Solutions

Preparation for General Chemistry · Dr. Karmach

Dr. Karmach

By the end of this unit, you can…

  • Identify solute and solvent, write dissolving equations, and predict solubility with like dissolves like
  • Explain the dissolving process through the attractions broken and formed, and why dissolving can cool or warm the solution
  • Classify a solution as unsaturated, saturated, or supersaturated and predict how temperature and pressure (Henry's law) change solubility
  • Calculate and use molarity, percent concentration, ppm/ppb, and molality, and dilute a solution with M₁V₁ = M₂V₂
  • Carry a solution's volume and molarity through reaction stoichiometry
  • Describe the colligative properties and calculate freezing-point depression and boiling-point elevation with ΔT = i·K·m
Dr. Karmach

Today's route 🗺️

  1. Molarity
  2. Dilution
  3. Like Dissolves Like
  4. Saturation & Solubility Curves
  5. Henry's Law
  6. Percent Concentration
  7. Molality & Mole Fraction
  8. Freezing Point & Boiling Point
  9. Parts per Million & Parts per Billion
  10. Solution Stoichiometry
Dr. Karmach

1 · Molarity

Calculate the molarity of a solution from the amount of solute and the volume of solution, and use it as a conversion factor between solution volume and moles of solute, including the grams to weigh out to prepare a solution.

Dr. Karmach

Same mix, different strength

One spoonful of drink mix in a small glass tastes strong. The same spoonful in a full pitcher barely tastes at all. Only the water changed.

Dr. Karmach

Amount per liter, not total amount

Spread the same twelve particles through four liters instead of one, and each liter holds three. Taste, color, dose, and reactivity follow the amount in each liter, not the total.

Dr. Karmach

Solute, solvent, solution

solute + solvent → solution
dissolved substance · dissolving medium · uniform mixture

Sugar stirred into water spreads evenly through it. The sugar is the solute, the water the solvent, and the mixture a solution. Concentration states how much solute each volume of solution carries.

Dr. Karmach

Comparing three solutions

Concentration compares the amount of solute to the amount of solution. Rank the three copper(II) sulfate solutions: which is most concentrated, and which is most dilute?

Dr. Karmach

Comparing three solutions

Concentration compares the amount of solute to the amount of solution. Rank the three copper(II) sulfate solutions: which is most concentrated, and which is most dilute?

mol ÷ L:  A 0.40 ÷ 1.0 = 0.40 · B 0.40 ÷ 2.0 = 0.20 · C 0.20 ÷ 0.25 = 0.80
most concentrated: C · most dilute: B · C holds the least CuSO₄ in total but the most in each liter
Dr. Karmach

Molarity: moles per liter of solution

M = mol solute ÷ L solution
6.0 M HCl: every liter of the solution carries 6.0 mol HCl · read "six molar"

Molarity, symbol M, counts the moles of solute in each liter of solution: a rate, not a total. Reactions consume particles, not grams; two solutions at the same g/L can carry different particle counts.

Dr. Karmach

Liters of solution, not water added

The solute takes up room. Prepare the solution in a volumetric flask: solute in first, then water to the mark. The mark reads the volume of finished solution, solute included.

Dr. Karmach

The method

  1. Grams → moles: convert the solute's mass with its molar mass.
  2. mL → L: molarity counts liters of solution.
  3. Divide moles by liters: the quotient is the molarity, in mol/L.
Dr. Karmach

The molarity map

Divide moles by liters to find a molarity. Once known, the molarity converts between moles of solute and liters of solution. The molar mass reaches grams.

Dr. Karmach

Guided example: a sports drink

M = mol solute ÷ L solution
given: 0.300 mol glucose · 1.50 L of solution · wanted: M

A sports drink is mixed so that 1.50 L of it holds 0.300 mol of glucose. What is its molarity?

Check each given against the three method steps, then divide.

Dr. Karmach

Guided example: solution

M = mol solute ÷ L solution
given: 0.300 mol glucose · 1.50 L of solution · wanted: M

Step 1 · Grams → moles

The amount is already in moles: 0.300 mol glucose. No molar mass is needed.

Dr. Karmach

Guided example: solution

M = mol solute ÷ L solution
given: 0.300 mol glucose · 1.50 L of solution · wanted: M
Step 1 · Grams → moles Step 2 · mL → L

The volume is already in liters: 1.50 L of solution.

Dr. Karmach

Guided example: solution

M = mol solute ÷ L solution
given: 0.300 mol glucose · 1.50 L of solution · wanted: M
Step 1 · Grams → moles Step 2 · mL → L Step 3 · Divide moles by liters
M = 0.300 mol glucose1.50 L soln = 0.200 M glucose
Dr. Karmach

Guided example: solution

M = mol solute ÷ L solution
given: 0.300 mol glucose · 1.50 L of solution · wanted: M
Step 1 · Grams → moles Step 2 · mL → L Step 3 · Divide moles by liters
M = 0.300 mol glucose1.50 L soln = 0.200 M glucose
1.50 L holds 0.300 mol, so each half liter holds 0.100 mol and a full liter holds 0.200 mol. 0.200 M ✓
Dr. Karmach

Guided example: the route on the map

M = mol solute ÷ L solution
given: 0.300 mol glucose · 1.50 L of solution · found: 0.200 M glucose

Moles and liters were both in hand, so the route is one move: moles on top, liters on the bottom. ✓
Dr. Karmach

Practice 1

M = mol solute ÷ L solution
measured: 0.270 mol sucrose · 1.15 L of water · 1.20 L after dissolving

A student stirs 0.270 mol of sucrose into 1.15 L of water. Once it dissolves, the solution measures 1.20 L. What is the molarity of the sucrose solution?

  1. 0.235
  2. 4.44
  3. 0.324
  4. 0.225
Dr. Karmach

Practice 1: answer D

M = mol solute ÷ L solution
0.270 mol sucrose · 1.20 L of solution · the 1.15 L of water is not the solution volume
M = 0.270 mol sucrose1.20 L soln = 0.225 M sucrose (answer D)

A divided by the water added: 0.270 ÷ 1.15 = 0.235, but the dissolved sugar takes up room too. B flipped the fraction: 1.20 ÷ 0.270 = 4.44, in L/mol. C multiplied: 0.270 × 1.20 = 0.324, in mol·L.

A bit more than a liter holds 0.270 mol, so one liter holds a bit less: 0.225 < 0.270 ✓
Dr. Karmach

Worked example 1: molarity from moles and volume

M = mol solute ÷ L solution
given: 0.350 mol NaCl · 500.0 mL of solution · wanted: M

A stockroom bottle is prepared with 0.350 mol of NaCl dissolved in enough water to make 500.0 mL of solution. Find the molarity for the label.

Set it up: get the volume into liters, then divide.

Dr. Karmach

Worked example 1: solution

M = mol solute ÷ L solution
given: 0.350 mol NaCl · 500.0 mL of solution · wanted: M

Step 1 · Grams → moles

The mole count is given directly: 0.350 mol NaCl, no mass conversion needed.

Dr. Karmach

Worked example 1: solution

M = mol solute ÷ L solution
given: 0.350 mol NaCl · 500.0 mL of solution · wanted: M
Step 1 · Grams → moles Step 2 · mL → L
500.0 mL = 0.5000 L
1000 mL = 1 L · the definition counts liters of solution
Dr. Karmach

Worked example 1: solution

M = mol solute ÷ L solution
given: 0.350 mol NaCl · 500.0 mL of solution · wanted: M
Step 1 · Grams → moles Step 2 · mL → L
500.0 mL = 0.5000 L
1000 mL = 1 L · the definition counts liters of solution
Step 3 · Divide moles by liters
M = 0.350 mol NaCl0.5000 L soln = 0.700 M NaCl
Dr. Karmach

Worked example 1: solution

M = mol solute ÷ L solution
given: 0.350 mol NaCl · 500.0 mL of solution · wanted: M
Step 1 · Grams → moles Step 2 · mL → L
500.0 mL = 0.5000 L
1000 mL = 1 L · the definition counts liters of solution
Step 3 · Divide moles by liters
M = 0.350 mol NaCl0.5000 L soln = 0.700 M NaCl
Half a liter carries 0.350 mol, so a full liter carries twice that: 0.700 mol. 0.700 M ✓
Dr. Karmach

Worked example 1: the route on the map

M = mol solute ÷ L solution
given: 0.350 mol NaCl · 500.0 mL of solution · found: 0.700 M NaCl

Two moves: 500.0 mL becomes 0.5000 L, then moles on top, liters on the bottom. ✓
Dr. Karmach

Worked example 2: molarity from grams

M = mol solute ÷ L solution
given: 9.35 g KCl · water to the 250.0 mL mark · molar mass KCl 74.55 g/mol

A student measures out 9.35 g of KCl (74.55 g/mol), transfers it to a volumetric flask, and adds water to the 250.0 mL mark. Find the molarity.

A common first attempt: divide the moles by 250. Test the units.

Dr. Karmach

Worked example 2: solution

M = mol solute ÷ L solution
given: 9.35 g KCl (74.55 g/mol) · water to the 250.0 mL mark · wanted: M

Step 1 · Grams → moles

The molar mass converts the mass to moles: 9.35 g ÷ 74.55 g/mol = 0.1254 mol KCl.

Dr. Karmach

Worked example 2: solution

M = mol solute ÷ L solution
given: 9.35 g KCl (74.55 g/mol) · water to the 250.0 mL mark · wanted: M
Step 1 · Grams → moles A common first attempt
M = 0.1254 mol KCl250 mL soln = 0.000502 mol/mL ✗

The unit came out mol/mL. Molarity is mol/L: the volume must enter in liters.

Dr. Karmach

Worked example 2: solution

M = mol solute ÷ L solution
given: 9.35 g KCl (74.55 g/mol) · water to the 250.0 mL mark · wanted: M
Step 1 · Grams → moles A common first attempt
M = 0.1254 mol KCl250 mL soln = 0.000502 mol/mL ✗
Step 2 · mL → L Step 3 · Divide moles by liters

The mark reads 250.0 mL of solution, which is 0.2500 L. Divide:

9.35 g KCl × 1 mol KCl74.55 g KCl = 0.1254 mol, then 0.1254 mol KCl0.2500 L soln = 0.502 M KCl
Dr. Karmach

Worked example 2: solution

M = mol solute ÷ L solution
given: 9.35 g KCl (74.55 g/mol) · water to the 250.0 mL mark · wanted: M
Step 1 · Grams → moles A common first attempt
M = 0.1254 mol KCl250 mL soln = 0.000502 mol/mL ✗
Step 2 · mL → L Step 3 · Divide moles by liters
9.35 g KCl × 1 mol KCl74.55 g KCl = 0.1254 mol, then 0.1254 mol KCl0.2500 L soln = 0.502 M KCl
A quarter liter carries 0.1254 mol, so a full liter carries four times that: 0.502 mol. 0.502 M ✓
Dr. Karmach

Worked example 2: the route on the map

M = mol solute ÷ L solution
given: 9.35 g KCl (74.55 g/mol) · 250.0 mL of solution · found: 0.502 M KCl

Three moves: the molar mass turns grams into moles, 250.0 mL becomes 0.2500 L, then divide. ✓
Dr. Karmach

Your turn: sodium carbonate

M = mol solute ÷ L solution
given: 21.2 g Na₂CO₃ (105.99 g/mol) · water to the 500.0 mL mark · wanted: M

A wash solution is prepared: 21.2 g of Na₂CO₃ (105.99 g/mol) in a volumetric flask, water to the 500.0 mL mark.

21.2 g Na₂CO₃ × 1 mol Na₂CO₃ g Na₂CO₃ = mol, then mol Na₂CO₃ L soln = M

Fill the molar mass, the moles, and the liters, then compute the molarity.

Dr. Karmach

Your turn: sodium carbonate

M = mol solute ÷ L solution
given: 21.2 g Na₂CO₃ (105.99 g/mol) · water to the 500.0 mL mark · wanted: M

A wash solution is prepared: 21.2 g of Na₂CO₃ (105.99 g/mol) in a volumetric flask, water to the 500.0 mL mark.

21.2 g Na₂CO₃ × 1 mol Na₂CO₃ g Na₂CO₃ = mol, then mol Na₂CO₃ L soln = M

Fill the molar mass, the moles, and the liters, then compute the molarity.

21.2 g Na₂CO₃ × 1 mol Na₂CO₃105.99 g Na₂CO₃ = 0.200 mol, then 0.200 mol Na₂CO₃0.5000 L soln = 0.400 M Na₂CO₃
Dr. Karmach

Where this goes wrong

9.35 g KCl (74.55 g/mol) · water to the 250.0 mL mark
correct: 9.35 g → 0.1254 mol · 250.0 mL → 0.2500 L · M = 0.502 M
Dividing by milliliters. 0.1254 mol ÷ 250 mL = 0.000502, and the unit is mol/mL, 1000 times too small. Molarity divides by liters of solution: 0.1254 ÷ 0.2500 = 0.502 M.
Dividing grams by liters. 9.35 ÷ 0.2500 = 37.4 is a mass concentration in g/L, not a molarity. Molarity counts moles of solute: 9.35 g ÷ 74.55 g/mol = 0.1254 mol first.
Multiplying by the molar mass. 9.35 × 74.55 = 697 carries units of g²/mol, which is not a mole count. Grams → moles divides by the molar mass: 9.35 ÷ 74.55 = 0.1254 mol.
Dr. Karmach

Practice 2

M = mol solute ÷ L solution
molar mass KNO₃ 101.11 g/mol

What is the molarity of 225 mL of a potassium nitrate solution that contains 34.8 g of KNO₃?

  1. 0.344
  2. 1.53
  3. 0.00153
  4. 15.5
  5. 155
Dr. Karmach

Practice 2: answer B

M = mol solute ÷ L solution
34.8 g KNO₃ (101.11 g/mol) · 225 mL of solution = 0.225 L · wanted: M
34.8 g KNO₃ × 1 mol KNO₃101.11 g KNO₃ = 0.344 mol, then 0.344 mol KNO₃0.225 L soln = 1.53 M KNO₃ (answer B)

A stopped at moles: 34.8 ÷ 101.11 = 0.344 mol is the amount in the sample. C divided by milliliters: 0.344 ÷ 225 = 0.00153, in mol/mL. D found the percent: 34.8 ÷ 225 × 100 = 15.5% (m/v). E divided grams by liters: 34.8 ÷ 0.225 = 155 g/L.

A bit under a quarter liter carries 0.344 mol, so a full liter carries a bit over four times that, over 1.38 mol. 1.53 M ✓
Dr. Karmach

Practice 3

M = mol solute ÷ L solution
measured: 2.000 L batch · 25.00 mL portion dried · 2.38 g KBr residue · molar mass KBr 119.00 g/mol

A technician prepares a 2.000 L batch of KBr solution. A 25.00 mL portion of it is evaporated to dryness, and the residue weighs 2.38 g. What is the molarity of the batch?

