mass

Molarity needs liters. The density turns grams of solution into milliliters:

18.0 g + 132 g = 150. g soln × 1 mL soln1.08 g soln = 138.9 mL = 0.1389 L solution
Dr. Karmach

Guided example: solution

18.0 g KNO₃ + 132 g water · density 1.08 g/mL · molar mass 101.11 g/mol
Step 1 · Pick a basis Step 2 · Density links volume and mass
18.0 g + 132 g = 150. g soln × 1 mL soln1.08 g soln = 138.9 mL = 0.1389 L solution
Step 3 · Find the solute Step 4 · Divide by the asked amount
18.0 g KNO₃ × 1 mol KNO₃101.11 g KNO₃ = 0.178 mol KNO₃ · M = 0.178 mol KNO₃0.1389 L solution = 1.28 M
Dr. Karmach

Guided example: solution

18.0 g KNO₃ + 132 g water · density 1.08 g/mL · molar mass 101.11 g/mol
Step 1 · Pick a basis Step 2 · Density links volume and mass
18.0 g + 132 g = 150. g soln × 1 mL soln1.08 g soln = 138.9 mL = 0.1389 L solution
Step 3 · Find the solute Step 4 · Divide by the asked amount
18.0 g KNO₃ × 1 mol KNO₃101.11 g KNO₃ = 0.178 mol KNO₃ · M = 0.178 mol KNO₃0.1389 L solution = 1.28 M
Read as 150. mL, the batch gives 1.19 M. Denser than water, it fills only 139 mL: 1.28 M. ✓

Dr. Karmach

Practice 3

100. g sucrose + 150. mL water · syrup 1.18 g/mL · sucrose 342.30 g/mol
water: 1.00 g/mL · wanted: molarity of the syrup

A canning syrup is made by stirring 100. g of sucrose into 150. mL of water. The finished syrup has a density of 1.18 g/mL. What is its molarity?

  1. 1.95
  2. 0.990
  3. 2.30
  4. 1.17
  5. 1.38
Dr. Karmach

Practice 3 answer: E

100. g sucrose + 150. mL water · syrup 1.18 g/mL · sucrose 342.30 g/mol
150. mL × 1.00 g/mL = 150. g water · 250. g syrup · 100. g ÷ 342.30 = 0.2921 mol
250. g syrup × 1 mL syrup1.18 g syrup = 0.2119 L · M = 0.2921 mol0.2119 L = 1.38 M · answer E

A used the water's 150. mL as the syrup's volume: 0.2921 ÷ 0.150 = 1.95. D skipped the density: 0.2921 ÷ 0.250 = 1.17. B multiplied by it: 0.2921 ÷ 0.295 = 0.990. C left out the sucrose: 0.2921 ÷ 0.1271 = 2.30.

The sugar adds mass, and the syrup fills 212 mL, more than the 150. mL of water: 1.38 M. ✓

Dr. Karmach

Check yourself

  1. A drum reads 36% by mass, density 1.18 g/mL. Name the two conversion factors that carry that label to a molarity, and say which one makes 1 L weigh more than 1000 g.
  2. Molarity and molality both describe one bottle. Which divides the moles by liters of solution, and which by kilograms of solvent, and which of the two needs the density to reach the other?

Freezing-point depression and boiling-point elevation count particles per kilogram of solvent: molality. Turning a labeled molarity or mass percent into molality is the first move in every colligative-property problem.

Dr. Karmach

6 · Colloids

Classify a mixture as a solution, a colloid, or a suspension from particle size, light scattering, and settling, and name a colloid's type from its dispersed phase and its medium.

Dr. Karmach

One flashlight, three mixtures

Fog turns headlight beams into visible shafts; clear air leaves them invisible. Muddy water settles clear overnight; milk stays milk for weeks. Particle size decides both.

Dr. Karmach

Mixtures you already sort

salt water: homogeneous · sand in water: heterogeneous
one uniform phase, even under a microscope · grains visible, settle to the bottom
milk: homogeneous to the eye
under a microscope: fat droplets spread through water

The eye sorts mixtures as homogeneous or heterogeneous. Milk passes for homogeneous, yet its droplets are far larger than molecules. Mixtures like milk form a third class: colloids.

Dr. Karmach

Particle size sets the class

solution: particles under 1 nm
beam invisible · never settles · passes filter paper
colloid: particles 1 to 1000 nm
beam scattered · never settles · passes filter paper
suspension: particles over 1000 nm
cloudy while mixed · settles on standing · caught by filter paper

The size of the dispersed particles decides what a mixture does: whether a beam scatters, whether particles settle, whether filter paper stops them.

memory hook: scatters? not a solution · settles? a suspension
scatters but never settles: a colloid
Dr. Karmach

The Tyndall effect

beam → salt water: crosses unseen
dissolved particles under 1 nm: too small to scatter light
beam → milk: a glowing shaft
colloid particles 1 to 1000 nm: large enough to scatter light in every direction

Colloid particles scatter light sideways, so a beam becomes visible inside the mixture: the Tyndall effect. A scattered beam that never settles marks a colloid. A scattered beam that clears on standing marks a suspension.

Dr. Karmach

Colloid types: dispersed phase in medium

fog: liquid in gas → an aerosol · smoke: solid in gas → also an aerosol
whipped cream: gas in liquid → a foam · marshmallow: gas in solid → a solid foam
milk and mayonnaise: liquid in liquid → emulsions · paint: solid in liquid → a sol
gelatin: liquid in a solid protein network → a gel

Naming the dispersed phase and then the medium names the colloid type. Milk scatters light for the same reason fog does: droplets of one phase dispersed in another.

memory hook: "aero" means air, so an aerosol is anything dispersed IN a gas
a foam traps gas inside · an emulsion is liquid in liquid · a sol is solid in liquid
Dr. Karmach

Emulsifying agents

oil + vinegar → two layers · oil + vinegar + egg yolk → mayonnaise
the yolk's lecithin coats every oil droplet: an emulsifying agent
soap: a nonpolar tail on a polar head
tail dissolves into the grease droplet · head faces the water · the droplet stays dispersed

Like dissolves like keeps oil out of vinegar. An emulsifying agent sits at the boundary, one end in each liquid, coating droplets so they cannot rejoin. Soap does the same job on grease.

Dr. Karmach

The method

  1. Run the beam test: no visible track → solution.
  2. Check settling and the filter: settles or caught on filter paper → suspension. Neither → colloid.
  3. Name the colloid type: dispersed phase first, then the medium.

Dr. Karmach

Guided example: hand lotion

hand lotion: tiny oil droplets spread through water
laser beam: a bright line · filter paper: nothing caught · a week standing: no settling

Lotion looks perfectly uniform, so a common first call is solution. Classify the lotion. If it is a colloid, name its type.

Dr. Karmach

Guided example: the class

hand lotion: tiny oil droplets spread through water
laser beam: a bright line · filter paper: nothing caught · a week standing: no settling

Step 1 · Run the beam test

The beam leaves a bright line. Particles large enough to scatter light are present, so the lotion is not a solution.

Dr. Karmach

Guided example: the class

hand lotion: tiny oil droplets spread through water
laser beam: a bright line · filter paper: nothing caught · a week standing: no settling
Step 1 · Run the beam test Step 2 · Check settling and the filter
bright line · nothing caught · no settling → a colloid
particles between 1 and 1000 nm

Nothing settles and the filter paper catches nothing. The droplets sit below suspension size.

Dr. Karmach

Guided example: the class

hand lotion: tiny oil droplets spread through water
laser beam: a bright line · filter paper: nothing caught · a week standing: no settling
Step 1 · Run the beam test Step 2 · Check settling and the filter
bright line · nothing caught · no settling → a colloid
particles between 1 and 1000 nm
The lotion scatters light but never settles: a colloid, whatever its uniform look suggests.
Dr. Karmach

Guided example: the type

hand lotion: tiny oil droplets spread through water
from the tests: bright line · nothing caught · no settling → a colloid

Step 3 · Name the colloid type

oil droplets (liquid) dispersed in water (liquid) → an emulsion
dispersed phase first · then the medium

Liquid in liquid is an emulsion, the same type as milk.

Dr. Karmach

Guided example: the type

hand lotion: tiny oil droplets spread through water
from the tests: bright line · nothing caught · no settling → a colloid
Step 3 · Name the colloid type
oil droplets (liquid) dispersed in water (liquid) → an emulsion
dispersed phase first · then the medium
Uniform to the eye, yet a colloid. The beam decides the class; the two phases decide the type.

Dr. Karmach

Practice 1

shaving cream: tiny gas bubbles spread through a liquid soap film
a colloid · wanted: its type

Which colloid type is shaving cream?

  1. A foam
  2. An aerosol
  3. An emulsion
  4. A sol
Dr. Karmach

Practice 1 · answer: A

gas dispersed in a liquid → a foam (answer A)
name the dispersed phase first, then the medium

B swapped phase and medium: an aerosol is liquid or solid dispersed in a gas, like fog or a spray. C judged by the creamy look; an emulsion is liquid in liquid, like milk. D named the wrong dispersed phase; a sol is solid in liquid, like paint.

Dr. Karmach

Practice 1 · answer: A

gas dispersed in a liquid → a foam (answer A)
name the dispersed phase first, then the medium
Gas bubbles held in a liquid make a foam, the same type as whipped cream.

Dr. Karmach

Practice 2

sample A: ground coffee stirred into cold water
laser beam: a bright line · filter paper: solid caught · overnight: a layer settles
sample B: egg white stirred into water
laser beam: a bright line · filter paper: nothing caught · a week standing: no settling

Classify each sample from its three test results.

  1. A: colloid · B: suspension
  2. A: suspension · B: colloid
  3. A: colloid · B: colloid
  4. A: suspension · B: solution
Dr. Karmach

Practice 2 · answer: B

A: settles and is caught by filter paper → a suspension · B: scatters but never settles → a colloid
answer B · both scatter the beam, so the beam alone cannot tell them apart

A swapped the two: a colloid never settles, and sample A drops a layer overnight. C sorted by the beam alone; both glow, but only B keeps its particles dispersed. D read B's clear filter paper and no settling as dissolved, but dissolved particles leave no beam track.