  1. 0.800
  2. 0.0100
  3. 0.0200
  4. 0.000800
  5. 0.000500
Dr. Karmach

Practice 3: answer A

M = mol solute ÷ L solution
25.00 mL portion = 0.02500 L · 2.38 g KBr (119.00 g/mol) in it · the portion has the batch's molarity
2.38 g KBr × 1 mol KBr119.00 g KBr = 0.0200 mol, then 0.0200 mol KBr0.02500 L soln = 0.800 M KBr (answer A)

B divided by the whole batch: 0.0200 ÷ 2.000 = 0.0100, but the 2.38 g came from only 25.00 mL. C stopped at moles: 0.0200 mol is the amount in the portion. D divided by milliliters: 0.0200 ÷ 25.00 = 0.000800, in mol/mL. E multiplied by the volume instead of dividing: 0.0200 × 0.02500 = 0.000500.

A uniform solution has the same molarity in every portion. A fortieth of a liter carries 0.0200 mol, so a full liter carries forty times that: 0.800 mol. 0.800 M ✓
Dr. Karmach

A molarity is an equality

0.450 mol KOH = 1 L of solution
the label "0.450 M KOH" states this equality

Every equality gives a conversion factor. This one converts between volume of solution and moles of solute:

0.450 mol KOH1 L soln or 1 L soln0.450 mol KOH

Write it so the given unit cancels.

Dr. Karmach

Worked example 3: liters from grams

3.00 mol NaCl = 1 L of solution
given: 351 g NaCl (58.44 g/mol) · 3.00 M NaCl · wanted: L of solution · route: g → mol → L

How many liters of 3.00 M NaCl solution can be made from 351 g of NaCl?

Count the factors on the route: g → mol → L.

Dr. Karmach

Worked example 3: solution

3.00 mol NaCl = 1 L of solution
given: 351 g NaCl (58.44 g/mol) · wanted: L of solution · route: g → mol → L

Two conversion factors are needed.

Step 1 · Grams → moles

351 g NaCl × 1 mol NaCl58.44 g NaCl = 6.01 mol NaCl
Dr. Karmach

Worked example 3: solution

3.00 mol NaCl = 1 L of solution
given: 351 g NaCl (58.44 g/mol) · wanted: L of solution · route: g → mol → L
Step 1 · Grams → moles
351 g NaCl × 1 mol NaCl58.44 g NaCl = 6.01 mol NaCl
Write the molarity fraction

Two orientations exist. Only one cancels mol NaCl:

1 L soln3.00 mol NaCl cancels mol NaCl ✓    3.00 mol NaCl1 L soln cancels nothing ✗
Dr. Karmach

Worked example 3: solution

3.00 mol NaCl = 1 L of solution
given: 351 g NaCl (58.44 g/mol) · wanted: L of solution · route: g → mol → L
Step 1 · Grams → moles
351 g NaCl × 1 mol NaCl58.44 g NaCl = 6.01 mol NaCl
Write the molarity fraction Multiply and check
351 g NaCl × 1 mol NaCl58.44 g NaCl × 1 L soln3.00 mol NaCl = 2.00 L soln
Dr. Karmach

Worked example 3: solution

3.00 mol NaCl = 1 L of solution
given: 351 g NaCl (58.44 g/mol) · wanted: L of solution · route: g → mol → L
Step 1 · Grams → moles
351 g NaCl × 1 mol NaCl58.44 g NaCl = 6.01 mol NaCl
Write the molarity fraction Multiply and check
351 g NaCl × 1 mol NaCl58.44 g NaCl × 1 L soln3.00 mol NaCl = 2.00 L soln
Each liter carries 3.00 mol, and 351 g is 6.01 mol: two liters' worth. 2.00 L ✓
Dr. Karmach

Worked example 3: the route on the map

3.00 mol NaCl = 1 L of solution
given: 351 g NaCl · 3.00 M NaCl · found: 2.00 L of solution

Two moves: the molar mass reaches moles, then the molarity, liters over moles, reaches liters. ✓
Dr. Karmach

Worked example 4: volume from mass of solute

0.450 mol KOH = 1 L of solution
given: 15.1 g KOH (56.11 g/mol) · wanted: mL of solution · route: g → mol → L → mL

A procedure calls for 15.1 g of KOH, and the shelf stocks 0.450 M KOH solution. What volume of that solution, in milliliters, delivers the 15.1 g?

Count the factors on the route: g → mol → L → mL.

Dr. Karmach

Worked example 4: solution

0.450 mol KOH = 1 L of solution
given: 15.1 g KOH (56.11 g/mol) · wanted: mL of solution · route: g → mol → L → mL

Three conversion factors are needed.

Step 1 · Grams → moles

15.1 g KOH × 1 mol KOH56.11 g KOH = 0.269 mol KOH
Dr. Karmach

Worked example 4: solution

0.450 mol KOH = 1 L of solution
given: 15.1 g KOH (56.11 g/mol) · wanted: mL of solution · route: g → mol → L → mL
Step 1 · Grams → moles
15.1 g KOH × 1 mol KOH56.11 g KOH = 0.269 mol KOH
Multiply and check
15.1 g KOH × 1 mol KOH56.11 g KOH × 1 L soln0.450 mol KOH × 1000 mL soln1 L soln = 598 mL soln
Dr. Karmach

Worked example 4: solution

0.450 mol KOH = 1 L of solution
given: 15.1 g KOH (56.11 g/mol) · wanted: mL of solution · route: g → mol → L → mL
Step 1 · Grams → moles
15.1 g KOH × 1 mol KOH56.11 g KOH = 0.269 mol KOH
Multiply and check
15.1 g KOH × 1 mol KOH56.11 g KOH × 1 L soln0.450 mol KOH × 1000 mL soln1 L soln = 598 mL soln
Each liter carries 0.450 mol, and 0.269 mol is wanted, a bit over half a liter: 598 mL ✓
Dr. Karmach

Worked example 4: the route on the map

0.450 mol KOH = 1 L of solution
given: 15.1 g KOH · 0.450 M KOH · found: 598 mL of solution

One move past liters: 1 L = 1000 mL turns 0.598 L into 598 mL. ✓
Dr. Karmach

Practice 4

0.400 mol KNO₃ = 1 L of solution
the label "0.400 M KNO₃" states this equality · molar mass KNO₃ 101.11 g/mol

A greenhouse feed calls for 10.1 g of KNO₃, supplied as 0.400 M KNO₃ solution. What volume, in milliliters, carries that mass?

  1. 0.250
  2. 40.0
  3. 0.0999
  4. 250.
Dr. Karmach

Practice 4: answer D

0.400 mol KNO₃ = 1 L of solution
given: 10.1 g KNO₃ (101.11 g/mol) · wanted: mL of solution · route: g → mol → L → mL
10.1 g KNO₃ × 1 mol KNO₃101.11 g KNO₃ × 1 L soln0.400 mol KNO₃ × 1000 mL soln1 L soln = 250. mL (answer D)

A stopped at liters and relabeled: 10.1 ÷ 101.11 ÷ 0.400 = 0.250 L, which is 250. mL, not 0.250 mL. B flipped the molarity fraction: 10.1 ÷ 101.11 × 0.400 × 1000 = 40.0, and the units, mol²/L, are not a volume. C stopped at moles: 10.1 ÷ 101.11 = 0.0999 mol is the KNO₃ needed, not the volume that carries it.

Each liter carries 0.400 mol, and the target is 0.0999 mol, a quarter of a liter: 250. mL ✓
Dr. Karmach

Worked example 5: preparing a solution from the solid

0.10 mol NaOH = 1 L of solution
given: 1.0 L of 0.10 M NaOH to prepare · NaOH 40.00 g/mol · wanted: g NaOH, then the steps

Describe how to prepare 1.0 L of 0.10 M NaOH from solid NaOH.

Find the mass first. Count the factors on the route: L → mol → g.

Dr. Karmach

Worked example 5: solution

0.10 mol NaOH = 1 L of solution
given: 1.0 L of 0.10 M NaOH (40.00 g/mol) · wanted: g NaOH · route: L → mol → g

Two conversion factors are needed.

Liters → moles: the molarity

1.0 L soln × 0.10 mol NaOH1 L soln = 0.10 mol NaOH
Dr. Karmach

Worked example 5: solution

0.10 mol NaOH = 1 L of solution
given: 1.0 L of 0.10 M NaOH (40.00 g/mol) · wanted: g NaOH · route: L → mol → g
Liters → moles: the molarity
1.0 L soln × 0.10 mol NaOH1 L soln = 0.10 mol NaOH
Moles → grams: the molar mass
1.0 L soln × 0.10 mol NaOH1 L soln × 40.00 g NaOH1 mol NaOH = 4.0 g NaOH
Dr. Karmach

Worked example 5: solution

0.10 mol NaOH = 1 L of solution
given: 1.0 L of 0.10 M NaOH (40.00 g/mol) · wanted: g NaOH · route: L → mol → g
Liters → moles: the molarity
1.0 L soln × 0.10 mol NaOH1 L soln = 0.10 mol NaOH
Moles → grams: the molar mass
1.0 L soln × 0.10 mol NaOH1 L soln × 40.00 g NaOH1 mol NaOH = 4.0 g NaOH
A liter of 0.10 M holds 0.10 mol, a tenth of a mole: a tenth of 40.00 g is 4.0 g ✓
Dr. Karmach

Worked example 5: the route on the map

0.10 mol NaOH = 1 L of solution
given: 1.0 L of 0.10 M NaOH · found: 4.0 g NaOH

Liters in, grams out: the molarity reaches moles, then the molar mass reaches grams. ✓
Dr. Karmach

Worked example 5: making the solution

0.10 mol NaOH = 1 L of solution
found: 4.0 g NaOH · flask: 1.0 L volumetric

Weigh 4.0 g of NaOH. Dissolve it in part of the water in a 1.0 L volumetric flask. Add water to the mark, then mix.

Dr. Karmach

Worked example 5: making the solution

0.10 mol NaOH = 1 L of solution
found: 4.0 g NaOH · flask: 1.0 L volumetric

Weigh 4.0 g of NaOH. Dissolve it in part of the water in a 1.0 L volumetric flask. Add water to the mark, then mix.

The mark measures 1.0 L of solution, not 1.0 L of water added. ✓
Dr. Karmach

Practice 5

0.150 mol Na₂SO₄ = 1 L of solution
molar mass Na₂SO₄ 142.04 g/mol

A dye bath calls for 500.0 mL of 0.150 M Na₂SO₄. What mass of Na₂SO₄, in grams, must be dissolved to make it?

  1. 21.3
  2. 10.7
  3. 473
  4. 1.07 × 10⁴
Dr. Karmach

Practice 5: answer B

0.150 mol Na₂SO₄ = 1 L of solution
given: 500.0 mL of 0.150 M Na₂SO₄ (142.04 g/mol) · wanted: g Na₂SO₄ · route: mL → L → mol → g
500.0 mL soln × 1 L soln1000 mL soln × 0.150 mol Na₂SO₄1 L soln × 142.04 g Na₂SO₄1 mol Na₂SO₄ = 10.7 g (answer B)

A left out the volume: 0.150 × 142.04 = 21.3 g is the mass in a full liter. C flipped the molarity: 0.5000 ÷ 0.150 × 142.04 = 473, and the units do not cancel. D skipped mL → L: 500.0 × 0.150 × 142.04 = 1.07 × 10⁴.

Half a liter of 0.150 M holds 0.0750 mol, at about 142 g per mole: about 11 g. 10.7 g ✓
Dr. Karmach

Worked example 6: ethanol in blood

0.080 mol C₂H₆O = 1 L of solution
given: 5.6 L of blood at 0.080 M ethanol · C₂H₆O 46.07 g/mol · wanted: g ethanol, then % (m/v)

A blood level of 0.080 M ethanol (C₂H₆O) can induce a coma. What total mass of ethanol is in an adult with 5.6 L of blood at this level? What is the blood alcohol level in % (m/v)?

Find the mass first. Count the factors on the route: L → mol → g.

Dr. Karmach

Worked example 6: solution

0.080 mol C₂H₆O = 1 L of solution
given: 5.6 L of blood at 0.080 M (46.07 g/mol) · wanted: g C₂H₆O, then % (m/v)

Two conversion factors are needed for the mass.

Liters → moles: the molarity

5.6 L soln × 0.080 mol C₂H₆O1 L soln = 0.45 mol C₂H₆O
Dr. Karmach

Worked example 6: solution

0.080 mol C₂H₆O = 1 L of solution
given: 5.6 L of blood at 0.080 M (46.07 g/mol) · wanted: g C₂H₆O, then % (m/v)
Liters → moles: the molarity
5.6 L soln × 0.080 mol C₂H₆O1 L soln = 0.45 mol C₂H₆O
Moles → grams: the molar mass
5.6 L soln × 0.080 mol C₂H₆O1 L soln × 46.07 g C₂H₆O1 mol C₂H₆O = 21 g C₂H₆O
Dr. Karmach

Worked example 6: solution

0.080 mol C₂H₆O = 1 L of solution
given: 5.6 L of blood at 0.080 M (46.07 g/mol) · wanted: g C₂H₆O, then % (m/v)
Liters → moles: the molarity
5.6 L soln × 0.080 mol C₂H₆O1 L soln = 0.45 mol C₂H₆O
Moles → grams: the molar mass
5.6 L soln × 0.080 mol C₂H₆O1 L soln × 46.07 g C₂H₆O1 mol C₂H₆O = 21 g C₂H₆O
Each liter carries 0.080 mol, about 3.7 g, and 5.6 × 3.7 is about 21. 21 g ✓
Dr. Karmach

Worked example 6: the percent

0.080 mol C₂H₆O = 1 L of solution
found: 21 g C₂H₆O (20.6 unrounded) in 5.6 L of blood · wanted: % (m/v)

Grams per 100 mL: the % (m/v)

Keep the unrounded 20.6 g in the calculator. The blood is the solution: 5.6 L = 5.6 × 10³ mL.

Dr. Karmach

Worked example 6: the percent

0.080 mol C₂H₆O = 1 L of solution
found: 21 g C₂H₆O (20.6 unrounded) in 5.6 L of blood · wanted: % (m/v)

Grams per 100 mL: the % (m/v)

Keep the unrounded 20.6 g in the calculator. The blood is the solution: 5.6 L = 5.6 × 10³ mL.

20.6 g C₂H₆O5.6 × 10³ mL soln × 100 = 0.37% (m/v)
Dr. Karmach

Worked example 6: the percent

0.080 mol C₂H₆O = 1 L of solution
found: 21 g C₂H₆O (20.6 unrounded) in 5.6 L of blood · wanted: % (m/v)

Grams per 100 mL: the % (m/v)

Keep the unrounded 20.6 g in the calculator. The blood is the solution: 5.6 L = 5.6 × 10³ mL.

20.6 g C₂H₆O5.6 × 10³ mL soln × 100 = 0.37% (m/v)
Each liter carries about 3.7 g, so each 100 mL carries about 0.37 g: 0.37% (m/v) ✓
Dr. Karmach

Worked example 6: the route on the map

0.080 mol C₂H₆O = 1 L of solution
given: 5.6 L of blood at 0.080 M · found: 21 g C₂H₆O · 0.37% (m/v)

Molarity, then molar mass, reach grams. Liters become mL for the % (m/v). ✓
Dr. Karmach

Practice 6

0.200 mol CuSO₄ = 1 L of solution
the label "0.200 M CuSO₄" states this equality · molar mass CuSO₄ 159.61 g/mol

A teaching lab fills six volumetric flasks, each to its 250.0 mL line, with 0.200 M CuSO₄. What total mass of CuSO₄, in grams, must be weighed out?

  1. 7.98
  2. 1.20 × 10³
  3. 47.9
  4. 0.300
  5. 4.79 × 10⁴
Dr. Karmach

Practice 6: answer C

0.200 mol CuSO₄ = 1 L of solution
given: 6 × 250.0 mL = 1500. mL = 1.500 L of 0.200 M CuSO₄ (159.61 g/mol) · wanted: total g CuSO₄
1.500 L soln × 0.200 mol CuSO₄1 L soln × 159.61 g CuSO₄1 mol CuSO₄ = 47.9 g (answer C)

A filled one flask: 0.2500 × 0.200 × 159.61 = 7.98. B flipped the molarity: 1.500 ÷ 0.200 × 159.61 = 1.20 × 10³. D stopped at moles: 1.500 × 0.200 = 0.300 mol. E skipped mL → L: 1500. × 0.200 × 159.61 = 4.79 × 10⁴.

Six quarter liters make 1.500 L. That holds 0.300 mol, at about 160 g per mole: about 48 g. 47.9 g ✓
Dr. Karmach

Practice 6: the route on the map

0.200 mol CuSO₄ = 1 L of solution
given: six flasks of 250.0 mL · found: 47.9 g CuSO₄

Add the flask volumes first, 1500. mL, then make the three moves of a single flask. ✓
Dr. Karmach

2 · 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

A stock bottle skips the weighing

NaOH comes as a solid or a 10.0 M stock. Both fill the flask with 0.100 mol. Measuring some stock and adding water is a dilution: a weaker solution from a stronger one.

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

C₁V₁ = C₂V₂: any concentration unit

C₁V₁ = C₂V₂
C in M: M × L counts moles of solute · C in % (m/v): % × mL ÷ 100 counts grams of solute

Adding water changes neither the moles nor the grams of solute. The relation holds for molarity and percent (m/v) alike. C₁ and C₂ share one unit: M with M, % with %.

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 units: C₁ with C₂, V₁ with V₂.
  4. Substitute and solve; the diluted concentration comes out lower.

Dr. Karmach

Guided example: NaOH from the 10.0 M stock

M₁V₁ = M₂V₂
given: stock 10.0 M NaOH · target 0.200 M · final volume 250. mL · wanted: mL of stock

A lab needs 250. mL of 0.200 M NaOH. The shelf holds the 10.0 M NaOH stock. What volume of the stock, in mL, is measured out?

The stock bottle is "before". The finished flask is "after".

Dr. Karmach

Guided example: solution

M₁V₁ = M₂V₂
given: stock 10.0 M NaOH · target 0.200 M · final volume 250. mL · wanted: mL of stock

Step 1 · List the knowns

Before, the stock: M₁ = 10.0 M, and V₁ is the unknown. After, the flask: M₂ = 0.200 M and V₂ = 250. mL.

Dr. Karmach

Guided example: solution

M₁V₁ = M₂V₂
given: stock 10.0 M NaOH · target 0.200 M · final volume 250. mL · wanted: mL of stock
Step 1 · List the knowns Step 2 · Rearrange
M₁V₁ = M₂V₂ → V₁ = V₂ × M₂M₁
Dr. Karmach

Guided example: solution

M₁V₁ = M₂V₂
given: stock 10.0 M NaOH · target 0.200 M · final volume 250. mL · wanted: mL of stock
Step 1 · List the knowns Step 2 · Rearrange
M₁V₁ = M₂V₂ → V₁ = V₂ × M₂M₁
Step 3 · Match the units

Both concentrations are in M, so they cancel. V₂ is in mL, so V₁ comes out in mL.

Dr. Karmach

Guided example: solution

M₁V₁ = M₂V₂
given: stock 10.0 M NaOH · target 0.200 M · final volume 250. mL · wanted: mL of stock
Step 1 · List the knowns Step 2 · Rearrange
M₁V₁ = M₂V₂ → V₁ = V₂ × M₂M₁
Step 3 · Match the units Step 4 · Substitute and solve
V₁ = 250. mL × 0.200 M10.0 M = 5.00 mL

At the bench: measure 5.00 mL of the stock, then add water to the 250. mL mark.

Dr. Karmach

Guided example: solution

M₁V₁ = M₂V₂
given: stock 10.0 M NaOH · target 0.200 M · final volume 250. mL · wanted: mL of stock
Step 1 · List the knowns Step 2 · Rearrange
M₁V₁ = M₂V₂ → V₁ = V₂ × M₂M₁
Step 3 · Match the units Step 4 · Substitute and solve
V₁ = 250. mL × 0.200 M10.0 M = 5.00 mL
The stock is 50 times stronger, 10.0 M against 0.200 M, so it fills a fiftieth of the flask: 250. ÷ 50 = 5.00 mL ✓
Dr. Karmach

Guided example: the route on the map

M₁V₁ = M₂V₂
given: 10.0 M stock · 0.200 M target · 250. mL final · found: V₁ = 5.00 mL of stock

The unknown is the stock volume, so V₁ = V₂ × M₂ ÷ M₁. Both volumes are in mL, and no water amount was asked. ✓
Dr. Karmach

Practice 1

M₁V₁ = M₂V₂
stock 12.0 M HCl · target 0.600 M · batch 300. mL

A titration calls for 0.600 M HCl. How many milliliters of 12.0 M HCl stock go into a 300. mL batch?

  1. 6.00 × 10³
  2. 180.
  3. 285
  4. 15.0
Dr. Karmach

Practice 1 answer: D

M₁V₁ = M₂V₂
given: stock 12.0 M · target 0.600 M · 300. mL batch · wanted: mL of stock
V₁ = 300. mL × 0.600 M12.0 M = 15.0 mL · answer D

A flipped the ratio: 300. × (12.0 ÷ 0.600) = 6.00 × 10³ mL, twenty times the batch. B stopped at the solute: 300. × 0.600 = 180. mmol of HCl, not a volume. C reported the water: 300. − 15.0 = 285 mL goes in after the stock.

The stock is 20 times stronger, so it fills a twentieth of the batch: 300. ÷ 20 = 15.0 mL ✓
Dr. Karmach

Practice 1: the route on the map

M₁V₁ = M₂V₂
given: stock 12.0 M · target 0.600 M · 300. mL batch · found: V₁ = 15.0 mL of stock

The unknown is the stock volume, the path of the guided example: V₁ = V₂ × M₂ ÷ M₁. Both volumes are in mL. ✓
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 2

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 2 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

Practice 2: the route on the map

M₁V₁ = M₂V₂
given: 5.00 M · 40.0 mL HNO₃ · dilute to 0.400 M · found: 460. mL of water added

V₂ = V₁ × M₁ ÷ M₂ gives the total, 500. mL. The question asked for the water, so the last step subtracts the 40.0 mL of acid. ✓
Dr. Karmach

Worked example 3: a percent dilution

C₁V₁ = C₂V₂
given: 9.00% (m/v) NaOH · 10.0 mL stock · water to 60.0 mL final · wanted: % (m/v) after

A technician dilutes 10.0 mL of 9.00% (m/v) NaOH with water to a final volume of 60.0 mL. Find the new percent (m/v).

Percent is the concentration unit here. The steps do not change.

Dr. Karmach

Worked example 3: solution

C₁V₁ = C₂V₂
given: 9.00% (m/v) · 10.0 mL stock · water to 60.0 mL final · wanted: C₂ in % (m/v)

A common first attempt

C₂ = 9.00% × 10.0 mL50.0 mL water = 1.80% ✗

50.0 mL is only the water added. A percent counts per 100 mL of solution, and the solution is all 60.0 mL: stock plus water.

Dr. Karmach

Worked example 3: solution

C₁V₁ = C₂V₂
given: 9.00% (m/v) · 10.0 mL stock · water to 60.0 mL final · wanted: C₂ in % (m/v)
A common first attempt
C₂ = 9.00% × 10.0 mL50.0 mL water = 1.80% ✗
Step 1 · List the knowns

C₁ = 9.00% (m/v). V₁ = 10.0 mL. V₂ = 60.0 mL, the whole solution. The unknown is C₂.

Dr. Karmach

Worked example 3: solution

C₁V₁ = C₂V₂
given: 9.00% (m/v) · 10.0 mL stock · water to 60.0 mL final · wanted: C₂ in % (m/v)
A common first attempt
C₂ = 9.00% × 10.0 mL50.0 mL water = 1.80% ✗
Step 1 · List the knowns Step 2 · Rearrange Step 3 · Match the units

C₂ = C₁ × V₁ ÷ V₂. Both volumes are in mL, so C₂ comes out in % (m/v), the unit of C₁.

Dr. Karmach

Worked example 3: solution

C₁V₁ = C₂V₂
given: 9.00% (m/v) · 10.0 mL stock · water to 60.0 mL final · wanted: C₂ in % (m/v)
A common first attempt
C₂ = 9.00% × 10.0 mL50.0 mL water = 1.80% ✗
Step 1 · List the knowns Step 2 · Rearrange Step 3 · Match the units Step 4 · Substitute and solve
C₂ = 9.00% × 10.0 mL60.0 mL = 1.50% (m/v)
Dr. Karmach

Worked example 3: solution

C₁V₁ = C₂V₂
given: 9.00% (m/v) · 10.0 mL stock · water to 60.0 mL final · wanted: C₂ in % (m/v)
A common first attempt
C₂ = 9.00% × 10.0 mL50.0 mL water = 1.80% ✗
Step 1 · List the knowns Step 2 · Rearrange Step 3 · Match the units Step 4 · Substitute and solve
C₂ = 9.00% × 10.0 mL60.0 mL = 1.50% (m/v)
Grams check: 10.0 mL × 9.00 g/100 mL = 0.900 g NaOH, and 0.900 g in 60.0 mL is 1.50 g per 100 mL ✓
Dr. Karmach

Worked example 3: the route on the map

C₁V₁ = C₂V₂
given: 9.00% (m/v) · 10.0 mL stock · 60.0 mL final · found: C₂ = 1.50% (m/v)

The same path as worked example 1. Only the concentration unit changed: % with %. ✓
Dr. Karmach

Practice 3

C₁V₁ = C₂V₂
start 8.00% (m/v) KCl · 15.0 mL · plus 25.0 mL of water

A pharmacist mixes 15.0 mL of 8.00% (m/v) KCl with 25.0 mL of water. What is the new concentration, in % (m/v)?

  1. 3.00
  2. 4.80
  3. 21.3
  4. 1.20
Dr. Karmach

Practice 3 answer: A

C₁V₁ = C₂V₂
given: 8.00% (m/v) · 15.0 mL stock · 25.0 mL water added · wanted: C₂ in % (m/v)
V₂ = 15.0 mL + 25.0 mL = 40.0 mL → C₂ = 8.00% × 15.0 mL40.0 mL = 3.00% · answer A

B divided by the water alone, per solvent: 8.00 × (15.0 ÷ 25.0) = 4.80. C flipped the volume ratio: 8.00 × (40.0 ÷ 15.0) = 21.3, stronger than the start. D stopped at the solute: 15.0 mL × 8.00 g/100 mL = 1.20 g of KCl, not a percent.

The 1.20 g of KCl now sits in 40.0 mL of solution: 1.20 g ÷ 40.0 mL × 100 = 3.00% ✓
Dr. Karmach

Practice 3: the route on the map

C₁V₁ = C₂V₂
given: 8.00% (m/v) · 15.0 mL stock · 25.0 mL water added · found: C₂ = 3.00% (m/v)

The water was given, so V₂ = 15.0 + 25.0 = 40.0 mL first. Then C₂ = C₁ × V₁ ÷ V₂, the path of worked example 3. ✓
Dr. Karmach

Worked example 4: 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 4: 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 4: 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 4: 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 4: 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 4: 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 4: 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, as in the guided example. The new move is the unit: V₂ in liters, the answer wanted in mL. ✓
Dr. Karmach

Practice 4

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 4 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

Practice 4: the route on the map

M₁V₁ = M₂V₂
given: 0.400 M · 0.900 L final · stock 4.50 M · found: 820. mL of water added

V₂ entered in liters, so 0.900 L becomes 900. mL before the subtraction. Stock first, 80.0 mL, then water = 900. − 80.0. ✓
Dr. Karmach

Practice 5

C₁V₁ = C₂V₂
stock 18.0% (m/v) NaCl · target 0.900% (m/v) · final volume 3.00 L

A pharmacy prepares 3.00 L of 0.900% (m/v) saline from an 18.0% (m/v) NaCl stock. What volume of water, in mL, goes in with the measured stock?

  1. 150.
  2. 3.00 × 10³
  3. 2.85
  4. 27.0
  5. 2.85 × 10³
Dr. Karmach

Practice 5 answer: E

C₁V₁ = C₂V₂
given: 0.900% (m/v) · 3.00 L = 3.00 × 10³ mL final · 18.0% (m/v) stock · wanted: mL of water
V₁ = 3.00 × 10³ mL × 0.900%18.0% = 150. mL of stock
water = 3.00 × 10³ mL − 150. mL = 2.85 × 10³ mL · answer E

A stopped at the stock: 150. mL is what gets measured. B read 0.900% per solvent, 27.0 g NaCl per 3.00 × 10³ mL of water; the stock fills part of the 3.00 L. C subtracted in liters: 3.00 − 0.150 = 2.85 L, not mL. D stopped at the solute: 3.00 × 10³ mL × 0.900 g/100 mL = 27.0 g of NaCl.