Dr. Karmach

Practice 2 · answer: B

A: settles and is caught by filter paper → a suspension · B: scatters but never settles → a colloid
answer B · both scatter the beam, so the beam alone cannot tell them apart
Run the tests in order for each: the beam rules out a solution for both; settling and the filter paper then split a suspension from a colloid.

Dr. Karmach

Practice 3

A: India ink in water, solid carbon particles spread through it · B: contact-lens saline
laser beam: a glowing shaft in A, unseen in B · filter paper: both pass · a week standing: neither settles

Classify each sample, and name the type of any colloid.

  1. A: suspension · B: solution
  2. A: colloid, an emulsion · B: solution
  3. A: colloid, a sol · B: colloid
  4. A: solution · B: solution
  5. A: colloid, a sol · B: solution
Dr. Karmach

Practice 3 · answer: E

A: glowing shaft, passes the filter, never settles → colloid · carbon (solid) in water (liquid) → a sol
B: beam unseen → solution · answer E

A sorted the ink by the beam alone; a suspension also settles and is caught, and A did neither. B took the ink, a liquid from the bottle, as the dispersed phase; the particles scattering the beam are solid carbon, and an emulsion is liquid in liquid, like milk. C sorted the saline by settling and the filter alone; solutions pass both too, and only the beam splits them. D read A's clear filter and no settling as dissolved; dissolved particles leave no beam track.

Dr. Karmach

Practice 3 · answer: E

A: glowing shaft, passes the filter, never settles → colloid · carbon (solid) in water (liquid) → a sol
B: beam unseen → solution · answer E
Beam first for each sample. Only the sample that scatters goes on to a type: solid in liquid, a sol, the same type as paint.

Dr. Karmach

Check yourself

  1. A flashlight beam glows inside two different glasses. After a day, one glass has a solid layer on the bottom and the other is unchanged. Classify each mixture.
  2. Mayonnaise is mostly oil and vinegar, two liquids that separate on their own. Name the job the egg yolk does, and what each end of such a molecule holds onto.

Particle size returns in colligative properties: boiling and freezing points move with the number of dissolved particles, and a colloid's few large particles barely move either one.

Dr. Karmach

7 · Freezing Point & Boiling Point

Count the dissolved particles with the van't Hoff factor i, then use ΔTf = i·Kf·m and ΔTb = i·Kb·m to find how far a solute lowers the freezing point and raises the boiling point of water.

Dr. Karmach

Salt on ice, antifreeze in a radiator

Scatter salt on a frozen walk and the ice melts below 0 °C. Antifreeze keeps a radiator from freezing in winter and boiling over in summer.

Dr. Karmach

Freezing lower, boiling higher

Freezing builds an ordered lattice; any particle blocks it, so the solution freezes colder. Solute also crowds the liquid's surface; fewer molecules escape, so the liquid must run hotter to boil. Number matters, not identity.

memory hook: a solute stretches the liquid range both ways
freezes below the pure solvent · boils above it · more particles, more stretch
Dr. Karmach

The size of the shift

water: Kf = 1.86 °C·kg/mol   Kb = 0.512 °C·kg/mol
ΔTf = i · Kf · m (down) · ΔTb = i · Kb · m (up)

Each equation multiplies the particle count i, the solvent constant K, and the molality m. Kf sets the freezing shift, Kb the boiling shift. A bigger i or higher m shifts more.

Dr. Karmach

Recap: what a solute becomes in water

NaCl(s) → Na⁺(aq) + Cl⁻(aq)
strong electrolyte · 1 + 1 = 2 particles
CaCl₂(s) → Ca²⁺(aq) + 2 Cl⁻(aq)
strong electrolyte · 1 + 2 = 3 particles
C₁₂H₂₂O₁₁(s) → C₁₂H₂₂O₁₁(aq)
sugar · nonelectrolyte · dissolves whole · 1 particle

A strong electrolyte dissociates into separate ions. A nonelectrolyte dissolves as whole molecules. Dissociation sorts solutes into these classes. Freezing and boiling shifts respond only to the particle count.

Dr. Karmach

The van't Hoff factor i

i counts how many particles each formula unit releases. A molecular solute stays whole, so i = 1. NaCl gives two ions, CaCl₂ three. More particles mean a bigger shift.

memory hook: i = the pieces the formula splits into
glucose 1 · NaCl 2 · CaCl₂ 3 (one Ca²⁺, two Cl⁻) · Na₂SO₄ 3 (two Na⁺, one SO₄²⁻)
Dr. Karmach

The method

  1. Count the particles. Read i from the formula.
  2. Find the molality. mol solute ÷ kg SOLVENT.
  3. Multiply i · K · m. Kf 1.86 freezing, Kb 0.512 boiling.
  4. Shift from pure water. 0 − ΔTf, or 100 + ΔTb.
Dr. Karmach

Worked example 1: freezing point of antifreeze

ΔTf = i · Kf · m
given: 1.50 molal ethylene glycol · Kf = 1.86 °C·kg/mol · wanted: ΔTf

A radiator holds 1.50 molal ethylene glycol in water. Ethylene glycol is molecular: it dissolves without splitting into ions.

Count the particles, then multiply.

Dr. Karmach

Worked example 1: solution

ΔTf = i · Kf · m
given: 1.50 molal ethylene glycol · Kf = 1.86 °C·kg/mol · wanted: ΔTf

Step 1 · Count the particles

Ethylene glycol is molecular. It dissolves as whole molecules, so i = 1.

Dr. Karmach

Worked example 1: solution

ΔTf = i · Kf · m
given: 1.50 molal ethylene glycol · Kf = 1.86 °C·kg/mol · wanted: ΔTf
Step 1 · Count the particles Step 2 · Find the molality Step 3 · Multiply i · K · m m = 1.50 mol/kg, given.
ΔTf = 1 × 1.86 °C·kgmol × 1.50 molkg = 2.79 °C
A molecular solute still shifts the point. The freezing point drops to 0 − 2.79 = −2.79 °C. Freezing point goes DOWN. ✓
Dr. Karmach

Worked example 1: the route on the map

ΔTf = 1 × 1.86 × 1.50 = 2.79 °C
ethylene glycol, molecular: i = 1 · m given · the change is asked, so stop at ΔTf

One multiplication. A molecular solute keeps i = 1, and m was given. ✓
Dr. Karmach

Worked example 2: freezing point of a salt solution

ΔTf = i · Kf · m
given: 1.20 molal NaCl · Kf = 1.86 °C·kg/mol · wanted: ΔTf

A 1.20 molal NaCl solution is spread on an icy road. A common first attempt multiplies Kf by m and stops.

Count the particles, then multiply.

Dr. Karmach

Worked example 2: solution

ΔTf = i · Kf · m
given: 1.20 molal NaCl · Kf = 1.86 °C·kg/mol · wanted: ΔTf

A common first attempt

ΔTf = 1.86 °C·kgmol × 1.20 molkg = 2.23 °C ✗

NaCl is not one particle. This left out i.

Dr. Karmach

Worked example 2: solution

ΔTf = i · Kf · m
given: 1.20 molal NaCl · Kf = 1.86 °C·kg/mol · wanted: ΔTf
A common first attempt
ΔTf = 1.86 °C·kgmol × 1.20 molkg = 2.23 °C ✗
Step 1 · Count the particles

NaCl dissolves into Na⁺ and Cl⁻: two particles per formula unit, so i = 2.

Dr. Karmach

Worked example 2: solution

ΔTf = i · Kf · m
given: 1.20 molal NaCl · Kf = 1.86 °C·kg/mol · wanted: ΔTf
A common first attempt
ΔTf = 1.86 °C·kgmol × 1.20 molkg = 2.23 °C ✗
Step 1 · Count the particles Step 2 · Find the molality Step 3 · Multiply i · K · m
ΔTf = 2 × 1.86 °C·kgmol × 1.20 molkg = 4.46 °C
Two ions double the depression to 4.46 °C. Freezing point goes DOWN, to −4.46 °C. ✓
Dr. Karmach

Worked example 2: the route on the map

ΔTf = 2 × 1.86 × 1.20 = 4.46 °C
NaCl gives Na⁺ + Cl⁻: i = 2 · m given · stop at ΔTf

The same route as example 1. Only step 1 changed: two ions, twice the shift. ✓
Dr. Karmach

Take-home: count the particles

1.20 molal NaCl · Kf = 1.86
forgot i (i = 1): 1.86 × 1.20 = 2.23 °C ✗ · counted i = 2: 2 × 1.86 × 1.20 = 4.46 °C ✓

An ionic solute breaks into ions, and each ion counts. Skip i and the depression comes out too small. That is the usual mistake. Read i from the formula before multiplying.

Dr. Karmach

Practice 1

ΔTf = i · Kf · m
given: 0.900 molal KCl · Kf = 1.86 °C·kg/mol · wanted: ΔTf

A 0.900 molal KCl solution is used as a de-icer. What is its freezing-point depression, in °C?

  1. 1.67
  2. 0.922
  3. 3.35
  4. 1.80
Dr. Karmach

Practice 1 answer: C

ΔTf = i · Kf · m
given: 0.900 molal KCl · i = 2 · Kf = 1.86 °C·kg/mol
ΔTf = 2 × 1.86 °C·kgmol × 0.900 molkg = 3.35 °C · answer C

A forgot i: 1.86 × 0.900 = 1.67 °C uses i = 1, but KCl gives two ions. B used Kb: 2 × 0.512 × 0.900 = 0.922 °C is the boiling constant, not the freezing one. D stopped at i × m: 2 × 0.900 = 1.80 mol/kg counts the dissolved particles but never multiplies by Kf.