The stock is 20 times stronger, so it fills a twentieth of the 3.00 L; water fills the rest ✓
Dr. Karmach

Practice 5: the route on the map

C₁V₁ = C₂V₂
given: 0.900% (m/v) · 3.00 L final · 18.0% (m/v) stock · found: 2.85 × 10³ mL of water

Concentrations pair % with %, volumes need L → mL: 3.00 L becomes 3.00 × 10³ mL, the stock is 150. mL, and water fills the rest. ✓
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

3 · 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; then explain, from the forces broken and formed, why dissolving can cool or warm the solution.

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

Structure decides what dissolves

like dissolves like
a solute dissolves in a solvent whose bonding and attractions are similar to its own
polar family: ionic compounds · molecules with O–H, N–H or a lopsided shape
table salt · water · ammonia
nonpolar family: molecules of only C and H · symmetric molecules
gasoline · vegetable oil · carbon dioxide

Sort baking soda (NaHCO₃) and propane (C₃H₈) into their families.

Dr. Karmach

Structure decides what dissolves

like dissolves like
a solute dissolves in a solvent whose bonding and attractions are similar to its own
polar family: ionic compounds · molecules with O–H, N–H or a lopsided shape
table salt · water · ammonia
nonpolar family: molecules of only C and H · symmetric molecules
gasoline · vegetable oil · carbon dioxide

Sort baking soda (NaHCO₃) and propane (C₃H₈) into their families.

baking soda: Na⁺ and HCO₃⁻ ions → polar family
propane: only C and H → nonpolar family
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

Dissolving a salt: forces broken, forces formed

the cost: ionic bonds in the solid break · hydrogen bonds between water molecules break
pulling the solute apart and the solvent apart both take energy
the payback: ion–dipole forces form between each ion and water
ion–dipole force = the attraction between an ion and a polar molecule · forming it releases energy

The heat of solution is the difference: energy to separate solute and solvent, less energy released as new attractions form. A molecular solute breaks its intermolecular forces instead of ionic bonds.

Dr. Karmach

Cold packs and hot packs

cost > payback → endothermic · the solution cools
the extra energy is drawn from the solution's own heat · KNO₃ or NH₄NO₃ in water: the cold pack
payback > cost → exothermic · the solution warms
the surplus energy is released as heat · CaCl₂ in water: the hot pack

Dissolving is favored by a drop in energy and by a rise in disorder as the solute spreads out. The disorder is why KNO₃ still dissolves despite the energy cost.

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

Guided example: carbon tetrachloride in hexane

a few drops of carbon tetrachloride (CCl₄) added to hexane (C₆H₁₄)
solute: CCl₄, four polar C–Cl bonds · solvent: hexane · wanted: dissolves or stays separate?

Carbon tetrachloride and hexane are both clear liquids. Do they dissolve in one another?

Sort each liquid into its family first, then match the families.

Dr. Karmach

Guided example: solution

solute: carbon tetrachloride (CCl₄) · solvent: hexane (C₆H₁₄)

Step 1 · Find the solute's polarity

ΔEN(C–Cl): 3.16 − 2.55 = 0.61 · polar bonds · symmetric tetrahedron → nonpolar solute

Each C–Cl bond is polar, but the four identical arrows point to the corners of a tetrahedron and cancel.

Dr. Karmach

Guided example: solution

solute: carbon tetrachloride (CCl₄) · solvent: hexane (C₆H₁₄)
Step 1 · Find the solute's polarity
ΔEN(C–Cl): 3.16 − 2.55 = 0.61 · polar bonds · symmetric tetrahedron → nonpolar solute
Step 2 · Find the solvent's polarity
C₆H₁₄: only C and H → nonpolar solvent

Hexane carries no charges and no polar groups.

Dr. Karmach

Guided example: solution

solute: carbon tetrachloride (CCl₄) · solvent: hexane (C₆H₁₄)
Step 1 · Find the solute's polarity
ΔEN(C–Cl): 3.16 − 2.55 = 0.61 · polar bonds · symmetric tetrahedron → nonpolar solute
Step 2 · Find the solvent's polarity
C₆H₁₄: only C and H → nonpolar solvent
Step 3 · Match them
nonpolar solute · nonpolar solvent → same family, they dissolve

Broken: CCl₄–CCl₄ and hexane–hexane dispersion. Formed: CCl₄–hexane dispersion.

Dr. Karmach

Guided example: solution

solute: carbon tetrachloride (CCl₄) · solvent: hexane (C₆H₁₄)
Step 1 · Find the solute's polarity
ΔEN(C–Cl): 3.16 − 2.55 = 0.61 · polar bonds · symmetric tetrahedron → nonpolar solute
Step 2 · Find the solvent's polarity
C₆H₁₄: only C and H → nonpolar solvent
Step 3 · Match them
nonpolar solute · nonpolar solvent → same family, they dissolve
CCl₄'s polar bonds cancel by shape. Old and new dispersion forces match, so they mix freely.
Dr. Karmach

Guided example: the route on the map

carbon tetrachloride (CCl₄) in hexane (C₆H₁₄)
nonpolar solute · nonpolar solvent · found: they dissolve in one another

Both liquids sit in the nonpolar family. Same family: they mix. ✓
Dr. Karmach

Practice 1: sodium iodide

sodium iodide, NaI
liquids on the shelf: hexane (C₆H₁₄) · carbon tetrachloride (CCl₄) · methanol (CH₃OH)

Which liquid dissolves sodium iodide?

  1. Hexane
  2. Methanol
  3. Carbon tetrachloride
  4. None of them: an ionic solid dissolves only in water
Dr. Karmach

Practice 1: answer B

sodium iodide, NaI: ionic · methanol, CH₃OH: polar, an O–H group
ionic solute · polar solvent · same family → it dissolves
NaI: Na⁺ and I⁻ ions → polar family · CH₃OH: an O–H group → polar solvent → it dissolves (answer B)

A paired an ionic solid with a nonpolar liquid, as if opposite polarities attract. C read CCl₄'s polar C–Cl bonds as a polar molecule; its symmetric shape cancels them. D treated water as the only polar solvent; methanol's O–H group makes it polar too.

Methanol's O–H end turns toward the ions, as water's does. Water is not the only polar solvent. ✓
Dr. Karmach

Practice 1: the route on the map

sodium iodide (NaI) in methanol (CH₃OH)
ionic solute · polar solvent · found: it dissolves

Ionic solute, polar solvent: one family. Any polar solvent, not only water, takes an ionic solute. ✓
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 2

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 2 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

Practice 2: the route on the map

naphthalene (C₁₀H₈) in hexane (C₆H₁₄)
nonpolar solute · nonpolar solvent · found: it dissolves

Only C and H in both: the nonpolar family on both sides, so naphthalene dissolves. ✓
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 3: two vitamins

vitamin A, C₂₀H₃₀O: one –OH group · vitamin C, C₆H₈O₆: four –OH groups
solvents: water · body fat

Which vitamin dissolves in water, and which in body fat?

  1. Vitamin C in water; vitamin A in body fat
  2. Both in water: each has at least one polar –OH group
  3. Vitamin A in water; vitamin C in body fat
  4. Both in body fat: both are built on carbon
Dr. Karmach

Practice 3: answer A

vitamin C, C₆H₈O₆: four –OH on six carbons → polar → water
vitamin A, C₂₀H₃₀O: one –OH on twenty carbons → nonpolar → body fat
vitamin C: 6 C ÷ 4 –OH = 1.5 C per –OH · vitamin A: 20 C ÷ 1 –OH = 20 C per –OH → answer A

B counted any –OH as enough; one –OH cannot carry a 20-carbon chain into water. C swapped the two families. D judged both by the carbon framework; vitamin C's four –OH groups make it polar.

Vitamin C has one –OH per 1.5 carbons, the same share as sugar, so it dissolves in water. Vitamin A's lone –OH is swamped by its carbon chain, so the body stores it in fat. ✓
Dr. Karmach

Practice 3: the route on the map

vitamin C (C₆H₈O₆) and vitamin A (C₂₀H₃₀O)
vitamin C: polar → water · vitamin A: nonpolar → body fat

Two routes, one rule: the share of –OH groups sets each vitamin's family. ✓
Dr. Karmach

Practice 4: a salt that cools the water

NH₄Cl(s) → NH₄⁺(aq) + Cl⁻(aq)
ammonium chloride dissolving in water · the solution turns cold

Which statement explains the cooling?

  1. Exothermic: breaking the ionic bonds in the solid releases energy
  2. Endothermic: forming ion–dipole forces with water absorbs energy
  3. Exothermic: the solution cools because dissolving releases heat
  4. Endothermic: forming ion–dipole forces releases more than separating costs
  5. Endothermic: separating ions and water costs more than ion–dipole forces release
Dr. Karmach

Practice 4: answer E

NH₄Cl(s) → NH₄⁺(aq) + Cl⁻(aq)
cost: ionic bonds and water's hydrogen bonds break · payback: ion–dipole forces form
cost > payback → endothermic: the solution cools (answer E)

A reversed bond breaking: pulling ions apart always costs energy. B reversed bond forming: forming ion–dipole forces releases energy. C read the cooling backwards: dissolving draws heat from the water, so the process absorbs it. D kept the label but flipped the comparison; a larger payback would warm the solution.

A solution that turns cold has paid more to separate than it got back. The heat came from the water itself. ✓
Dr. Karmach

Practice 5

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 5 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

Practice 5: the route on the map

CuSO₄ · erythritol (C₄H₁₀O₄) · β-carotene (C₄₀H₅₆) in water and hexane
ionic and polar solutes → water layer · nonpolar solute → hexane layer

Three solutes, three routes: each one follows its own family into the layer that matches. ✓
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?
  3. Lithium chloride dissolves in water and the solution turns warm. Is dissolving it endothermic or exothermic, and which is larger: the energy to separate the ions and the water molecules, or the energy released as ion–dipole forces form?

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

4 · 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, all of it dissolved)
Dr. Karmach

Three factors set the limit

structure · temperature · pressure (gases only)
like dissolves like · most solids dissolve more when hot, gases less · more gas pressure above the liquid, more gas dissolves

The solute and solvent, the temperature, and for a gas the pressure fix the limit. Warm water holds less dissolved oxygen, so fish in a warm pond can run short of it.

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 saturated plus solid. Cooling drops the excess out.
Dr. Karmach

The route through a saturation problem

Read the curve, scale it to the water, compare with the grams present. A cooled solution runs the lower lane too: the new limit sets what crystallizes.

Dr. Karmach

Guided example: more solid than the water holds

50. g KNO₃ stirred into 100. g of water at 30 °C
given: 50. g KNO₃ · 100. g water · curve at 30 °C: 46 g per 100 g water · wanted: grams left undissolved, and the type of solution

A student stirs until nothing more changes. A common first attempt: 50. g is more than the 46 g limit, so the solution is supersaturated.

Find the grams left on the bottom. Then classify the solution.

Dr. Karmach

Guided example: solution

50. g KNO₃ in 100. g of water at 30 °C
given: 50. g KNO₃ · 100. g water · curve at 30 °C: 46 g per 100 g water

Step 1 · Read the curve at the temperature

The KNO₃ curve at 30 °C reads 46 g per 100 g of water.

Dr. Karmach

Guided example: solution

50. g KNO₃ in 100. g of water at 30 °C
given: 50. g KNO₃ · 100. g water · curve at 30 °C: 46 g per 100 g water
Step 1 · Read the curve at the temperature Step 2 · Scale to the water present
100. g H₂O × 46 g KNO₃100 g H₂O = 46 g KNO₃ can dissolve

The beaker holds exactly 100 g of water, so the reading is the limit as it stands.

Dr. Karmach

Guided example: solution

50. g KNO₃ in 100. g of water at 30 °C
given: 50. g KNO₃ · 100. g water · curve at 30 °C: 46 g per 100 g water
Step 1 · Read the curve at the temperature Step 2 · Scale to the water present
100. g H₂O × 46 g KNO₃100 g H₂O = 46 g KNO₃ can dissolve
Step 3 · Compare with the limit
50. g added − 46 g limit = 4 g stay solid

46 g dissolves, then dissolving stops. The liquid holds the maximum, so it is saturated, not supersaturated.

Dr. Karmach

Guided example: solution

50. g KNO₃ in 100. g of water at 30 °C
given: 50. g KNO₃ · 100. g water · curve at 30 °C: 46 g per 100 g water
Step 1 · Read the curve at the temperature Step 2 · Scale to the water present
100. g H₂O × 46 g KNO₃100 g H₂O = 46 g KNO₃ can dissolve
Step 3 · Compare with the limit
50. g added − 46 g limit = 4 g stay solid
Solid resting in the liquid marks a saturated solution. A supersaturated one holds the extra dissolved, with no solid present. ✓
Dr. Karmach

Guided example: the route on the map

50. g KNO₃ in 100. g of water at 30 °C
given: 50. g KNO₃ · 100. g water · found: 46 g dissolve · 4 g stay solid · saturated

Top lane: read, scale, compare. Above the limit, the extra stays solid and the solution is saturated. ✓
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

Practice 1: the limit for this water

KCl at 20 °C: 34.0 g per 100 mL of water
a beaker holds 450. mL of water at 20 °C

What is the most KCl, in grams, that this water can dissolve?

  1. 153
  2. 7.56
  3. 34.0
  4. 1.32 × 10³
Dr. Karmach

Practice 1 answer: A

KCl at 20 °C: 34.0 g per 100 mL water · 450. mL of water
the reading is per 100 mL, so scale it by the mL of water
450. mL H₂O × 34.0 g KCl100 mL H₂O = 153 g KCl · answer A

B scaled the wrong way: 34.0 × (100/450.) = 7.56. C used 34.0 g unscaled, the limit for 100 mL of water. D flipped the solubility: 450. × (100/34.0) = 1.32 × 10³, and mL H₂O does not cancel.

450. mL is 4.50 times 100 mL, so the limit is 4.50 × 34.0 = 153 g. ✓
Dr. Karmach

Practice 1: the route on the map

KCl at 20 °C: 34.0 g per 100 mL water
given: 450. mL of water · found: 153 g KCl can dissolve

Steps 1 and 2 only, scaled by mL of water. With no KCl added, there is nothing to compare. ✓
Dr. Karmach

Practice 2: room left in the beaker

75.0 g of KI already dissolved in 125 g of water at 20 °C
KI at 20 °C: 144 g per 100 g of water

How many more grams of KI will this beaker take up?

  1. 180.
  2. 105
  3. 255
  4. 69.0
Dr. Karmach

Practice 2 answer: B

KI at 20 °C: 144 g per 100 g water · 75.0 g dissolved in 125 g of water
scale the limit to 125 g of water, then compare
125 g H₂O × 144 g KI100 g H₂O = 180. g limit
180. g limit − 75.0 g present = 105 g more · answer B

A stopped at the limit: 180. g counts the 75.0 g already in. C added instead of subtracting: 180. + 75.0 = 255. D used 144 g unscaled: 144 − 75.0 = 69.0.

75.0 g + 105 g = 180. g, the full limit for 125 g of water. ✓
Dr. Karmach

Practice 2: the route on the map

KI at 20 °C: 144 g per 100 g water
given: 75.0 g KI · 125 g water · found: limit 180. g · 105 g more · unsaturated

The whole top lane: read, scale, compare. The grams present sit below the limit. ✓
Dr. Karmach

Practice 3: three beakers of Ca(OH)₂

Ca(OH)₂ at 30 °C: 0.15 g per 100 g of water
beaker 1: 0.30 g in 200. g water · beaker 2: 0.50 g in 500. g water · beaker 3: 0.40 g in 120. g water

Each beaker is stirred at 30 °C until nothing more changes. Classify beakers 1, 2 and 3, in that order.

  1. saturated · unsaturated · supersaturated
  2. saturated · saturated · saturated
  3. saturated · unsaturated · saturated
  4. unsaturated · unsaturated · saturated
Dr. Karmach

Practice 3 answer: C

Ca(OH)₂ at 30 °C: 0.15 g per 100 g water
each limit = g of water × 0.15 g / 100 g water, then compare with the grams added
beaker water limit added solution
1 200. g 0.30 g 0.30 g saturated
2 500. g 0.75 g 0.50 g unsaturated
3 120. g 0.18 g 0.40 g saturated + solid
beaker 3: 0.40 g added − 0.18 g limit = 0.22 g stays solid · answer C

A called beaker 3 supersaturated, but its extra stays solid. B compared every beaker with 0.15 g unscaled. D called beaker 1 unsaturated, yet 0.30 g is its full limit.

Beaker 2 holds the most Ca(OH)₂ yet has 0.25 g of room. The water sets the limit. ✓
Dr. Karmach

Practice 3: the route on the map

beaker 1: 0.30 g Ca(OH)₂ in 200. g water at 30 °C
found: limit 0.30 g · 0.30 g added · saturated, no solid left

Added equals the limit: saturated. Beakers 2 and 3 take the below and above boxes. ✓
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 4

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 4 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 4: the route on the map

NaCl at 20 °C: 36 g per 100 g water · 75 g into 50. g water
found: 18 g dissolve · 57 g stay solid

Scaling halves the 36 g reading. 75 g is far above the 18 g limit, so the excess stays on the bottom. ✓
Dr. Karmach

Practice 5: cooling a saturated solution

K₂Cr₂O₇: 73.0 g per 100 g water at 80 °C · 12.0 g per 100 g water at 20 °C
a solution saturated with K₂Cr₂O₇ in 40.0 g of water at 80 °C is cooled to 20 °C

How many grams of K₂Cr₂O₇ crystallize?

  1. 24.4
  2. 4.80
  3. 61.0
  4. 17.2
Dr. Karmach

Practice 5 answer: A

saturated K₂Cr₂O₇ in 40.0 g water · 80 °C → 20 °C
scale both limits to 40.0 g of water
40.0 g H₂O × 73.0 g K₂Cr₂O₇100 g H₂O = 29.2 g dissolved at 80 °C
40.0 g H₂O × 12.0 g K₂Cr₂O₇100 g H₂O = 4.80 g stays · 29.2 − 4.80 = 24.4 g crystallize · answer A

B stopped at 4.80 g, what stays dissolved. C used both readings unscaled: 73.0 − 12.0 = 61.0. D scaled the 80 °C reading but not the 20 °C one: 29.2 − 12.0 = 17.2.

40.0 g of water is 0.400 of 100 g, so 0.400 × 61.0 = 24.4 g crystallize. ✓
Dr. Karmach

Practice 5: the route on the map

saturated K₂Cr₂O₇ in 40.0 g water · 80 °C → 20 °C
found: 29.2 g dissolved · new limit 4.80 g · 24.4 g crystallize

Saturated start: the 80 °C limit is the grams dissolved. Both lanes scale by 40.0 g / 100 g. ✓
Dr. Karmach

Practice 6

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 6 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

Practice 6: the route on the map

180. g KNO₃ in 250. g water · 70 °C → 30 °C
found: 340. g limit at 70 °C · 115 g limit at 30 °C · 65 g crystallize

Both lanes: all 180. g dissolve at 70 °C, and the excess over 115 g crystallizes. ✓
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

5 · 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

Pressure changes gas solubility only

three factors set solubility: structure · temperature · pressure
pressure matters for a gas solute only · a dissolved solid or liquid does not respond

Pressure pushes a gas into a liquid. A dissolved solid does not respond.

Sugar water and soda water are sealed under more pressure. Which solubility rises?

Dr. Karmach

Pressure changes gas solubility only

three factors set solubility: structure · temperature · pressure
pressure matters for a gas solute only · a dissolved solid or liquid does not respond

Pressure pushes a gas into a liquid. A dissolved solid does not respond.

Sugar water and soda water are sealed under more pressure. Which solubility rises?

The CO₂. Sugar is a solid. ✓
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

Henry's law in symbols

C₁/P₁ = C₂/P₂, also written S₁/P₁ = S₂/P₂
C or S: the gas's solubility, a concentration · P: its partial pressure · same gas, constant temperature

Any concentration unit works for S: g/L, mg/L, g/100 mL or M. Any pressure unit works for P: atm or mmHg. Keep each pair in one unit so it cancels.

S₂ = S₁ in mg/L × P₂ in mmHgP₁ in mmHg = S₂ in mg/L
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

Guided example: a mountain lake

S₁/P₁ = S₂/P₂
given: S₁ = 9.0 mg/L · P₁ = 160 mmHg · P₂ = 80. mmHg · same gas, constant temperature · wanted: S₂

A lake at sea level holds 9.0 mg/L of dissolved O₂ under 160 mmHg of O₂. A high mountain lake at the same temperature sits under only 80. mmHg of O₂. How much O₂ can it hold, in mg/L?

Compare the pressures first: 80. mmHg is half of 160 mmHg.

Dr. Karmach

Guided example: solution

S₁/P₁ = S₂/P₂
given: S₁ = 9.0 mg/L · P₁ = 160 mmHg · P₂ = 80. mmHg · wanted: S₂

The O₂ pressure halves, so the dissolved O₂ should halve too: about 4.5 mg/L. The four method steps give the exact value.

Dr. Karmach

Guided example: solution

S₁/P₁ = S₂/P₂
given: S₁ = 9.0 mg/L · P₁ = 160 mmHg · P₂ = 80. mmHg · wanted: S₂
Step 1 · Identify given and wanted

Given: S₁ = 9.0 mg/L at P₁ = 160 mmHg, and P₂ = 80. mmHg. Same gas, same temperature. Wanted: S₂, the new solubility.

Dr. Karmach

Guided example: solution

S₁/P₁ = S₂/P₂
given: S₁ = 9.0 mg/L · P₁ = 160 mmHg · P₂ = 80. mmHg · wanted: S₂
Step 1 · Identify given and wanted Step 2 · Set up the proportion

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

Dr. Karmach

Guided example: solution

S₁/P₁ = S₂/P₂
given: S₁ = 9.0 mg/L · P₁ = 160 mmHg · P₂ = 80. mmHg · 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

Multiply both sides by P₂. The new pressure lands on top.

Dr. Karmach

Guided example: solution

S₁/P₁ = S₂/P₂
given: S₁ = 9.0 mg/L · P₁ = 160 mmHg · P₂ = 80. mmHg · 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 = 9.0 mg/L × 80. mmHg160 mmHg = 4.5 mg/L
The O₂ pressure halved, so half as much O₂ dissolves: 9.0 → 4.5 mg/L. mmHg cancels and mg/L carries through. ✓
Dr. Karmach

Guided example: the route on the strip

S₁/P₁ = S₂/P₂
given: 9.0 mg/L at 160 mmHg · P₂ = 80. mmHg · found: S₂ = 4.5 mg/L

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

Practice 1

S₁/P₁ = S₂/P₂
given: S₁ = 42.0 mg/L · P₁ = 2.40 atm · P₂ = 0.800 atm · same gas, constant temperature · wanted: S₂

At depth, a diver's blood holds 42.0 mg/L of N₂ under 2.40 atm of N₂. At the surface the N₂ pressure is 0.800 atm. How many milligrams of N₂ per liter can her blood hold there?

  1. 126
  2. 28.0
  3. 42.0
  4. 14.0
Dr. Karmach

Practice 1 answer: D

S₁/P₁ = S₂/P₂
N₂ · S₁ = 42.0 mg/L at P₁ = 2.40 atm · P₂ = 0.800 atm · constant temperature
S₂ = 42.0 mg/L × 0.800 atm2.40 atm = 14.0 mg/L · answer D

A inverted the proportion like Boyle's law: 42.0 × (2.40/0.800) = 126 mg/L, more N₂ held at lower pressure. B scaled by the pressure change: 42.0 × (2.40 − 0.800)/2.40 = 28.0 mg/L, the N₂ that comes out, not what stays. C assumed no change: at a third of the pressure, 42.0 mg/L cannot stay dissolved.

The pressure fell to a third, so a third of the N₂ stays dissolved: 42.0 → 14.0 mg/L. The other 28.0 mg/L leaves the blood. ✓
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 again. 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 2

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 2 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 3

S₁/P₁ = S₂/P₂
given: S₁ = 0.140 M at P₁ = 4.20 atm · S₂ = 0.0850 M · same gas, constant temperature · wanted: P₂

A soda fountain's carbonator holds water at 0.140 M CO₂ under 4.20 atm of CO₂. What CO₂ pressure, in atm, gives 0.0850 M at the same temperature?

  1. 2.55
  2. 6.92
  3. 0.607
  4. 4.20
Dr. Karmach

Practice 3 answer: A

S₁/P₁ = S₂/P₂
CO₂ · S₁ = 0.140 M at P₁ = 4.20 atm · target S₂ = 0.0850 M · wanted: P₂
P₂ = 4.20 atm × 0.0850 M0.140 M = 2.55 atm · answer A

B inverted the ratio like Boyle's law: 4.20 × (0.140/0.0850) = 6.92 atm, more pressure for less dissolved gas. C stopped at the ratio: 0.0850/0.140 = 0.607, never multiplied by P₁. D assumed no change: a lower concentration needs a lower pressure.

The concentration falls to 0.607 of its value, so the pressure falls to 0.607 × 4.20 atm = 2.55 atm. ✓
Dr. Karmach

Practice 4

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 4 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 4 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

Practice 4: the route on the strip

S₁/P₁ = S₂/P₂
given: CH₄ 0.0460 g/L at 2.00 atm · 6.00 atm → 1.50 atm · 0.400 L · found: 0.0414 g released

Two trips through the top lane give each solubility: 0.138 g/L at 6.00 atm and 0.0345 g/L at 1.50 atm. The bottom lane turns the 0.1035 g/L drop into grams: × 0.400 L = 0.0414 g. ✓
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 gives a gas's concentration in g/L, mg/L or M. Percent concentration describes any solution's makeup a different way: grams of solute per 100 g of solution.

Dr. Karmach

6 · Percent Concentration

Compute a solution's mass, volume, or mass-volume percent, and use a labeled percent as a conversion factor between the amount of solution and the amount of solute.

Dr. Karmach

Three labels, three percents

Peroxide reads 3%. Saline reads 0.9%. Rubbing alcohol reads 70%. On every label, the number compares the active ingredient to everything in the bottle.

Dr. Karmach

Concentration: solute compared to solution

concentration = amount of solute ÷ amount of solution
solute: the substance dissolved · solvent: what it dissolves in, usually water · solution = solute + solvent

More solute alone does not mean more concentrated.

Which drink is more concentrated: 10.0 g of sugar in 200. g of drink, or 15.0 g in 500. g?

Dr. Karmach

Concentration: solute compared to solution

concentration = amount of solute ÷ amount of solution
solute: the substance dissolved · solvent: what it dissolves in, usually water · solution = solute + solvent

More solute alone does not mean more concentrated.

Which drink is more concentrated: 10.0 g of sugar in 200. g of drink, or 15.0 g in 500. g?

10.0 g sugar200. g drink = 5.00 g per 100 g ✓    15.0 g sugar500. g drink = 3.00 g per 100 g

The first drink, with less sugar.

Dr. Karmach

Percent concentration: parts per hundred

Seawater carries 3.5 g of dissolved salts in every 100 g. A percent concentration states the parts of solute in every hundred parts of solution. The hundred is the whole solution: solute plus solvent.

Dr. Karmach

Mass, volume, and mass-volume percent

Each type is the same fraction, part over whole solution, in its own units. Molarity counts moles per liter; a percent needs no molar mass, only a balance or a graduated cylinder.

Dr. Karmach

A percent label is an equality

3.0% (m/m) hydrogen peroxide: 3.0 g H₂O₂ = 100 g solution
every 100 g of solution carries 3.0 g of H₂O₂; the other 97.0 g is water

Every equality gives a conversion factor. This one links solute mass to solution mass:

3.0 g H₂O₂100 g solution or 100 g solution3.0 g H₂O₂

Write it so the given unit cancels.

Dr. Karmach

The method

  1. Name part and whole: the whole solution, solute plus solvent.
  2. Match the units: m/m g/g, v/v mL/mL, m/v g/mL.
  3. Write the fraction: part over whole × 100, or the orientation that cancels the given.
  4. Multiply and check.
Dr. Karmach

One map for every percent problem

To find a percent, divide part by whole, × 100. To use a label, its factor carries solution to solute, or back. Liters, a density, or a separate solvent reach the whole first.

Dr. Karmach

Guided example: sugar in a sports drink

Step 1 · Name part and whole

18.0 g sugar · final volume 0.300 L
part: sugar · whole: 0.300 L of drink, sugar included · wanted: m/v %

A bottle of sports drink carries 18.0 g of sugar in a final volume of 0.300 L. What is its mass-volume percent of sugar?

A final volume is already the whole solution. Nothing gets added to it.