Two ions and Kf = 1.86 give a 3.35 °C depression. The freezing point drops to −3.35 °C. Freezing point goes DOWN. ✓
Dr. Karmach

Worked example 3: new freezing point from grams

new freezing point = 0 °C − ΔTf
given: 41.6 g CaCl₂ (110.98 g/mol) · 500. g water · Kf = 1.86 °C·kg/mol · wanted: the new freezing point

A road brine is mixed from 41.6 g of CaCl₂ and 500. g of water. A common first attempt reports the depression itself as the freezing point.

Count the particles, find the molality, then shift from 0 °C.

Dr. Karmach

Worked example 3: solution

new freezing point = 0 °C − ΔTf
given: 41.6 g CaCl₂ (110.98 g/mol) · 500. g water · Kf = 1.86 °C·kg/mol · wanted: the new freezing point

Step 1 · Count the particles

CaCl₂ dissolves into one Ca²⁺ and two Cl⁻: three particles, so i = 3.

Dr. Karmach

Worked example 3: solution

new freezing point = 0 °C − ΔTf
given: 41.6 g CaCl₂ (110.98 g/mol) · 500. g water · Kf = 1.86 °C·kg/mol · wanted: the new freezing point
Step 1 · Count the particles Step 2 · Find the molality
41.6 g CaCl₂ × 1 mol CaCl₂110.98 g CaCl₂ = 0.3748 mol, then 0.3748 mol CaCl₂0.500 kg water = 0.7496 mol/kg

The denominator is the water alone, 0.500 kg, not the 0.5416 kg of solution.

i = 3 and m = 0.7496 mol/kg carry into the depression. ✓
Dr. Karmach

Worked example 3: the new freezing point

new freezing point = 0 °C − ΔTf
41.6 g CaCl₂ in 500. g water · i = 3 · m = 0.7496 mol/kg · Kf = 1.86 °C·kg/mol

Step 3 · Multiply i · K · m

ΔTf = 3 × 1.86 °C·kgmol × 0.7496 molkg = 4.18 °C
Dr. Karmach

Worked example 3: the new freezing point

new freezing point = 0 °C − ΔTf
41.6 g CaCl₂ in 500. g water · i = 3 · m = 0.7496 mol/kg · Kf = 1.86 °C·kg/mol
Step 3 · Multiply i · K · m
ΔTf = 3 × 1.86 °C·kgmol × 0.7496 molkg = 4.18 °C
Step 4 · Shift from pure water
new freezing point = 0 °C − 4.18 °C = −4.18 °C
The depression is 4.18 °C, but the freezing point is 0 − 4.18 = −4.18 °C, below pure water's, not +4.18. Freezing point goes DOWN. ✓
Dr. Karmach

Worked example 3: the route on the map

41.6 g CaCl₂ → 0.7496 m → ΔTf = 4.18 °C → −4.18 °C
i = 3 · molality from grams, ÷ 0.500 kg of water · the freezing point is asked: shift from 0 °C

All four steps light up. Grams add the molality step. ✓
Dr. Karmach

Your turn: new boiling point of a salt solution

new boiling point = 100 °C + ΔTb
given: 1.00 molal MgCl₂ · Kb = 0.512 °C·kg/mol · wanted: the new boiling point

MgCl₂ dissolves into one Mg²⁺ and two Cl⁻. Fill in i and Kb, find ΔTb, then add.

ΔTb = × × 1.00 = °C
Dr. Karmach

Your turn: new boiling point of a salt solution

new boiling point = 100 °C + ΔTb
given: 1.00 molal MgCl₂ · Kb = 0.512 °C·kg/mol · wanted: the new boiling point

MgCl₂ dissolves into one Mg²⁺ and two Cl⁻. Fill in i and Kb, find ΔTb, then add.

ΔTb = × × 1.00 = °C
ΔTb = 3 × 0.512 °C·kgmol × 1.00 molkg = 1.54 °C
new boiling point = 100 °C + 1.54 °C = 101.54 °C
Three ions and Kb = 0.512 raise the boiling point by 1.54 °C, to 101.54 °C. Boiling point goes UP. ✓
Dr. Karmach

Where this goes wrong

ΔTf = i · Kf · m
1.20 molal NaCl · i = 2 · Kf = 1.86 · correct ΔTf = 4.46 °C
Forgetting the particle count. Using i = 1 gives 1.86 × 1.20 = 2.23 °C. NaCl releases two ions, so i = 2 and ΔTf = 4.46 °C, twice as much.
Using Kb for a freezing problem. 2 × 0.512 × 1.20 = 1.23 °C uses the boiling constant. Freezing-point depression uses Kf = 1.86 °C·kg/mol.
Dividing by the solution's mass. 0.3748 mol CaCl₂ ÷ 0.5416 kg of solution = 0.692 m counts the salt as solvent. Molality divides by the water alone: 0.3748 ÷ 0.500 = 0.7496 m.
Reporting the depression as the temperature. A 4.18 °C depression is not a 4.18 °C freezing point. The new point is 0 − 4.18 = −4.18 °C.
Dr. Karmach

Practice 2

new freezing point = 0 °C − ΔTf
molar mass BaCl₂ 208.23 g/mol · Kf = 1.86 °C·kg/mol

A solution is made by dissolving 36.4 g of BaCl₂ in 250. g of water. What is its freezing point, in °C?

  1. −1.30
  2. 3.90
  3. −3.41
  4. −3.90
Dr. Karmach

Practice 2 answer: D

new freezing point = 0 °C − ΔTf
given: 36.4 g BaCl₂ (208.23 g/mol) · 250. g water · i = 3 · Kf = 1.86 °C·kg/mol
36.4 g ÷ 208.23 g/mol = 0.1748 mol BaCl₂ → 0.1748 mol0.250 kg water = 0.699 mol/kg
ΔTf = 3 × 1.86 × 0.699 = 3.90 °C → 0 °C − 3.90 °C = −3.90 °C · answer D

A forgot i: 0 − 1.86 × 0.699 = −1.30 °C, but BaCl₂ gives three ions. B stopped at the depression and dropped the sign: +3.90 °C is above 0 °C. C divided by the solution's mass: 0.1748 ÷ 0.2864 kg = 0.610 m, giving −3.41 °C.

Freezing point goes DOWN: −3.90 °C, below pure water's 0 °C. ✓
Dr. Karmach

Check yourself

  1. A 0.50 molal molecular-solute solution and a 0.50 molal NaCl solution are both cooled. Which freezes at the lower temperature, and why?
  2. Write ΔTb for a 0.750 molal Na₂SO₄ solution, then its boiling point. Which constant belongs in the formula?

Freezing and boiling points depend only on how many particles dissolve. A nonvolatile solute also lowers a solvent's vapor pressure, and Raoult's law sets that pressure from the solvent's mole fraction.

Dr. Karmach

8 · Raoult's Law

Use Raoult's law to find a solution's vapor pressure from the moles of solvent and nonvolatile solute, scaling the pure solvent's pressure by the solvent's mole fraction, and confirm the result falls below the pure value.

Dr. Karmach

Salted water, less steam

Two pots reach the same temperature on one burner. The pot of plain water steams hard; the salted pot gives off noticeably less. The dissolved salt holds the water back.

Dr. Karmach

A nonvolatile solute lowers vapor pressure

Vapor comes only from solvent at the surface. A nonvolatile solute takes up surface spots and never leaves, so the pressure drops with the solvent's fraction.

Dr. Karmach

Mole fraction scales a pressure

Dalton's law: Pgas = mole fraction × Ptotal
4.0 mol N₂ + 1.0 mol O₂ · mole fraction of O₂ = 1.0 ÷ 5.0 = 0.20 · P(O₂) = 0.20 × 3.0 atm = 0.60 atm

In a gas mixture, each gas's mole fraction sets its share of the total pressure. A solution works the same way. The solvent's mole fraction sets its share of P°, the pure liquid's vapor pressure.

Dr. Karmach

Raoult's law

The solution's vapor pressure is the pure value scaled by the solvent's mole fraction: P = Xsolvent · P°. Pure solvent sits at P°; every added mole of solute pulls P straight down the line.

Dr. Karmach

The pressure lowering, ΔP

ΔP = Xsolute · P° = P° − P
Xsolute = mol solute ÷ total moles · Xsolvent + Xsolute = 1

The drop from the pure pressure to the solution's is the pressure lowering, ΔP. It equals the solute's mole fraction times P°, the same amount you get as P° minus the solution's pressure.

memory hook: P follows the solvent, ΔP follows the solute
P = Xsolvent · P° · ΔP = Xsolute · P° · together they rebuild P°
Dr. Karmach

The method

  1. List what you know: moles of each and P°. Mark the unknown.
  2. Solvent's mole fraction: Xsolvent = mol solvent ÷ total.
  3. Apply Raoult's law: P = Xsolvent × P°; solve for the unknown.
  4. Check: P below P°.

Dr. Karmach

Worked example 1: vapor pressure of a solution

P = Xsolvent · P°
given: 5.00 mol water · 1.00 mol nonvolatile solute · P° = 23.8 torr · wanted: P

Sugar is a nonvolatile solute: it dissolves in water but never enters the vapor. Dissolve 1.00 mol of it in 5.00 mol of water. Find the solution's vapor pressure. (pure water: 23.8 torr)

List what you know, then take the solvent's mole fraction.

Dr. Karmach

Worked example 1: solution

P = Xsolvent · P°
given: 5.00 mol water · 1.00 mol nonvolatile solute · P° = 23.8 torr · wanted: P

Step 1 · List what you know

5.00 mol of water is the solvent. 1.00 mol of nonvolatile solute. P° = 23.8 torr. The unknown is P.