Dr. Karmach

Guided example: solution

18.0 g sugar · final volume 0.300 L
part: sugar · whole: 0.300 L of drink · wanted: m/v %

Step 2 · Match the units

m/v pairs grams of solute with milliliters of solution. The whole converts to milliliters:

0.300 L × 1000 mL1 L = 300. mL solution
Dr. Karmach

Guided example: solution

18.0 g sugar · final volume 0.300 L
part: sugar · whole: 0.300 L of drink · wanted: m/v %
Step 2 · Match the units
0.300 L × 1000 mL1 L = 300. mL solution
Step 3 · Write the fraction

Part over whole, × 100, with the whole in milliliters. Left in liters, the fraction runs far above 100:

18.0 g sugar300. mL solution g over mL ✓    18.0 g sugar0.300 L solution × 100 = 6.00 × 10³ ✗
Dr. Karmach

Guided example: solution

18.0 g sugar · final volume 0.300 L
part: sugar · whole: 0.300 L of drink · wanted: m/v %
Step 2 · Match the units
0.300 L × 1000 mL1 L = 300. mL solution
Step 3 · Write the fraction Step 4 · Multiply and check
18.0 g sugar300. mL solution × 100 = 6.00% (m/v)
Dr. Karmach

Guided example: solution

18.0 g sugar · final volume 0.300 L
part: sugar · whole: 0.300 L of drink · wanted: m/v %
Step 2 · Match the units
0.300 L × 1000 mL1 L = 300. mL solution
Step 3 · Write the fraction Step 4 · Multiply and check
18.0 g sugar300. mL solution × 100 = 6.00% (m/v)
6.00 g of sugar in every 100 mL, and the bottle holds three hundreds: 18.0 g. ✓
Dr. Karmach

Guided example: the route on the map

18.0 g sugar · final volume 0.300 L
given: 18.0 g sugar · 0.300 L of drink · found: 6.00% (m/v)

Two moves: liters to milliliters for the whole, then part over whole × 100. ✓
Dr. Karmach

Practice 1

hand sanitizer: 260. mL ethanol in a 400. mL bottle
given: 260. mL solute · 400. mL solution · wanted: v/v %

A 400. mL bottle of hand sanitizer holds 260. mL of ethanol. What is the volume percent of ethanol?

  1. 186
  2. 0.650
  3. 65.0
  4. 154
  5. 39.4
Dr. Karmach

Practice 1: answer C

260. mL ethanol in a 400. mL bottle
part: ethanol · whole: 400. mL solution, ethanol included · wanted: v/v %
260. mL ethanol400. mL solution × 100 = 65.0% (v/v), answer C

A compared the ethanol to the other 140. mL alone: 260. / 140. × 100 = 186. B stopped at the decimal fraction: 260. / 400. = 0.650. D flipped part and whole: 400. / 260. × 100 = 154. E added the ethanol to a volume that already held it: 260. / 660. × 100 = 39.4.

The bottle's 400. mL is the whole, ethanol included. Every 100 mL of sanitizer carries 65.0 mL of ethanol. ✓
Dr. Karmach

Worked example 1: mass percent from masses

25.0 g sucrose dissolved in 100.0 g water
given: 25.0 g solute · 100.0 g solvent · wanted: m/m %

A café batch of simple syrup: 25.0 g of sucrose dissolved in 100.0 g of water. What is the mass percent of sucrose?

A common first attempt: divide the 25.0 g of sucrose by the 100.0 g of water. Test the denominator.

Dr. Karmach

Worked example 1: solution

given: 25.0 g sucrose + 100.0 g water · wanted: m/m %

A common first attempt

25.0 g sucrose100.0 g water × 100 = 25.0% ✗

That ratio compares the sucrose to the water alone. A mass percent compares it to the whole solution.

Dr. Karmach

Worked example 1: solution

given: 25.0 g sucrose + 100.0 g water · wanted: m/m %
A common first attempt
25.0 g sucrose100.0 g water × 100 = 25.0% ✗
Step 1 · Name part and whole

The whole is everything in the beaker, solute plus solvent: 25.0 g + 100.0 g = 125.0 g of solution.

Dr. Karmach

Worked example 1: solution

given: 25.0 g sucrose + 100.0 g water · wanted: m/m %
A common first attempt
25.0 g sucrose100.0 g water × 100 = 25.0% ✗
Step 1 · Name part and whole Step 2 · Match the units Step 3 · Write the fraction

Both measurements are masses: m/m, grams over grams. Part over whole, × 100.

Dr. Karmach

Worked example 1: solution

given: 25.0 g sucrose + 100.0 g water · wanted: m/m %
A common first attempt
25.0 g sucrose100.0 g water × 100 = 25.0% ✗
Step 1 · Name part and whole Step 2 · Match the units Step 3 · Write the fraction Step 4 · Multiply and check
25.0 g sucrose125.0 g solution × 100 = 20.0% (m/m)
Dr. Karmach

Worked example 1: solution

given: 25.0 g sucrose + 100.0 g water · wanted: m/m %
A common first attempt
25.0 g sucrose100.0 g water × 100 = 25.0% ✗
Step 1 · Name part and whole Step 2 · Match the units Step 3 · Write the fraction Step 4 · Multiply and check
25.0 g sucrose125.0 g solution × 100 = 20.0% (m/m)
One fifth of 125.0 g is sugar: 20.0 g per 100 g syrup; water alone gives 25.0%, too high. ✓
Dr. Karmach

Worked example 1: the route on the map

25.0 g sucrose dissolved in 100.0 g water
given: 25.0 g solute · 100.0 g solvent · found: 125.0 g solution · 20.0% (m/m)

Two moves: the solute joins the solvent to make the whole, then part over whole × 100. ✓
Dr. Karmach

Worked example 2: solute mass from the label

Step 1 · Name part and whole

3.0% (m/m) hydrogen peroxide: 3.0 g H₂O₂ = 100 g solution
part: H₂O₂ · whole: solution · given: 250.0 g solution · wanted: g H₂O₂

A drugstore bottle holds 250.0 g of 3.0% (m/m) hydrogen peroxide solution. What mass of H₂O₂ is in the bottle?

Set it up: which orientation of the percent factor cancels g solution?

Dr. Karmach

Worked example 2: solution

3.0% (m/m) hydrogen peroxide: 3.0 g H₂O₂ = 100 g solution
part: H₂O₂ · whole: solution · given: 250.0 g solution · wanted: g H₂O₂

One conversion factor is needed.

Step 2 · Match the units

m/m pairs grams of solute with grams of solution, so the label declares 3.0 g H₂O₂ = 100 g solution.

Dr. Karmach

Worked example 2: solution

3.0% (m/m) hydrogen peroxide: 3.0 g H₂O₂ = 100 g solution
part: H₂O₂ · whole: solution · given: 250.0 g solution · wanted: g H₂O₂
Step 2 · Match the units Step 3 · Write the fraction

The equality gives two orientations. Only one cancels the given unit, g solution:

3.0 g H₂O₂100 g solution cancels g solution ✓    100 g solution3.0 g H₂O₂ cancels nothing ✗
Dr. Karmach

Worked example 2: solution

3.0% (m/m) hydrogen peroxide: 3.0 g H₂O₂ = 100 g solution
part: H₂O₂ · whole: solution · given: 250.0 g solution · wanted: g H₂O₂
Step 2 · Match the units Step 3 · Write the fraction Step 4 · Multiply and check
250.0 g solution × 3.0 g H₂O₂100 g solution = 7.5 g H₂O₂
Dr. Karmach

Worked example 2: solution

3.0% (m/m) hydrogen peroxide: 3.0 g H₂O₂ = 100 g solution
part: H₂O₂ · whole: solution · given: 250.0 g solution · wanted: g H₂O₂
Step 2 · Match the units Step 3 · Write the fraction Step 4 · Multiply and check
250.0 g solution × 3.0 g H₂O₂100 g solution = 7.5 g H₂O₂
The label promises 3.0 g in every 100 g, and 250.0 g is two and a half hundreds: 7.5 g of H₂O₂. The other 242.5 g is water. ✓
Dr. Karmach

Worked example 2: the route on the map

3.0% (m/m) hydrogen peroxide: 3.0 g H₂O₂ = 100 g solution
given: 250.0 g solution · found: 7.5 g H₂O₂

The given is already the label's whole, grams of solution. One move: the label factor carries it to the solute. ✓
Dr. Karmach

Your turn: rubbing alcohol

70.0% (v/v) isopropyl alcohol: 70.0 mL alcohol = 100 mL solution
given: 350.0 mL solution · wanted: mL alcohol

A full 350.0 mL bottle of rubbing alcohol is 70.0% (v/v) isopropyl alcohol.

350.0 mL solution × mL alcohol mL solution = mL alcohol

Fill the factor from the label so mL solution cancels, then compute.

Dr. Karmach

Your turn: rubbing alcohol

70.0% (v/v) isopropyl alcohol: 70.0 mL alcohol = 100 mL solution
given: 350.0 mL solution · wanted: mL alcohol

A full 350.0 mL bottle of rubbing alcohol is 70.0% (v/v) isopropyl alcohol.

350.0 mL solution × mL alcohol mL solution = mL alcohol

Fill the factor from the label so mL solution cancels, then compute.

350.0 mL solution × 70.0 mL alcohol100 mL solution = 245 mL alcohol
Dr. Karmach

Where this goes wrong

Dividing by the solvent alone. 25.0 g of sucrose in 100.0 g of water: 25.0 / 100.0 × 100 = 25.0%. The sucrose is part of the whole, so the denominator is 25.0 + 100.0 = 125.0 g of solution: 20.0%.
Flipping part and whole. 125.0 / 25.0 × 100 = 500., above 100. A percent concentration never tops 100, because the part never outweighs its whole. Part over whole gives 20.0%.
Dropping the × 100. 25.0 / 125.0 = 0.200, the decimal fraction, not a percent. Per hundred: 20.0%.
Using the raw percent in a chain. For 250.0 g of a 3.0% (m/m) solution, 250.0 × 3.0 = 750, one hundred times too much. The label means 3.0 g per 100 g of solution; the factor 3.0 g / 100 g gives 7.5 g.
Dr. Karmach

Practice 2

20.0 g KBr dissolved in 230.0 g water
given: 20.0 g solute · 230.0 g solvent · wanted: m/m %

A stockroom solution is prepared by dissolving 20.0 g of potassium bromide (KBr) in 230.0 g of water. What is the mass percent of KBr?

  1. 8.00
  2. 8.70
  3. 1.25 × 10³
  4. 0.0800
Dr. Karmach

Practice 2: answer A

20.0 g KBr + 230.0 g water = 250.0 g solution
given: 20.0 g solute · 230.0 g solvent · wanted: m/m %
20.0 g KBr250.0 g solution × 100 = 8.00% (m/m), answer A

B divided by the water alone: 20.0 / 230.0 × 100 = 8.70. C flipped part and whole: 250.0 / 20.0 × 100 = 1.25 × 10³, and no percent concentration tops 100. D stopped at the decimal fraction: 20.0 / 250.0 = 0.0800; the × 100 makes it 8.00 per hundred.

Every 100 g of solution carries 8.00 g of KBr, and the whole 250.0 g carries two and a half times that: 20.0 g. ✓
Dr. Karmach

Worked example 3: solution volume from a solute mass

Step 1 · Name part and whole

0.90% (m/v) saline: 0.90 g NaCl = 100 mL solution
part: NaCl · whole: solution · given: 4.5 g NaCl · wanted: mL solution

Normal saline is 0.90% (m/v): grams of NaCl per 100 milliliters of solution. An IV order calls for 4.5 g of NaCl. What volume of saline delivers it?

Set it up so g NaCl cancels.

Dr. Karmach

Worked example 3: solution

0.90% (m/v) saline: 0.90 g NaCl = 100 mL solution
part: NaCl · whole: solution · given: 4.5 g NaCl · wanted: mL solution

One conversion factor is needed.

Step 2 · Match the units

m/v pairs grams of solute with milliliters of solution: the one percent that crosses between mass and volume, the way a density does.

Dr. Karmach

Worked example 3: solution

0.90% (m/v) saline: 0.90 g NaCl = 100 mL solution
part: NaCl · whole: solution · given: 4.5 g NaCl · wanted: mL solution
Step 2 · Match the units Step 3 · Write the fraction

The given is a mass of NaCl, so g NaCl belongs in the denominator: 100 mL solution over 0.90 g NaCl.

Dr. Karmach

Worked example 3: solution

0.90% (m/v) saline: 0.90 g NaCl = 100 mL solution
part: NaCl · whole: solution · given: 4.5 g NaCl · wanted: mL solution
Step 2 · Match the units Step 3 · Write the fraction Step 4 · Multiply and check
4.5 g NaCl × 100 mL solution0.90 g NaCl = 5.0 × 10² mL solution
Dr. Karmach

Worked example 3: solution

0.90% (m/v) saline: 0.90 g NaCl = 100 mL solution
part: NaCl · whole: solution · given: 4.5 g NaCl · wanted: mL solution
Step 2 · Match the units Step 3 · Write the fraction Step 4 · Multiply and check
4.5 g NaCl × 100 mL solution0.90 g NaCl = 5.0 × 10² mL solution
Every 100 mL of saline carries 0.90 g of NaCl, and 4.5 g is five of those hundreds: 5.0 × 10² mL, one standard IV bag. ✓
Dr. Karmach

Worked example 3: the route on the map

0.90% (m/v) saline: 0.90 g NaCl = 100 mL solution
given: 4.5 g NaCl · found: 5.0 × 10² mL solution

The given is the part, so the label factor runs flipped: solute to solution. One move. ✓
Dr. Karmach

Practice 3

IV bag: 15.0% (m/v) mannitol
given: 0.500 L solution · wanted: g mannitol

An IV bag holds 0.500 L of 15.0% (m/v) mannitol solution. How many grams of mannitol does it deliver?

  1. 65.2
  2. 0.0750
  3. 3.33 × 10³
  4. 75.0
  5. 7.50 × 10³
Dr. Karmach

Practice 3: answer D

15.0% (m/v): 15.0 g mannitol = 100 mL solution
given: 0.500 L solution · wanted: g mannitol · the label's whole is mL

Two conversion factors are needed.

0.500 L soln × 1000 mL soln1 L soln × 15.0 g mannitol100 mL soln = 75.0 g mannitol (answer D)

A read the label as 15.0 g per 100 mL of water, as if 115 parts made the solution: 500. × 15.0 / 115 = 65.2. B skipped liters to milliliters: 0.500 × 15.0 / 100 = 0.0750. C flipped the label factor: 500. × 100 / 15.0 = 3.33 × 10³. E used the raw percent: 500. × 15.0 = 7.50 × 10³.

15.0 g in every 100 mL, and 500. mL is five hundreds: 75.0 g. ✓
Dr. Karmach

Practice 3: the route on the map

15.0% (m/v): 15.0 g mannitol = 100 mL solution
given: 0.500 L solution · found: 75.0 g mannitol

The label's whole is milliliters, so liters convert first. Then the label factor carries solution to solute. ✓
Dr. Karmach

Practice 4

concentrated aqueous ammonia: 28.0% (m/m) NH₃ · density 0.900 g/mL
given: 250. mL solution · wanted: g NH₃

A stockroom bottle holds 250. mL of concentrated aqueous ammonia, 28.0% (m/m) NH₃, with a density of 0.900 g/mL. How many grams of NH₃ does it hold?