Dr. Karmach

Worked example 1: solution

P = Xsolvent · P°
given: 5.00 mol water · 1.00 mol nonvolatile solute · P° = 23.8 torr · wanted: P
Step 1 · List what you know Step 2 · Solvent's mole fraction
Xsolvent = 5.00 mol water5.00 + 1.00 mol total = 0.833
Dr. Karmach

Worked example 1: solution

P = Xsolvent · P°
given: 5.00 mol water · 1.00 mol nonvolatile solute · P° = 23.8 torr · wanted: P
Step 1 · List what you know Step 2 · Solvent's mole fraction
Xsolvent = 5.00 mol water5.00 + 1.00 mol total = 0.833
Step 3 · Apply Raoult's law
P = 0.833 × 23.8 torr = 19.8 torr
Dr. Karmach

Worked example 1: solution

P = Xsolvent · P°
given: 5.00 mol water · 1.00 mol nonvolatile solute · P° = 23.8 torr · wanted: P
Step 1 · List what you know Step 2 · Solvent's mole fraction
Xsolvent = 5.00 mol water5.00 + 1.00 mol total = 0.833
Step 3 · Apply Raoult's law
P = 0.833 × 23.8 torr = 19.8 torr
Step 4 · Check
19.8 torr sits below the pure 23.8 torr: the nonvolatile solute lowered it. ✓
Dr. Karmach

Worked example 1: the route on the map

P = Xsolvent · P° = 0.833 × 23.8 torr = 19.8 torr
given: 5.00 mol water · 1.00 mol nonvolatile solute · P° = 23.8 torr · found: P = 19.8 torr

The pressure is wanted, so the top lane: the solvent's share of the moles, times P°. ✓
Dr. Karmach

Worked example 2: the pressure lowering

P = Xsolvent · P°
given: 6.00 mol benzene · 2.00 mol nonvolatile solute · P° = 95.1 torr · wanted: ΔP and P

A nonvolatile solute is dissolved in benzene: 2.00 mol of solute in 6.00 mol of benzene. Find the pressure lowering, ΔP, and the solution's vapor pressure. (pure benzene: 95.1 torr)

List the moles, then take each mole fraction.

Dr. Karmach

Worked example 2: solution

P = Xsolvent · P°
given: 6.00 mol benzene · 2.00 mol nonvolatile solute · P° = 95.1 torr · wanted: ΔP and P

Step 1 · List what you know

6.00 mol benzene is the solvent. 2.00 mol nonvolatile solute. P° = 95.1 torr.

Dr. Karmach

Worked example 2: solution

P = Xsolvent · P°
given: 6.00 mol benzene · 2.00 mol nonvolatile solute · P° = 95.1 torr · wanted: ΔP and P
Step 1 · List what you know Step 2 · Solvent's mole fraction
Xsolvent = 6.00 mol benzene6.00 + 2.00 mol total = 0.750

The solute takes the rest: Xsolute = 2.00 ÷ 8.00 = 0.250.

Dr. Karmach

Worked example 2: solution

P = Xsolvent · P°
given: 6.00 mol benzene · 2.00 mol nonvolatile solute · P° = 95.1 torr · wanted: ΔP and P
Step 1 · List what you know Step 2 · Solvent's mole fraction
Xsolvent = 6.00 mol benzene6.00 + 2.00 mol total = 0.750
Step 3 · Apply Raoult's law
P = 0.750 × 95.1 torr = 71.3 torr
71.3 torr is below the pure 95.1 torr. ✓

Dr. Karmach

Worked example 2: the pressure lowering

ΔP = Xsolute · P° = P° − P
2.00 mol solute of 8.00 mol total · Xsolute = 0.250 · P° = 95.1 torr · P = 71.3 torr

The lowering ΔP

ΔP = Xsolute · P° = 0.250 × 95.1 = 23.8 torr
Dr. Karmach

Worked example 2: the pressure lowering

ΔP = Xsolute · P° = P° − P
2.00 mol solute of 8.00 mol total · Xsolute = 0.250 · P° = 95.1 torr · P = 71.3 torr
The lowering ΔP
ΔP = Xsolute · P° = 0.250 × 95.1 = 23.8 torr
Step 4 · Check
P° − P = 95.1 − 71.3 = 23.8 torr
Both routes to ΔP agree, and P stays below P°. ✓

Dr. Karmach

Your turn: an ethanol solution

P = Xsolvent · P°
given: 7.00 mol ethanol · 3.00 mol nonvolatile solute · P° = 43.9 torr · wanted: P

3.00 mol of a nonvolatile solute is stirred into 7.00 mol of ethanol. Fill the solvent's mole fraction, then scale P°:

Xsolvent = mol ethanol mol total = → P = × 43.9 = torr
Dr. Karmach

Your turn: an ethanol solution

P = Xsolvent · P°
given: 7.00 mol ethanol · 3.00 mol nonvolatile solute · P° = 43.9 torr · wanted: P
Xsolvent = mol ethanol mol total = → P = × 43.9 = torr
Xsolvent = 7.00 mol ethanol10.00 mol total = 0.700 → P = 0.700 × 43.9 = 30.7 torr
30.7 torr is below the pure 43.9 torr. The solute takes the rest: 43.9 − 30.7 = 13.2 torr of lowering. ✓

Dr. Karmach

Where this goes wrong

P = Xsolvent · P°
5.00 mol water · 1.00 mol solute · P° = 23.8 torr · correct P = 19.8 torr
Using the solute's mole fraction. (1.00 ÷ 6.00) × 23.8 = 3.97 torr is the pressure LOWERING, ΔP: the amount removed. The pressure that remains uses the solvent's fraction: (5.00 ÷ 6.00) × 23.8 = 19.8 torr.
Assuming the solute changes nothing. Leaving the answer at 23.8 torr. A nonvolatile solute always lowers the vapor pressure, so the result must fall below 23.8 torr, here to 19.8 torr.
Skipping the total in the fraction. (1.00 ÷ 5.00) × 23.8 = 4.76 torr divides solute by solvent. A mole fraction divides by the TOTAL moles: the solvent's fraction is 5.00 ÷ 6.00, not 1.00 ÷ 5.00.
Dr. Karmach

Guided example: vapor pressure from grams

P = Xsolvent · P°
given: 46.0 g glycerol (92.09 g/mol) · 138 g ethanol (46.07 g/mol) · P° = 43.9 torr · wanted: P

A hand-sanitizer base mixes 46.0 g of glycerol, a nonvolatile liquid, into 138 g of ethanol. Find the solution's vapor pressure. (pure ethanol: 43.9 torr)

Convert both masses to moles, then take the solvent's mole fraction.

Dr. Karmach

Guided example: solution

P = Xsolvent · P°
given: 46.0 g glycerol (92.09 g/mol) · 138 g ethanol (46.07 g/mol) · P° = 43.9 torr · wanted: P

Step 1 · List what you know

Raoult's law counts moles. Two conversion factors are needed, one molar mass for each substance.

46.0 g glycerol × 1 mol92.09 g = 0.500 mol glycerol
138 g ethanol × 1 mol46.07 g = 3.00 mol ethanol
Dr. Karmach

Guided example: solution

P = Xsolvent · P°
given: 46.0 g glycerol (92.09 g/mol) · 138 g ethanol (46.07 g/mol) · P° = 43.9 torr · wanted: P
Step 1 · List what you know
46.0 g glycerol × 1 mol92.09 g = 0.500 mol glycerol
138 g ethanol × 1 mol46.07 g = 3.00 mol ethanol
Glycerol has a third of the mass but a sixth of the moles: 3.00 ÷ 0.500 = 6.00. ✓
Dr. Karmach

Guided example: the vapor pressure

P = Xsolvent · P°
3.00 mol ethanol · 0.500 mol glycerol · P° = 43.9 torr · wanted: P

Step 2 · Solvent's mole fraction Step 3 · Apply Raoult's law

Xsolvent = 3.00 mol ethanol3.00 + 0.500 mol total = 0.857 → P = 0.857 × 43.9 torr = 37.6 torr
Dr. Karmach

Guided example: the vapor pressure

P = Xsolvent · P°
3.00 mol ethanol · 0.500 mol glycerol · P° = 43.9 torr · wanted: P
Step 2 · Solvent's mole fraction Step 3 · Apply Raoult's law
Xsolvent = 3.00 mol ethanol3.00 + 0.500 mol total = 0.857 → P = 0.857 × 43.9 torr = 37.6 torr
Step 4 · Check
37.6 torr sits below the pure 43.9 torr. ✓

Dr. Karmach

Practice 1

P = Xsolvent · P°
given: 68.4 g sucrose (342.30 g/mol) · 90.0 g water (18.02 g/mol) · P° = 23.8 torr · wanted: P

A syrup is made from 68.4 g of sucrose (342.30 g/mol) and 90.0 g of water (18.02 g/mol). What is its vapor pressure, in torr? (pure water at 25 °C: 23.8 torr)

  1. 13.5
  2. 0.916
  3. 1.62
  4. 22.9
Dr. Karmach

Practice 1 answer: D

P = Xsolvent · P°
68.4 g sucrose → 0.200 mol · 90.0 g water → 4.99 mol · total = 5.19 mol · P° = 23.8 torr
Xsolvent = 4.99 mol water(4.99 + 0.200) mol = 0.962 → P = 0.962 × 23.8 = 22.9 torr · answer D

Both masses become moles first. A took a mass fraction: 90.0 ÷ 158.4 × 23.8 = 13.5 torr, but Raoult's law counts moles. B used the solute's fraction: 0.0385 × 23.8 = 0.916 torr, the lowering not the pressure. C left the sucrose in grams: 4.99 ÷ (4.99 + 68.4) × 23.8 = 1.62 torr.

Dr. Karmach

Practice 1 answer: D

P = Xsolvent · P°
68.4 g sucrose → 0.200 mol · 90.0 g water → 4.99 mol · total = 5.19 mol · P° = 23.8 torr
Xsolvent = 4.99 mol water(4.99 + 0.200) mol = 0.962 → P = 0.962 × 23.8 = 22.9 torr · answer D
Sucrose is heavy, so 68.4 g is only 0.200 mol against 4.99 mol of water: a small lowering, 22.9 torr just under 23.8. ✓

Dr. Karmach

Worked example 3: back out the moles of solute

P = Xsolvent · P°
given: 8.0 mol benzene · solution P = 76.08 torr · P° = 95.1 torr · wanted: mol solute

A nonvolatile solute in 8.0 mol of benzene gives a solution vapor pressure of 76.08 torr. How many moles of solute are dissolved? (pure benzene: 95.1 torr)

A common first attempt: read the pressure ratio 76.08 ÷ 95.1 as the solute's share. Test it.

Dr. Karmach

Worked example 3: solution

P = Xsolvent · P°
given: 8.0 mol benzene · solution P = 76.08 torr · P° = 95.1 torr · wanted: mol solute

A common first attempt

Xsolute? = 76.08 torr95.1 torr = 0.800 → solute = 32 mol ✗

32 mol of solute against 8.0 mol of benzene, yet the pressure barely fell.

Dr. Karmach

Worked example 3: solution

P = Xsolvent · P°
given: 8.0 mol benzene · solution P = 76.08 torr · P° = 95.1 torr · wanted: mol solute
A common first attempt
Xsolute? = 76.08 torr95.1 torr = 0.800 → solute = 32 mol ✗
Step 1 · List what you know

8.0 mol benzene is the solvent. The solution reads P = 76.08 torr; pure benzene is P° = 95.1 torr. The unknown is the moles of nonvolatile solute.

Dr. Karmach

Worked example 3: solution

P = Xsolvent · P°
given: 8.0 mol benzene · solution P = 76.08 torr · P° = 95.1 torr · wanted: mol solute
A common first attempt
Xsolute? = 76.08 torr95.1 torr = 0.800 → solute = 32 mol ✗
Step 1 · List what you know Step 2 · Solvent's mole fraction
Xsolvent = PP° = 76.08 torr95.1 torr = 0.800
The pressure ratio is the solvent's share; its complement, 0.200, belongs to the solute. ✓
Dr. Karmach

Worked example 3: moles of solute

Xsolvent = mol benzene ÷ total
8.0 mol benzene · Xsolvent = 0.800 · P = 76.08 torr · P° = 95.1 torr

Step 3 · Apply Raoult's law

Solve Xsolvent = mol benzene ÷ total for the total, then subtract the benzene:

total = 8.0 mol benzene0.800 = 10.0 mol → solute = 10.0 − 8.0 = 2.0 mol
Dr. Karmach

Worked example 3: moles of solute

Xsolvent = mol benzene ÷ total
8.0 mol benzene · Xsolvent = 0.800 · P = 76.08 torr · P° = 95.1 torr
Step 3 · Apply Raoult's law
total = 8.0 mol benzene0.800 = 10.0 mol → solute = 10.0 − 8.0 = 2.0 mol
Step 4 · Check
solute share = 1 − 0.800 = 0.200 → 0.200 × 10.0 = 2.0 mol ✓
Both fractions give 2.0 mol; the 32 mol read the solvent's share as the solute's. ✓

Dr. Karmach

Take-home: use the solvent's mole fraction

solute's fraction → the lowering: (1.00 ÷ 6.00) × 23.8 = 3.97 torr ✗
5.00 mol water · 1.00 mol solute · P° = 23.8 torr · this is ΔP, not the pressure
solvent's fraction → the pressure: (5.00 ÷ 6.00) × 23.8 = 19.8 torr ✓
P = Xsolvent · P° · the two add back to P°: 3.97 + 19.8 = 23.8 torr

Raoult's law multiplies P° by the SOLVENT's mole fraction. The solute's fraction gives the drop, ΔP: the amount removed, not the pressure that remains.

Dr. Karmach

Practice 2

ΔP = Xsolute · P°
given: 12.0 mol acetone · lowering ΔP = 46.2 torr · P° = 231 torr · wanted: mol solute

A nonvolatile solute dissolved in 12.0 mol of acetone lowers the vapor pressure by 46.2 torr. How many moles of solute are dissolved? (pure acetone: 231 torr)

  1. 3.00
  2. 15.0
  3. 48.0
  4. 60.0
Dr. Karmach

Practice 2 answer: A

ΔP = Xsolute · P°
12.0 mol acetone · ΔP = 46.2 torr · P° = 231 torr
Xsolute = 46.2 torr231 torr = 0.200 → Xsolvent = 0.800 → total = 12.0 mol0.800 = 15.0 mol → solute = 15.0 − 12.0 = 3.00 mol · answer A

The lowering gives the solute's share; the acetone holds the rest. B stopped at the total: 15.0 mol counts the acetone too. C read 0.200 as the solvent's share: 12.0 ÷ 0.200 = 60.0 total, then 60.0 − 12.0 = 48.0. D divided the acetone by the solute's share and stopped: 12.0 ÷ 0.200 = 60.0.

Dr. Karmach

Practice 2 answer: A

ΔP = Xsolute · P°
12.0 mol acetone · ΔP = 46.2 torr · P° = 231 torr
Xsolute = 46.2 torr231 torr = 0.200 → Xsolvent = 0.800 → total = 12.0 mol0.800 = 15.0 mol → solute = 15.0 − 12.0 = 3.00 mol · answer A
3.00 mol of solute in 15.0 mol total is a 0.200 share, and 0.200 × 231 = 46.2 torr, the lowering given. ✓

Dr. Karmach

Practice 3

P = Xsolvent · P°
given: 215 g chloroform (CHCl₃, 119.38 g/mol) · solution P = 157.6 torr · P° = 197.0 torr · wanted: mol solute

A nonvolatile solute is dissolved in 215 g of chloroform (CHCl₃, 119.38 g/mol). The solution's vapor pressure is 157.6 torr. How many moles of solute are dissolved? (pure chloroform: 197.0 torr)

  1. 2.25
  2. 53.8
  3. 0.360
  4. 0.450
  5. 7.20
Dr. Karmach

Practice 3 answer: D

P = Xsolvent · P°
215 g chloroform (119.38 g/mol) → 1.801 mol · P = 157.6 torr · P° = 197.0 torr · wanted: mol solute
Xsolvent = 157.6 torr197.0 torr = 0.8000 → total = 1.801 mol CHCl₃0.8000 = 2.251 mol
solute = 2.251 mol − 1.801 mol CHCl₃ = 0.450 mol · answer D

A stopped at the total, which counts the chloroform too. B kept the chloroform in grams: 215 ÷ 0.8000 − 215 = 53.8. C took the solute's 0.2000 share of the chloroform alone: 0.2000 × 1.801 = 0.360. E read 0.8000 as the solute's share: 1.801 ÷ 0.2000 − 1.801 = 7.20.

Dr. Karmach

Practice 3 answer: D

P = Xsolvent · P°
215 g chloroform (119.38 g/mol) → 1.801 mol · P = 157.6 torr · P° = 197.0 torr · wanted: mol solute
Xsolvent = 157.6 torr197.0 torr = 0.8000 → total = 1.801 mol CHCl₃0.8000 = 2.251 mol
solute = 2.251 mol − 1.801 mol CHCl₃ = 0.450 mol · answer D
0.450 of 2.251 mol is a 0.200 share: 0.200 × 197.0 = 39.4 torr, the drop to 157.6 torr. ✓

Dr. Karmach

Check yourself

  1. A solution holds 8.00 mol of water and 2.00 mol of a nonvolatile solute; pure water is 23.8 torr. Which mole fraction scales P°, and what is the solution's vapor pressure?
  2. A nonvolatile solute drops a solvent's vapor pressure from 90.0 torr to 72.0 torr. Write the pressure lowering ΔP, and give the solvent's mole fraction.

A nonvolatile solute sets how much solvent escapes. A gas does the reverse from outside: Henry's law sets how much gas dissolves into a solvent, and that amount climbs with the gas's pressure above the liquid.

Dr. Karmach

9 · Henry's Law

Use Henry's law (a gas's solubility is directly proportional to its partial pressure, S₁/P₁ = S₂/P₂) to find a new solubility, or the pressure that produces it, at constant temperature.

Dr. Karmach

Open a soda and it erupts

Crack the tab on a shaken can and it hisses, then foams over. Sealed, the fizz stayed down in the drink. Opened, the gas escapes all at once.

Dr. Karmach

More gas overhead, more gas dissolved

At constant temperature, a gas's solubility (how much dissolves) rises and falls in step with its partial pressure. More gas overhead drives more into solution.

Dr. Karmach

Solubility is proportional to pressure

Plot the dissolved amount against the partial pressure: the points fall on a straight line through the origin. Double the pressure, double the dissolved gas. The slope depends only on the gas and temperature.

Dr. Karmach

Henry's law is direct, not inverse

Raise the pressure and solubility rises with it. The two move the same way. Boyle's law is the opposite: squeeze a trapped gas and its volume shrinks. Same variable, but opposite behavior.

memory hook: pressure up, gas in · pressure down, gas out
a sealed soda holds its fizz · an opened one goes flat
Dr. Karmach

The method

  1. Identify given and wanted. Mark the unknown.
  2. Set up the proportion. Same gas, constant temperature: S₁/P₁ = S₂/P₂.
  3. Rearrange for the unknown.
  4. Substitute and check. More pressure means more dissolved gas.
Dr. Karmach

Worked example 1: more pressure, more dissolved

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L · P₁ = 1.0 atm · P₂ = 4.0 atm · same gas, constant temperature · wanted: S₂

Water sits under carbon dioxide. At 1.0 atm of CO₂, 1.45 g/L dissolves. The CO₂ pressure is raised to 4.0 atm at constant temperature. Find the new solubility.

Identify the given and the wanted, and note what is held fixed.

Dr. Karmach

Worked example 1: solution

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L · P₁ = 1.0 atm · P₂ = 4.0 atm · same gas, constant temperature · wanted: S₂

Step 1 · Identify given and wanted

S₁ = 1.45 g/L at P₁ = 1.0 atm. P₂ = 4.0 atm. The gas and the temperature do not change. The unknown is S₂.

Dr. Karmach

Worked example 1: solution

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L · P₁ = 1.0 atm · P₂ = 4.0 atm · same gas, constant temperature · wanted: S₂
Step 1 · Identify given and wanted Step 2 · Set up the proportion

Same gas, constant temperature, so S/P stays constant: S₁/P₁ = S₂/P₂.