  1. 70.0
  2. 63.0
  3. 225
  4. 77.8
Dr. Karmach

Practice 4: answer B

28.0% (m/m): 28.0 g NH₃ = 100 g solution · 0.900 g solution = 1 mL solution
m/m pairs grams with grams: the density turns mL of solution into g first
250. mL soln × 0.900 g soln1 mL soln × 28.0 g NH₃100 g soln = 63.0 g NH₃ (answer B)

A skipped the density: 250. × 28.0 / 100 = 70.0 treats mL of solution as grams. C stopped halfway: 250. × 0.900 = 225 g is the whole solution, not the NH₃ in it. D flipped the density: 250. ÷ 0.900 = 278 g, then × 28.0 / 100 = 77.8.

The liquid is lighter than water, so 250. mL weighs less than 250 g, and the NH₃ lands below the 70.0 g a density of 1 would give: 63.0 g. ✓
Dr. Karmach

Practice 4: the route on the map

28.0% (m/m) NH₃ · density 0.900 g/mL
given: 250. mL solution · found: 63.0 g NH₃

An m/m label counts grams of solution, so the density turns milliliters into grams first. Then the label factor. ✓
Dr. Karmach

7 · Molality & Mole Fraction

Calculate the molality of a solution from grams of solute and grams of solvent and explain why it does 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

Three concentration units, three denominators

mass percent = g solute ÷ g solution × 100
molarity, M = mol solute ÷ L solution
molality, m = mol solute ÷ kg solvent
solution = solute + solvent · the solute always sits on top

Every concentration puts the solute on top. The denominators differ: the solution's mass, the solution's volume, or the solvent's mass.

Which denominator leaves the solute out?

Dr. Karmach

Three concentration units, three denominators

mass percent = g solute ÷ g solution × 100
molarity, M = mol solute ÷ L solution
molality, m = mol solute ÷ kg solvent
solution = solute + solvent · the solute always sits on top

Every concentration puts the solute on top. The denominators differ: the solution's mass, the solution's volume, or the solvent's mass.

Which denominator leaves the solute out?
Molality's: the solvent alone, in kilograms.

Dr. Karmach

Measured by amount and mass, not volume

Molarity divides by the solution's volume, and volume swells when warmed. Molality counts moles and weighs mass, so temperature does not change it.

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

A molality is an equality

1.50 m glucose: 1.50 mol glucose = 1 kg water
every kilogram of water carries 1.50 mol of glucose

Every equality gives a conversion factor. This one links moles of solute to kilograms of solvent:

1.50 mol glucose1 kg water or 1 kg water1.50 mol glucose

Write it so the given unit cancels.

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 does not.

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

One map for every molality problem

Forward: solute grams become moles, solvent grams become kilograms, then moles ÷ kilograms. Backward: the molality, either way up, crosses between the two. A total solution mass loses its solute first.

Dr. Karmach

Guided example: brine for an ice-cream maker

Step 1 · Grams → moles

m = mol solute ÷ kg solvent
given: 1.20 mol NaCl · 800. g water · wanted: m

An old-fashioned ice-cream maker packs its tub in a brine of 1.20 mol of NaCl dissolved in 800. g of water. Find the molality.

The salt is already counted in moles, so no molar mass is needed.

Dr. Karmach

Guided example: solution

m = mol solute ÷ kg solvent
given: 1.20 mol NaCl · 800. g water · wanted: m

Per kilogram: 800. g is less than a kilogram of water, so a full kilogram would carry more than 1.20 mol.

Dr. Karmach

Guided example: solution

m = mol solute ÷ kg solvent
given: 1.20 mol NaCl · 800. g water · wanted: m
Step 2 · Grams → kilograms
800. g water = 0.800 kg water
1000 g = 1 kg · molality counts kilograms of the solvent
Dr. Karmach

Guided example: solution

m = mol solute ÷ kg solvent
given: 1.20 mol NaCl · 800. g water · wanted: m
Step 2 · Grams → kilograms
800. g water = 0.800 kg water
1000 g = 1 kg · molality counts kilograms of the solvent
Step 3 · Divide moles by kilograms
m = 1.20 mol NaCl0.800 kg water = 1.50 mol/kg
Dr. Karmach

Guided example: solution

m = mol solute ÷ kg solvent
given: 1.20 mol NaCl · 800. g water · wanted: m
Step 2 · Grams → kilograms
800. g water = 0.800 kg water
1000 g = 1 kg · molality counts kilograms of the solvent
Step 3 · Divide moles by kilograms
m = 1.20 mol NaCl0.800 kg water = 1.50 mol/kg
0.800 kg of water holds 1.20 mol, so a full kilogram holds more: 1.50 mol. 1.50 m ✓
Dr. Karmach

Guided example: the route on the map

m = mol solute ÷ kg solvent
given: 1.20 mol NaCl · 800. g water · found: 1.50 mol/kg

The salt came in moles, so no molar mass. Two moves: grams to kilograms, then moles ÷ kilograms. ✓
Dr. Karmach

Practice 1

fruit syrup: fructose (C₆H₁₂O₆) dissolved in water
given: 0.840 mol fructose · 600. g water · wanted: m

A fruit syrup holds 0.840 mol of fructose in 600. g of water. What is its molality?

  1. 0.504
  2. 1.40 × 10⁻³
  3. 1.40
  4. 0.714
Dr. Karmach

Practice 1 answer: C

m = mol solute ÷ kg solvent
given: 0.840 mol fructose · 600. g water · wanted: m
600. g water = 0.600 kg water · m = 0.840 mol fructose0.600 kg water = 1.40 mol/kg · answer C

A multiplied instead of dividing: 0.840 × 0.600 = 0.504. B divided by grams of water: 0.840 ÷ 600 = 1.40 × 10⁻³, 1000 times too small. D flipped the fraction: 0.600 ÷ 0.840 = 0.714 counts kilograms per mole.

More moles than kilograms, so the molality tops 1: 0.600 kg carries 0.840 mol, a full kilogram 1.40 mol ✓
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

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.
Dr. Karmach

Practice 2

hand-lotion base: glycerol (C₃H₈O₃) dissolved in water
molar mass: glycerol 92.09 g/mol

A lotion base holds 46.0 g of glycerol in 400. g of water. What is the molality of the glycerol?

  1. 1.25
  2. 1.12
  3. 115
  4. 0.00125
Dr. Karmach

Practice 2 answer: A

m = mol solute ÷ kg solvent
given: 46.0 g glycerol (92.09 g/mol) · 400. g water · wanted: m
46.0 g glycerol × 1 mol glycerol92.09 g glycerol = 0.500 mol · 400. g water = 0.400 kg water
m = 0.500 mol glycerol0.400 kg water = 1.25 mol/kg · answer A

B used the solution's mass: 0.500 mol ÷ 0.446 kg = 1.12. C skipped the molar mass: 46.0 g ÷ 0.400 kg = 115. D divided by grams of water: 0.500 ÷ 400 = 0.00125 mol/g, 1000 times too small.

0.400 kg of water carries 0.500 mol, so a full kilogram carries 2.5 times that: 1.25 mol ✓
Dr. Karmach

Worked example 2: 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 2: 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 2: 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 2: 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 2: 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 2: 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

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 3

de-icing fluid: propylene glycol (C₃H₈O₂) in water
molar mass: propylene glycol 76.09 g/mol

A de-icing fluid must be 1.60 m propylene glycol, made with 750. g of water. What mass of propylene glycol dissolves, in grams?

  1. 1.20
  2. 91.3
  3. 35.7
  4. 9.13 × 10⁴
Dr. Karmach

Practice 3 answer: B

m = mol solute ÷ kg solvent
given: 1.60 m propylene glycol (76.09 g/mol) · 750. g water · wanted: g propylene glycol
0.750 kg water × 1.60 mol1 kg water × 76.09 g1 mol = 91.3 g · answer B

A stopped at moles: 0.750 × 1.60 = 1.20 mol. C divided the kilograms by the molality: 0.750 ÷ 1.60 = 0.469 mol, then × 76.09 = 35.7. D kept the water in grams: 750 × 1.60 × 76.09 = 9.13 × 10⁴.

Three quarters of a kilogram takes three quarters of 1.60 mol: 1.20 mol, and 1.20 mol × 76.09 g/mol = 91.3 g ✓
Dr. Karmach

Practice 4

aqueous sodium hydroxide (NaOH)
molar mass: NaOH 40.00 g/mol

How many grams of water dissolve 8.00 g of NaOH to make a 0.500 m solution?

  1. 100.
  2. 1.60 × 10⁴
  3. 0.400
  4. 400.
Dr. Karmach

Practice 4 answer: D

0.500 m NaOH: 0.500 mol NaOH = 1 kg water
given: 8.00 g NaOH (40.00 g/mol) · wanted: g water · three conversion factors
8.00 g NaOH × 1 mol NaOH40.00 g NaOH = 0.200 mol NaOH
0.200 mol NaOH × 1 kg water0.500 mol NaOH × 1000 g water1 kg water = 400. g water · answer D

A flipped the molality factor: 0.200 × 0.500 = 0.100 kg, or 100. g. B skipped the molar mass: 8.00 ÷ 0.500 = 16.0 kg, or 1.60 × 10⁴ g. C stopped at 0.400 kg.

A full kilogram carries 0.500 mol, so 0.200 mol needs 0.400 kg: 400. g ✓
Dr. Karmach

Practice 4: the route on the map

0.500 m NaOH: 0.500 mol NaOH = 1 kg water
given: 8.00 g NaOH · found: 400. g water

Three moves: grams to moles, the molality flipped to carry moles to kilograms, then kilograms to grams. ✓
Dr. Karmach

Practice 5

aqueous potassium chloride (KCl)
molar mass: KCl 74.55 g/mol

A solution holds 37.3 g of KCl in enough water to make a total mass of 287.3 g. What is the molality of the KCl?

  1. 1.74
  2. 0.500
  3. 1.54
  4. 2.00 × 10⁻³
  5. 2.00
Dr. Karmach

Practice 5 answer: E

m = mol solute ÷ kg solvent
given: 37.3 g KCl (74.55 g/mol) · 287.3 g solution · wanted: m
287.3 g solution − 37.3 g KCl = 250.0 g water = 0.2500 kg water
37.3 g KCl × 1 mol KCl74.55 g KCl = 0.500 mol · m = 0.500 mol0.2500 kg = 2.00 mol/kg · answer E

A used the solution's mass: 0.500 ÷ 0.2873 = 1.74. B stopped at moles. C added the KCl to a total that already held it: 0.500 ÷ 0.3246 = 1.54. D divided by grams: 0.500 ÷ 250.0 = 2.00 × 10⁻³.

A quarter kilogram of water carries 0.500 mol, so a full kilogram carries four times that: 2.00 mol ✓
Dr. Karmach

Practice 5: the route on the map

m = mol solute ÷ kg solvent
given: 37.3 g KCl · 287.3 g solution · found: 2.00 mol/kg

Four moves: the KCl leaves the total to give the water, the water becomes kilograms, the KCl becomes moles, then moles ÷ kilograms. ✓
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 2.0 m solution is warmed from 20 °C to 60 °C. Is it still 2.0 m? Explain with mass and volume.

Molarity counts moles per liter of solution; molality counts moles per kilogram of solvent. Molality returns in freezing-point and boiling-point changes, where the shift grows with the solute's moles per kilogram of solvent.

Dr. Karmach

8 · 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

Four properties that count particles

A colligative property depends only on how many solute particles dissolve, not which ones. Osmotic pressure is the push needed to stop water from crossing a membrane into a solution.

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

The route to a freezing or boiling point

A problem lights one path through the four columns. A ranking question compares i × m. A question that asks for ΔT stops after step 3.

Dr. Karmach

Guided example: which boils higher?

ΔTb = i · Kb · m
given: 0.800 m glucose, C₆H₁₂O₆ · 0.800 m KBr · both in water · wanted: the solution with the higher boiling point

Two pots of water each hold 0.800 m of solute: glucose in one, potassium bromide in the other. Which boils at the higher temperature?

Three moves: count the particles, multiply by the molality, compare.

Dr. Karmach

Guided example: solution

ΔTb = i · Kb · m
0.800 m glucose · 0.800 m KBr · same water, same Kb = 0.512 °C·kg/mol

Step 1 · Count the particles

glucose: molecular, dissolves whole · KBr: K⁺ + Br⁻
glucose i = 1 · KBr i = 2
Dr. Karmach

Guided example: solution

ΔTb = i · Kb · m
0.800 m glucose · 0.800 m KBr · same water, same Kb = 0.512 °C·kg/mol
Step 1 · Count the particles
glucose: molecular, dissolves whole · KBr: K⁺ + Br⁻
glucose i = 1 · KBr i = 2
Compare the particle counts
glucose: 1 × 0.800 m = 0.800 · KBr: 2 × 0.800 m = 1.60
moles of dissolved particles per kg of water

Same water, same Kb. KBr puts twice the particles in the water, so its boiling point rises twice as far.

Dr. Karmach

Guided example: solution

ΔTb = i · Kb · m
0.800 m glucose · 0.800 m KBr · same water, same Kb = 0.512 °C·kg/mol
Step 1 · Count the particles
glucose: molecular, dissolves whole · KBr: K⁺ + Br⁻
glucose i = 1 · KBr i = 2
Compare the particle counts
glucose: 1 × 0.800 m = 0.800 · KBr: 2 × 0.800 m = 1.60
moles of dissolved particles per kg of water
Check with the equation: glucose 1 × 0.512 × 0.800 = 0.410 °C, KBr 2 × 0.512 × 0.800 = 0.819 °C. KBr boils higher: 100.82 °C against 100.41 °C. ✓
Dr. Karmach

Guided example: the route on the map

KBr: 2 × 0.800 = 1.60 · glucose: 1 × 0.800 = 0.800
given: 0.800 m each · found: KBr boils higher

A ranking needs only i × m. The same K cancels out of the comparison. ✓
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
Kf = 1.86 °C·kg/mol for every solution below

Three solutions are each 0.40 m in water. Which one has the lowest freezing point?

  1. sucrose, C₁₂H₂₂O₁₁
  2. calcium chloride, CaCl₂
  3. potassium nitrate, KNO₃
  4. all three freeze at the same temperature
Dr. Karmach

Practice 1 answer: B

i × m: sucrose 1 × 0.40 = 0.40 · KNO₃ 2 × 0.40 = 0.80 · CaCl₂ 3 × 0.40 = 1.20
CaCl₂ gives Ca²⁺ + 2 Cl⁻: the most particles · the lowest freezing point · answer B

A judged by the size of the molecule: sucrose's 45 atoms stay together as one particle, so i = 1. C split the nitrate into atoms, 1 + 1 + 3 = 5 pieces; a polyatomic ion stays whole, so KNO₃ gives K⁺ and NO₃⁻, i = 2. D ignored i: equal molality is not equal particle count; 0.40 m of CaCl₂ is 1.20 mol/kg of particles.