Dr. Karmach

Worked example 1: solution

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L · P₁ = 1.0 atm · P₂ = 4.0 atm · same gas, constant temperature · wanted: S₂
Step 1 · Identify given and wanted Step 2 · Set up the proportion Step 3 · Rearrange for the unknown
S₁/P₁ = S₂/P₂ → S₂ = S₁ × P₂P₁

The new pressure goes on top: solubility climbs with pressure.

Dr. Karmach

Worked example 1: solution

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L · P₁ = 1.0 atm · P₂ = 4.0 atm · same gas, constant temperature · wanted: S₂
Step 1 · Identify given and wanted Step 2 · Set up the proportion Step 3 · Rearrange for the unknown
S₁/P₁ = S₂/P₂ → S₂ = S₁ × P₂P₁
Step 4 · Substitute and check
S₂ = 1.45 g/L × 4.0 atm1.0 atm = 5.80 g/L
Pressure quadrupled at constant temperature, so four times as much CO₂ dissolves: 1.45 → 5.80 g/L. ✓
Dr. Karmach

Worked example 1: the route on the strip

S₁/P₁ = S₂/P₂
given: 1.45 g/L at 1.0 atm · P₂ = 4.0 atm · found: S₂ = 5.80 g/L

A solubility is wanted, so the top lane: the new pressure goes on top. The pressure rose, and the solubility rose with it. ✓
Dr. Karmach

Worked example 2: pressure released, gas comes out

S₁/P₁ = S₂/P₂
given: S₁ = 5.80 g/L · P₁ = 4.0 atm · P₂ = 1.0 atm · same gas, constant temperature · wanted: S₂

A carbonation tank holds water under 4.0 atm of CO₂, dissolving 5.80 g/L. The CO₂ pressure is bled down to 1.0 atm. Find the new dissolved amount.

List the given and the wanted, and mark what is held fixed.

Dr. Karmach

Worked example 2: solution

S₁/P₁ = S₂/P₂
given: S₁ = 5.80 g/L · P₁ = 4.0 atm · P₂ = 1.0 atm · same gas, constant temperature · wanted: S₂

Step 1 · Identify given and wanted

S₁ = 5.80 g/L at P₁ = 4.0 atm. P₂ = 1.0 atm. The gas and the temperature are unchanged. The unknown is S₂.

Dr. Karmach

Worked example 2: solution

S₁/P₁ = S₂/P₂
given: S₁ = 5.80 g/L · P₁ = 4.0 atm · P₂ = 1.0 atm · same gas, constant temperature · wanted: S₂
Step 1 · Identify given and wanted Step 2 · Set up the proportion

Same gas, constant temperature, so S/P stays constant: S₁/P₁ = S₂/P₂.

Dr. Karmach

Worked example 2: solution

S₁/P₁ = S₂/P₂
given: S₁ = 5.80 g/L · P₁ = 4.0 atm · P₂ = 1.0 atm · same gas, constant temperature · wanted: S₂
Step 1 · Identify given and wanted Step 2 · Set up the proportion Step 3 · Rearrange for the unknown
S₁/P₁ = S₂/P₂ → S₂ = S₁ × P₂P₁

The new pressure still goes on top; here it is the smaller one.

Dr. Karmach

Worked example 2: solution

S₁/P₁ = S₂/P₂
given: S₁ = 5.80 g/L · P₁ = 4.0 atm · P₂ = 1.0 atm · same gas, constant temperature · wanted: S₂
Step 1 · Identify given and wanted Step 2 · Set up the proportion Step 3 · Rearrange for the unknown
S₁/P₁ = S₂/P₂ → S₂ = S₁ × P₂P₁
Step 4 · Substitute and check
S₂ = 5.80 g/L × 1.0 atm4.0 atm = 1.45 g/L
Pressure dropped to a quarter, so only a quarter of the CO₂ stays dissolved: 5.80 → 1.45 g/L. The rest, 5.80 − 1.45 = 4.35 g from every liter, fizzes out. ✓
Dr. Karmach

Worked example 2: the route on the strip

S₁/P₁ = S₂/P₂
given: 5.80 g/L at 4.0 atm · P₂ = 1.0 atm · found: S₂ = 1.45 g/L · 4.35 g released per liter

The top lane gives the new solubility, 1.45 g/L. The bottom lane turns the drop into gas released: (5.80 − 1.45) g/L × 1 L = 4.35 g. ✓
Dr. Karmach

Your turn: nitrogen under pressure

S₁/P₁ = S₂/P₂
given: S₁ = 0.019 g/L · P₁ = 1.0 atm · P₂ = 5.0 atm · same gas, constant temperature · wanted: S₂

Nitrogen dissolves at 0.019 g/L under 1.0 atm of N₂. A reactor blankets it at 5.0 atm.

S₂ = 0.019 g/L × atm atm = g/L

Put the new pressure on top and the old pressure below, then compute.

Dr. Karmach

Your turn: nitrogen under pressure

S₁/P₁ = S₂/P₂
given: S₁ = 0.019 g/L · P₁ = 1.0 atm · P₂ = 5.0 atm · same gas, constant temperature · wanted: S₂

Nitrogen dissolves at 0.019 g/L under 1.0 atm of N₂. A reactor blankets it at 5.0 atm.

S₂ = 0.019 g/L × atm atm = g/L

Put the new pressure on top and the old pressure below, then compute.

S₂ = 0.019 g/L × 5.0 atm1.0 atm = 0.095 g/L
Pressure rose fivefold, so five times as much N₂ dissolves: 0.019 → 0.095 g/L. ✓
Dr. Karmach

Where this goes wrong

S₁/P₁ = S₂/P₂
1.45 g/L of CO₂ at 1.0 atm, raised to 4.0 atm · correct S₂ = 5.80 g/L
Inverting the proportion. Pressure rose from 1.0 to 4.0 atm, so more CO₂ dissolves. Writing 1.45 × (1.0/4.0) = 0.363 g/L predicts less: that is Boyle's inverse ratio. Henry's law is direct: the new pressure goes on top, (P₂/P₁).
Adding the pressure change. Solubility is a proportion, not a sum. Adding the change, 1.45 + (4.0 − 1.0) = 4.45 g/L, tacks atm onto g/L. Multiply by the pressure ratio instead.
Assuming no change. The partial pressure quadrupled, so the dissolved amount cannot stay 1.45 g/L. Raising the pressure forces more gas in; the solubility must rise.
Dr. Karmach

Practice 1

S₁/P₁ = S₂/P₂
given: S₁ = 0.0430 g/L · P₁ = 1.00 atm · P₂ = 3.00 atm · same gas, constant temperature · wanted: S₂

Oxygen dissolves at 0.0430 g/L under 1.00 atm of O₂. Under a 3.00 atm atmosphere of O₂ at the same temperature, what is its solubility, in g/L?

  1. 0.0143
  2. 0.0860
  3. 0.129
  4. 0.0430
Dr. Karmach

Practice 1 answer: C

S₁/P₁ = S₂/P₂
O₂ · S₁ = 0.0430 g/L at P₁ = 1.00 atm · P₂ = 3.00 atm · constant temperature
S₂ = 0.0430 g/L × 3.00 atm1.00 atm = 0.129 g/L · answer C

A inverted the proportion like Boyle's law: 0.0430 × (1.00/3.00) = 0.0143 g/L, less dissolved though the pressure rose. B scaled by the pressure change: 0.0430 × (3.00 − 1.00)/1.00 = 0.0860 g/L; the ratio takes the new pressure, 3.00 atm, not the 2.00 atm increase. D assumed no change: at 3.00 atm the solubility cannot stay 0.0430 g/L.

Pressure tripled, so three times as much O₂ dissolves: 0.0430 → 0.129 g/L. ✓
Dr. Karmach

Worked example 3: the pressure to reach a target

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L at P₁ = 1.0 atm · target S₂ = 8.70 g/L · same gas, constant temperature · wanted: P₂

A bottler wants 8.70 g/L of CO₂ dissolved. At 1.0 atm only 1.45 g/L dissolves. What CO₂ partial pressure reaches the target?

A common first attempt: invert the ratio, the way Boyle's law does. Test the result.

Dr. Karmach

Worked example 3: solution

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L at P₁ = 1.0 atm · target S₂ = 8.70 g/L · wanted: P₂

A common first attempt

P₂ = 1.0 atm × 1.45 g/L8.70 g/L = 0.167 atm ✗

Less pressure to dissolve more gas is impossible. Inverting the ratio follows Boyle's law, not Henry's law.

Dr. Karmach

Worked example 3: solution

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L at P₁ = 1.0 atm · target S₂ = 8.70 g/L · wanted: P₂
A common first attempt
P₂ = 1.0 atm × 1.45 g/L8.70 g/L = 0.167 atm ✗
Step 1 · Identify given and wanted

S₁ = 1.45 g/L at P₁ = 1.0 atm. The target is S₂ = 8.70 g/L. The unknown is P₂.

Dr. Karmach

Worked example 3: solution

S₁/P₁ = S₂/P₂
given: S₁ = 1.45 g/L at P₁ = 1.0 atm · target S₂ = 8.70 g/L · wanted: P₂
A common first attempt
P₂ = 1.0 atm × 1.45 g/L8.70 g/L = 0.167 atm ✗
Step 1 · Identify given and wanted Step 2 · Set up the proportion

Same gas, constant temperature, so S/P stays constant: S₁/P₁ = S₂/P₂.

The solubility must rise sixfold, so the pressure must rise too, not fall. ✓
Dr. Karmach

Worked example 3: the pressure needed

S₁/P₁ = S₂/P₂
S₁ = 1.45 g/L · P₁ = 1.0 atm · S₂ = 8.70 g/L · wanted: P₂

Step 3 · Rearrange for the unknown

S₁/P₁ = S₂/P₂ → P₂ = P₁ × S₂S₁

The larger solubility goes on top, so the pressure comes out larger.

Dr. Karmach

Worked example 3: the pressure needed

S₁/P₁ = S₂/P₂
S₁ = 1.45 g/L · P₁ = 1.0 atm · S₂ = 8.70 g/L · wanted: P₂
Step 3 · Rearrange for the unknown
S₁/P₁ = S₂/P₂ → P₂ = P₁ × S₂S₁
Step 4 · Substitute and check
P₂ = 1.0 atm × 8.70 g/L1.45 g/L = 6.0 atm
To dissolve six times as much CO₂, the partial pressure must be six times higher: 1.0 → 6.0 atm. ✓
Dr. Karmach

Worked example 3: the route on the strip

S₁/P₁ = S₂/P₂
given: 1.45 g/L at 1.0 atm · target S₂ = 8.70 g/L · found: P₂ = 6.0 atm

A pressure is wanted, so the middle lane: the new solubility goes on top. The solubility rose sixfold, and so did the pressure. ✓
Dr. Karmach

Take-home: Henry's law is direct

inverted (Boyle's ratio): 1.0 × (1.45 / 8.70) → P = 0.167 atm
less pressure for more gas: impossible ✗
direct (Henry's law): 1.0 × (8.70 / 1.45) → P = 6.0 atm
more gas needs more pressure ✓

Solubility climbs with partial pressure, so the larger solubility goes on top of the ratio. Boyle's upside-down ratio would demand less pressure for more gas. That cannot happen.

Dr. Karmach

Practice 2

S₁/P₁ = S₂/P₂
given: CH₄ 0.0460 g/L at 2.00 atm · saturated at 6.00 atm · released to 1.50 atm · 400. mL · wanted: g CH₄ released

Deep well water is saturated with methane under 6.00 atm of CH₄. At the wellhead the CH₄ pressure falls to 1.50 atm at the same temperature. Methane dissolves at 0.0460 g/L under 2.00 atm. How many grams of CH₄ leave a 400. mL sample?

  1. 0.0552
  2. 0.0414
  3. 0.0828
  4. 41.4
Dr. Karmach

Practice 2 answer: B

S₁/P₁ = S₂/P₂
CH₄ 0.0460 g/L at 2.00 atm · 6.00 atm → 1.50 atm · 400. mL = 0.400 L
S6.00 = 0.0460 g/L × 6.002.00 = 0.138 g/L · S1.50 = 0.0460 g/L × 1.502.00 = 0.0345 g/L
Dr. Karmach

Practice 2 answer: B

S₁/P₁ = S₂/P₂
CH₄ 0.0460 g/L at 2.00 atm · 6.00 atm → 1.50 atm · 400. mL = 0.400 L
S6.00 = 0.0460 g/L × 6.002.00 = 0.138 g/L · S1.50 = 0.0460 g/L × 1.502.00 = 0.0345 g/L
(0.138 − 0.0345) gL × 0.400 L = 0.0414 g CH₄ · answer B

A is all the CH₄ dissolved at 6.00 atm: 0.138 × 0.400 = 0.0552 g. C skipped the ÷ 2.00 atm: 0.0828 g. D left mL unconverted: 41.4 g.

Pressure fell to a quarter, so three quarters leaves ✓
Dr. Karmach

Check yourself

  1. A sealed soda is opened and the gas pressing above it drops sharply. Does the dissolved gas rise or fall, and why does the drink fizz?
  2. Write S₁/P₁ = S₂/P₂ solved for S₂. When the partial pressure triples, what happens to the solubility?

Henry's law reads a dissolved amount straight off a pressure. A titration reads an unknown concentration a different way: add a measured reactant until it exactly consumes the unknown, and the volume it took fixes the concentration.

Dr. Karmach

10 · Titration Calculations

Find an unknown acid concentration from a titration by counting the titrant's millimoles, dividing out the balanced equation's base-to-acid ratio, and dividing by the acid's volume; the milliliters cancel.

Dr. Karmach

Reading the acid in vinegar

Add a drop of dye to vinegar, then drip in a known base until the color just changes. The base you used measures the acid.

Dr. Karmach

The equivalence point

Add a known base to an acid until an indicator flips; this addition is a titration. At the flip, the equivalence point, moles of OH⁻ added equal moles of H⁺ available.

Dr. Karmach

Equal millimoles in a 1:1 reaction

0.200 M × 25.00 mL = 5.00 mmol
molarity × volume, with volume in mL, counts millimoles
Macid · Vacid = Mbase · Vbase
1 : 1 acid to base · both volumes in mL, so the mL cancel

Moles equal molarity times volume. With volume in milliliters, that product counts millimoles. When an acid and base react one-to-one, their millimoles are equal.

Dr. Karmach

Polyprotic acids need the mole ratio

Macid = Mbase · Vbase ÷ (ratio · Vacid)
ratio = base units per acid unit · the mL cancel, so no liter step

A diprotic acid gives two H⁺ per unit; a triprotic gives three. Each H⁺ takes one OH⁻, so the balanced equation's coefficients set the base-to-acid ratio.

memory hook: count the H's written first
HCl 1 · H₂SO₄ 2 · H₃PO₄ 3 · that many NaOH per acid
Dr. Karmach

The method

  1. Moles of the known solution: molarity × mL gives millimoles.
  2. Apply the mole ratio: cross to the other substance with the balanced equation.
  3. Divide to finish: by its volume for a molarity, or by its molarity for a volume.
Dr. Karmach

Worked example 1: a one-to-one titration

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl titrated by 25.00 mL of 0.200 M NaOH · wanted: M of the HCl

A 20.00 mL sample of hydrochloric acid of unknown concentration is titrated with 0.200 M NaOH. The indicator changes color after 25.00 mL of base. Find the concentration of the acid.

Set it up: the base's millimoles, the 1:1 ratio, then divide by the acid's volume.

Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl · 25.00 mL of 0.200 M NaOH · wanted: M of the HCl

Three moves: the titrant's millimoles, the one-to-one ratio, then divide by the acid's volume.

Step 1 · Moles of the known solution

The base's molarity is 0.200 mmol per mL. Its volume converts to millimoles; the mL cancel:

25.00 mL base × 0.200 mmol NaOH1 mL base = 5.00 mmol NaOH
Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl · 25.00 mL of 0.200 M NaOH · wanted: M of the HCl
Step 1 · Moles of the known solution
25.00 mL base × 0.200 mmol NaOH1 mL base = 5.00 mmol NaOH
Step 2 · Apply the mole ratio

HCl and NaOH react one-to-one, so the acid supplied the same count: 5.00 mmol HCl.

Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl · 25.00 mL of 0.200 M NaOH · wanted: M of the HCl
Step 1 · Moles of the known solution
25.00 mL base × 0.200 mmol NaOH1 mL base = 5.00 mmol NaOH
Step 2 · Apply the mole ratio Step 3 · Divide to finish

The acid's millimoles over its volume give the molarity. Millimoles per milliliter is moles per liter:

M = 5.00 mmol HCl20.00 mL acid = 0.250 M HCl
Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl · 25.00 mL of 0.200 M NaOH · wanted: M of the HCl
Step 1 · Moles of the known solution
25.00 mL base × 0.200 mmol NaOH1 mL base = 5.00 mmol NaOH
Step 2 · Apply the mole ratio Step 3 · Divide to finish
M = 5.00 mmol HCl20.00 mL acid = 0.250 M HCl
The base's 25.00 mL slightly topped the acid's 20.00 mL at 0.200 M, so the acid runs a little higher: 0.250 M ✓
Dr. Karmach

Worked example 1: the route on the map

HCl + NaOH → NaCl + H₂O
given: 25.00 mL of 0.200 M NaOH · 20.00 mL HCl · found: 0.250 M HCl

The base in the buret is the known solution. Its 5.00 mmol cross 1 : 1 to the acid, then the exit divides by the acid's own 20.00 mL. ✓
Dr. Karmach

Worked example 2: a diprotic acid

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ titrated by 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄

A 20.00 mL sample of sulfuric acid is titrated with 0.250 M NaOH, and the indicator changes color after 32.00 mL of base. Sulfuric acid is diprotic: each unit gives two H⁺. Find its concentration.

A tempting shortcut: carry the base's millimoles straight to the acid's volume. Test it against the balanced equation.

Dr. Karmach

Worked example 2: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄

Three moves, but the base-to-acid ratio is no longer one.

Step 1 · Moles of the known solution

The base delivers 0.250 mmol per mL, so 32.00 mL is 8.00 mmol NaOH.

Dr. Karmach

Worked example 2: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄
Step 1 · Moles of the known solution The tempting shortcut

Carry the base's millimoles straight to the acid's volume, as if the ratio were one:

M = 8.00 mmol NaOH20.00 mL acid = 0.400 M ✗
Dr. Karmach

Worked example 2: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄
Step 1 · Moles of the known solution The tempting shortcut

Carry the base's millimoles straight to the acid's volume, as if the ratio were one:

M = 8.00 mmol NaOH20.00 mL acid = 0.400 M ✗
Each H₂SO₄ gives two H⁺, so those 8.00 mmol OH⁻ neutralized only half as many acid units. ✗
Dr. Karmach

Worked example 2: the mole ratio

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄

Step 2 · Apply the mole ratio Step 3 · Divide to finish

The ratio, 1 H₂SO₄ per 2 NaOH, halves the count; the acid's volume then divides:

32.00 mL base × 0.250 mmol NaOH1 mL base × 1 mmol H₂SO₄2 mmol NaOH = 4.00 mmol H₂SO₄, then ÷ 20.00 mL acid = 0.200 M H₂SO₄
Dr. Karmach

Worked example 2: the mole ratio

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄
Step 2 · Apply the mole ratio Step 3 · Divide to finish
32.00 mL base × 0.250 mmol NaOH1 mL base × 1 mmol H₂SO₄2 mmol NaOH = 4.00 mmol H₂SO₄, then ÷ 20.00 mL acid = 0.200 M H₂SO₄
The 2:1 ratio halves the acid's millimoles, so its concentration is half the shortcut's guess: 0.200 M, not 0.400 M ✓
Dr. Karmach

Worked example 2: the route on the map

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 32.00 mL of 0.250 M NaOH · 20.00 mL H₂SO₄ · found: 0.200 M H₂SO₄

The same route as a 1 : 1 titration. Only the ratio step changes: 1 H₂SO₄ per 2 NaOH halves 8.00 mmol to 4.00 mmol. ✓
Dr. Karmach

Take-home: a polyprotic acid is not 1:1

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 32.00 mL of 0.250 M NaOH · 20.00 mL H₂SO₄
M = 8.00 mmol NaOH20.00 mL acid = 0.400 M ✗ · counts each H₂SO₄ as one H⁺
32.00 mL base × 0.250 mmol NaOH1 mL base × 1 mmol H₂SO₄2 mmol NaOH ÷ 20.00 mL acid = 0.200 M ✓

A diprotic acid feeds two H⁺, a triprotic three. The balanced equation's ratio divides the base's millimoles before the volume does. Skip it and every diprotic answer comes out doubled.

Dr. Karmach

Your turn: sulfuric acid and KOH

H₂SO₄ + 2 KOH → K₂SO₄ + 2 H₂O
given: 40.00 mL of 0.150 M KOH · 25.00 mL H₂SO₄ · wanted: M of the H₂SO₄

It takes 40.00 mL of 0.150 M KOH to titrate 25.00 mL of H₂SO₄. Fill the molarity, the 2:1 ratio, and the acid's volume, then compute:

40.00 mL base × mmol KOH1 mL base × 1 mmol H₂SO₄ mmol KOH = mmol H₂SO₄, then ÷ mL acid = M
Dr. Karmach

Your turn: sulfuric acid and KOH

H₂SO₄ + 2 KOH → K₂SO₄ + 2 H₂O
given: 40.00 mL of 0.150 M KOH · 25.00 mL H₂SO₄ · wanted: M of the H₂SO₄

It takes 40.00 mL of 0.150 M KOH to titrate 25.00 mL of H₂SO₄. Fill the molarity, the 2:1 ratio, and the acid's volume, then compute:

40.00 mL base × mmol KOH1 mL base × 1 mmol H₂SO₄ mmol KOH = mmol H₂SO₄, then ÷ mL acid = M
40.00 mL base × 0.150 mmol KOH1 mL base × 1 mmol H₂SO₄2 mmol KOH = 3.00 mmol H₂SO₄, then ÷ 25.00 mL acid = 0.120 M H₂SO₄
Dr. Karmach

Where this goes wrong

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 32.00 mL of 0.250 M NaOH · 20.00 mL H₂SO₄ · correct: 8.00 mmol NaOH → 4.00 mmol H₂SO₄ → 0.200 M
Treating the diprotic acid as 1:1. 8.00 mmol ÷ 20.00 mL = 0.400 M, double the truth. Each H₂SO₄ gives two H⁺, so divide the base's millimoles by 2 first.
Multiplying by the ratio instead of dividing. 2 × 8.00 ÷ 20.00 = 0.800 M. Each acid unit uses up two OH⁻, so there are fewer acid units than base units: the 2 divides.
Swapping the two volumes. Pairing 0.250 M with 20.00 mL gives 0.250 × 20.00 ÷ 2 ÷ 32.00 = 0.0781 M. Each molarity multiplies its own solution's volume.
Dr. Karmach

Practice 1

H₂C₂O₄ + 2 NaOH → Na₂C₂O₄ + 2 H₂O
titrant 0.125 M NaOH · sample 18.00 mL oxalic acid

It takes 28.80 mL of 0.125 M NaOH to reach the color change while titrating 18.00 mL of oxalic acid. What is the molarity of the oxalic acid?

  1. 1.80
  2. 0.100
  3. 0.200
  4. 0.400
Dr. Karmach

Practice 1 answer: B

H₂C₂O₄ + 2 NaOH → Na₂C₂O₄ + 2 H₂O
given: 18.00 mL H₂C₂O₄ · 28.80 mL of 0.125 M NaOH · wanted: M of the H₂C₂O₄
28.80 mL base × 0.125 mmol NaOH1 mL base × 1 mmol H₂C₂O₄2 mmol NaOH = 1.80 mmol H₂C₂O₄, then ÷ 18.00 mL acid = 0.100 M · answer B

A stopped at 1.80 mmol of oxalic acid, before dividing by its 18.00 mL. C ignored the 2:1 ratio: 3.60 ÷ 18.00 = 0.200 M. D multiplied by the ratio: 2 × 3.60 ÷ 18.00 = 0.400 M.

Two NaOH per oxalic acid, so the acid holds half the base's 3.60 mmol: 1.80 mmol in 18.00 mL is 0.100 M ✓
Dr. Karmach

Worked example 3: volume of base for a triprotic acid

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · titrant 0.150 M NaOH · wanted: mL of NaOH

A 25.00 mL sample of 0.0600 M phosphoric acid is titrated with 0.150 M NaOH. Phosphoric acid is triprotic: each unit gives three H⁺. What volume of base reaches the color change?

A common first attempt divides by 3 out of habit. Test it against the protons.

Dr. Karmach

Worked example 3: solution

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · wanted: mL of NaOH

This time the acid is the known solution, and the base's volume is the unknown.

Step 1 · Moles of the known solution

25.00 mL of 0.0600 M H₃PO₄ holds 25.00 × 0.0600 = 1.50 mmol H₃PO₄.

Dr. Karmach

Worked example 3: solution

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · wanted: mL of NaOH
Step 1 · Moles of the known solution A common first attempt
1.50 mmol ÷ 3 = 0.500 mmol NaOH → 0.500 ÷ 0.150 = 3.33 mL ✗
Each H₃PO₄ carries three H⁺, and each H⁺ takes one OH⁻. The base's millimoles are three times the acid's, not a third. ✗
Dr. Karmach

Worked example 3: the mole ratio

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · wanted: mL of NaOH

Step 2 · Apply the mole ratio Step 3 · Divide to finish

The ratio, 3 NaOH per H₃PO₄, triples the count; the base's molarity, upside down, turns millimoles into milliliters:

1.50 mmol H₃PO₄ × 3 mmol NaOH1 mmol H₃PO₄ × 1 mL base0.150 mmol NaOH = 30.0 mL NaOH
Dr. Karmach

Worked example 3: the mole ratio

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · wanted: mL of NaOH
Step 2 · Apply the mole ratio Step 3 · Divide to finish
1.50 mmol H₃PO₄ × 3 mmol NaOH1 mmol H₃PO₄ × 1 mL base0.150 mmol NaOH = 30.0 mL NaOH
4.50 mmol of NaOH at 0.150 mmol per mL takes 30.0 mL, nine times the 3.33 mL guess ✓
Dr. Karmach

Worked example 3: the route on the map

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · found: 30.0 mL NaOH

The acid is the known solution. The ratio triples 1.50 mmol to 4.50 mmol NaOH, and the volume exit divides by the base's 0.150 M. ✓
Dr. Karmach

Practice 2

H₃C₆H₅O₇ + 3 NaOH → Na₃C₆H₅O₇ + 3 H₂O
given: 26.40 mL of 0.120 M NaOH · citric acid 192.12 g/mol · wanted: g of citric acid

A powdered drink mix is dissolved in water, and its citric acid takes 26.40 mL of 0.120 M NaOH to reach the color change. How many grams of citric acid did the sample hold?

  1. 0.203
  2. 0.609
  3. 1.06
  4. 203
  5. 1.83
Dr. Karmach

Practice 2 answer: A

H₃C₆H₅O₇ + 3 NaOH → Na₃C₆H₅O₇ + 3 H₂O
26.40 mL of 0.120 M NaOH · citric acid 192.12 g/mol
26.40 mL base × 0.120 mmol NaOH1 mL base × 1 mmol acid3 mmol NaOH = 1.056 mmol acid
Dr. Karmach

Practice 2 answer: A

H₃C₆H₅O₇ + 3 NaOH → Na₃C₆H₅O₇ + 3 H₂O
26.40 mL of 0.120 M NaOH · citric acid 192.12 g/mol
26.40 mL base × 0.120 mmol NaOH1 mL base × 1 mmol acid3 mmol NaOH = 1.056 mmol acid
1.056 mmol × 1 mol1000 mmol × 192.12 g1 mol = 0.203 g · answer A

B ignored the 3:1 ratio: 3.168 mmol → 0.609 g. C stopped at 1.06 mmol, before the molar mass. D skipped mmol → mol: 1.056 × 192.12 = 203 g. E multiplied by the ratio: 9.504 mmol → 1.83 g.

1.056 mmol is a third of 3.168: three NaOH per citric acid. 203 g would outweigh the sample. ✓
Dr. Karmach

Check yourself

  1. A 1:1 titration takes 24.0 mL of 0.150 M NaOH to neutralize 20.0 mL of HCl. Set up Macid = Mbase · Vbase ÷ Vacid and find the HCl concentration.
  2. Phosphoric acid reacts as H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O. Which number becomes the base-to-acid ratio in the denominator, and where does it come from?

Every calculation here counted moles with a concentration, then crossed substances with the balanced equation's ratio: the same mole-ratio bridge that drives reaction stoichiometry. A concentration is only another way to count the moles a reaction runs on.

Dr. Karmach

Can you…?

  • ☐ explain "like dissolves like" and predict whether a solute dissolves in a given solvent?
  • ☐ describe unsaturated, saturated, and supersaturated solutions; read a solubility curve?
  • ☐ use the dilution relation M₁V₁ = M₂V₂ to find a concentration or volume?
  • ☐ calculate molality and mole fraction, and convert among molarity, molality, and mass percent?
  • ☐ classify a mixture as a solution, a colloid, or a suspension from particle size, light scattering, and settling, and name a colloid's type from its dispersed phase and medium?
  • ☐ apply colligative properties (freezing-point depression, boiling-point elevation, and Raoult's law) using the van't Hoff factor?
  • ☐ apply Henry's law to gas solubility and titration stoichiometry to find an unknown concentration?

If any box stays empty, the practice site has a drill for it. 🧪

Dr. Karmach