1.20 mol/kg of particles is the most, so CaCl₂ freezes lowest, near 0 − 3 × 1.86 × 0.40 = −2.2 °C. ✓
Dr. Karmach

Practice 1: the route on the map

CaCl₂ 1.20 > KNO₃ 0.80 > sucrose 0.40
given: 0.40 m each · found: CaCl₂ freezes lowest

The guided example's route: count, multiply by m, compare. ✓
Dr. Karmach

Practice 2

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 2 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

Practice 2: the route on the map

ΔTf = 2 × 1.86 × 0.900 = 3.35 °C
KCl gives K⁺ + Cl⁻: i = 2 · m given · the change is asked: stop at ΔTf

The route of worked example 2, with KCl's two ions. ✓
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

Your turn: the route on the map

ΔTb = 3 × 0.512 × 1.00 = 1.54 °C → 101.54 °C
MgCl₂: i = 3 · m given · boiling uses Kb, then 100 °C + ΔTb

Boiling swaps Kf for Kb and the minus for a plus. ✓
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 3

new freezing point = 0 °C − ΔTf
Kf = 1.86 °C·kg/mol

A lawn-fertilizer solution is 1.30 m ammonium sulfate, (NH₄)₂SO₄, in water. At what temperature, in °C, does it freeze?

  1. −7.25
  2. −4.84
  3. −2.42
  4. 7.25
  5. −2.00
Dr. Karmach

Practice 3 answer: A

(NH₄)₂SO₄ gives 2 NH₄⁺ + SO₄²⁻: i = 3
given: 1.30 m · Kf = 1.86 °C·kg/mol · each ammonium ion stays whole
ΔTf = 3 × 1.86 × 1.30 = 7.25 °C → 0 °C − 7.25 °C = −7.25 °C · answer A

B counted one NH₄⁺ and one SO₄²⁻: i = 2 gives −4.84 °C, but the 2 outside the parentheses means two ammonium ions. C forgot i: 0 − 1.86 × 1.30 = −2.42 °C. D stopped at the depression and dropped the sign: +7.25 °C is above 0 °C. E used Kb: 0 − 3 × 0.512 × 1.30 = −2.00 °C.

Three ions per formula unit push the freezing point to −7.25 °C, below pure water's 0 °C. Freezing point goes DOWN. ✓
Dr. Karmach

Practice 3: the route on the map

ΔTf = 3 × 1.86 × 1.30 = 7.25 °C → −7.25 °C
(NH₄)₂SO₄: i = 3 · m given · the freezing point is asked: shift from 0 °C

Step 1 carried the weight: the subscript outside the parentheses counts ions. ✓
Dr. Karmach

Practice 4

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 4 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

Practice 4: the route on the map

36.4 g BaCl₂ → 0.699 m → ΔTf = 3.90 °C → −3.90 °C
BaCl₂: i = 3 · molality from grams, ÷ 0.250 kg of water · shift from 0 °C

The route of worked example 3: all four steps, in order. ✓
Dr. Karmach

Worked example 4: grams of salt for a boiling point

ΔTb = i · Kb · m, run backward
given: 1.50 kg water · target boiling point 101.00 °C · NaCl 58.44 g/mol · Kb = 0.512 °C·kg/mol · wanted: grams of NaCl

A cook wants a pot holding 1.50 kg of water to boil at 101.00 °C. Salt is the only solute. How many grams of NaCl must dissolve?

Run the route backward: undo the shift, undo the multiplication, then turn molality into grams.

Dr. Karmach

Worked example 4: solution

ΔTb = i · Kb · m, run backward
1.50 kg water · target 101.00 °C · NaCl 58.44 g/mol · Kb = 0.512 °C·kg/mol

Step 1 · Count the particles

NaCl dissolves into Na⁺ and Cl⁻, so i = 2.

Dr. Karmach

Worked example 4: solution

ΔTb = i · Kb · m, run backward
1.50 kg water · target 101.00 °C · NaCl 58.44 g/mol · Kb = 0.512 °C·kg/mol
Step 1 · Count the particles Undo the shift
ΔTb = 101.00 °C − 100.00 °C = 1.00 °C
Dr. Karmach

Worked example 4: solution

ΔTb = i · Kb · m, run backward
1.50 kg water · target 101.00 °C · NaCl 58.44 g/mol · Kb = 0.512 °C·kg/mol
Step 1 · Count the particles Undo the shift
ΔTb = 101.00 °C − 100.00 °C = 1.00 °C
Undo the multiplication
m = 1.00 °C2 × 0.512 °C·kg/mol = 0.9766 mol/kg
i = 2 and m = 0.9766 mol/kg carry into the grams. ✓
Dr. Karmach

Worked example 4: grams of salt

m = 0.9766 mol NaCl per kg of water
1.50 kg water · NaCl 58.44 g/mol · wanted: grams of NaCl

Molality to grams

Two conversion factors are needed.

1.50 kg water × 0.9766 mol NaCl1 kg water × 58.44 g NaCl1 mol NaCl = 85.6 g NaCl
Dr. Karmach

Worked example 4: grams of salt

m = 0.9766 mol NaCl per kg of water
1.50 kg water · NaCl 58.44 g/mol · wanted: grams of NaCl
Molality to grams
1.50 kg water × 0.9766 mol NaCl1 kg water × 58.44 g NaCl1 mol NaCl = 85.6 g NaCl
Check forward: 85.6 g ÷ 58.44 g/mol ÷ 1.50 kg = 0.977 m, and 2 × 0.512 × 0.9766 = 1.00 °C. A pinch of salt in the pasta pot barely moves the boiling point. ✓
Dr. Karmach

Worked example 4: the route on the map

101.00 °C → ΔTb 1.00 °C → m 0.9766 mol/kg → 1.465 mol → 85.6 g NaCl
the route run backward · i = 2 · Kb for boiling · kg of water, then molar mass

Each backward move undoes a forward one, in reverse order: subtract 100, divide by i · Kb, then use kg and molar mass. ✓
Dr. Karmach

Practice 5

ΔTf = i · Kf · m
molar mass MgCl₂ 95.21 g/mol · Kf = 1.86 °C·kg/mol

A road brine made with 600. g of water must stay liquid down to −8.50 °C. How many grams of magnesium chloride, MgCl₂, must dissolve?

  1. 0.914
  2. 261
  3. 87.0
  4. 37.5
  5. 316
Dr. Karmach

Practice 5 answer: C

ΔTf = i · Kf · m, run backward
target −8.50 °C: ΔTf = 8.50 °C · MgCl₂ gives Mg²⁺ + 2 Cl⁻: i = 3 · 600. g = 0.600 kg water
m = 8.50 °C ÷ (3 × 1.86 °C·kg/mol) = 1.523 mol/kg → 0.600 kg × 1.523 mol/kg = 0.914 mol → 0.914 mol × 95.21 g/mol = 87.0 g · answer C

A stopped at moles: 0.914 mol is one step short of grams. B forgot i: 8.50 ÷ 1.86 × 0.600 × 95.21 = 261 g. D flipped the rearrangement: (3 × 1.86) ÷ 8.50 × 0.600 × 95.21 = 37.5 g. E used Kb: 8.50 ÷ (3 × 0.512) × 0.600 × 95.21 = 316 g.

Check forward: 3 × 1.86 × 1.523 = 8.50 °C, so 87.0 g of MgCl₂ holds the freezing point at −8.50 °C. ✓
Dr. Karmach

Practice 5: the route on the map

−8.50 °C → ΔTf 8.50 °C → m 1.523 mol/kg → 0.914 mol → 87.0 g MgCl₂
the route run backward · i = 3 · Kf for freezing · kg of water, then molar mass

The backward route of worked example 4, now with Kf and a freezing target. ✓
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. The same particle count returns with acids and bases: a strong acid ionizes completely, a weak acid releases only a few ions.

Dr. Karmach

9 · Parts per Million & Parts per Billion

Calculate a solution's concentration in ppm or ppb from the masses of solute and solution, use the dilute-water shortcut 1 ppm ≈ 1 mg/L (1 ppb ≈ 1 µg/L), and use a ppm value as a conversion factor between volume of water and mass of solute.

Dr. Karmach

When a percent is far too big

A water report lists lead at 15 ppb and fluoride at 0.7 ppm, never as a percent. A solute this dilute needs a denominator bigger than a hundred.

Dr. Karmach

From mass percent to ppm

mass percent = (g solute ÷ g solution) × 100
part over the whole solution, solute plus solvent

A 400. g sample of spring water holds 0.0036 g of calcium. Find the mass percent.

Dr. Karmach

From mass percent to ppm

mass percent = (g solute ÷ g solution) × 100
part over the whole solution, solute plus solvent

A 400. g sample of spring water holds 0.0036 g of calcium. Find the mass percent.

0.0036 g calcium400. g solution × 100 = 0.00090%

A percent this small is hard to read. The same fraction × 10⁶ reads 9.0 ppm.

Dr. Karmach

Below one part in a hundred

A percent is parts per hundred. A trace solute never reaches one part in a hundred, so the same mass ratio is scaled to a larger whole.

ppm = parts per million (10⁶) · ppb = parts per billion (10⁹)
both are mass ratios: mass of solute over mass of solution: the same fraction a percent uses, times a bigger power of ten
Dr. Karmach

The two formulas

Each is the mass fraction times its power of ten. The denominator is the whole solution, solute plus solvent.

ppm = (mass solute / mass solution) × 10⁶
ppb = (mass solute / mass solution) × 10⁹, a thousand times finer

The mass units cancel, so ppm and ppb carry no unit of their own.

Dr. Karmach

The water shortcut: 1 ppm ≈ 1 mg/L

A dilute aqueous solution has density near 1.00 g/mL, so 1 L weighs about 1000 g.

1 ppm ≈ 1 mg/L · 1 ppb ≈ 1 µg/L
1 mg in 1 kg = 1 mg per 1000 g = 1 part in 10⁶ = 1 ppm; the density ≈ 1.00 g/mL is what makes L ↔ kg work. 1 ppm = 1 mg/L is given with every problem that uses it

A ppm then reads as mg/L. A dense brine or a nonaqueous solvent breaks the shortcut.

Dr. Karmach

The method

  1. Mass fraction, same units: solute mass over solution mass.
  2. Multiply by the power of ten: 10⁶ for ppm, 10⁹ for ppb.
  3. In dilute water: 1 ppm reads as 1 mg/L; mg/L × liters gives the mass.
Dr. Karmach

One route for ppm and ppb

Any solution: both masses in grams, part over whole, then one power of ten. Dilute water only: with the given 1 ppm = 1 mg/L, milligrams over liters is already ppm.

Dr. Karmach

Guided example: chromium in river water

37.0 mg chromium in a 375.0 g sample of river water
given: 37.0 mg solute · 375.0 g solution · wanted: mass percent, ppm, ppb

A 375.0 g sample of river water taken near an industrial plant contains 37.0 mg of chromium. What is the chromium concentration as a mass percent, in ppm, and in ppb?

The solute is in milligrams and the solution in grams. Match the units first.

Dr. Karmach

Guided example: solution

37.0 mg chromium in a 375.0 g sample of river water
given: 37.0 mg solute · 375.0 g solution · wanted: mass percent, ppm, ppb

Step 1 · Mass fraction, same units

Milligrams to grams, then solute over solution.

37.0 mg Cr × 1 g1000 mg = 0.0370 g Cr    0.0370 g Cr375.0 g solution = 9.87 × 10⁻⁵
Dr. Karmach

Guided example: solution

37.0 mg chromium in a 375.0 g sample of river water
given: 37.0 mg solute · 375.0 g solution · wanted: mass percent, ppm, ppb
Step 1 · Mass fraction, same units
37.0 mg Cr × 1 g1000 mg = 0.0370 g Cr    0.0370 g Cr375.0 g solution = 9.87 × 10⁻⁵
Step 2 · Multiply by the power of ten

One fraction, three powers of ten.

× 100 = 9.87 × 10⁻³ % · × 10⁶ = 98.7 ppm · × 10⁹ = 9.87 × 10⁴ ppb
each power of ten multiplies the same fraction, 9.87 × 10⁻⁵: the same chromium on three scales
Dr. Karmach

Guided example: solution

37.0 mg chromium in a 375.0 g sample of river water
given: 37.0 mg solute · 375.0 g solution · wanted: mass percent, ppm, ppb
Step 1 · Mass fraction, same units
37.0 mg Cr × 1 g1000 mg = 0.0370 g Cr    0.0370 g Cr375.0 g solution = 9.87 × 10⁻⁵
Step 2 · Multiply by the power of ten
× 100 = 9.87 × 10⁻³ % · × 10⁶ = 98.7 ppm · × 10⁹ = 9.87 × 10⁴ ppb
each power of ten multiplies the same fraction, 9.87 × 10⁻⁵: the same chromium on three scales
98.7 ppm is 9.87 × 10⁴ ppb: each step down the ladder is × 1000. The percent, 0.00987%, is the hardest of the three to read. ✓
Dr. Karmach

Guided example: the route on the map

37.0 mg chromium in a 375.0 g sample of river water
given: 37.0 mg solute · 375.0 g solution · found: 9.87 × 10⁻³ % · 98.7 ppm · 9.87 × 10⁴ ppb

Three moves: milligrams to grams, part over whole, then one power of ten for each unit. ✓
Dr. Karmach

Worked example: ppm from masses

0.0030 g copper dissolved in 250. g of water sample
given: 0.0030 g solute · 250. g solution · wanted: ppm

Old copper plumbing leaches into a 250. g water sample, adding 0.0030 g of copper. What is the copper concentration in ppm?

Both masses are already in grams: set up the mass fraction, then scale.

Dr. Karmach

Worked example: solution

Step 1 · Mass fraction, same units

0.0030 g Cu250. g solution = 1.2 × 10⁻⁵
Dr. Karmach

Worked example: solution

Step 1 · Mass fraction, same units

0.0030 g Cu250. g solution = 1.2 × 10⁻⁵
Step 2 · Multiply by the power of ten
1.2 × 10⁻⁵ × 10⁶ = 12 ppm
0.0030 / 250 × 10⁶ = 12 ppm of copper
Dr. Karmach

Worked example: solution

Step 1 · Mass fraction, same units

0.0030 g Cu250. g solution = 1.2 × 10⁻⁵
Step 2 · Multiply by the power of ten
1.2 × 10⁻⁵ × 10⁶ = 12 ppm
0.0030 / 250 × 10⁶ = 12 ppm of copper
12 ppm ≈ 12 mg/L: 12 mg of copper in each liter of this water. If you had used 10⁹ you would report 12,000 (that is ppb), and 10³ would give 0.012 (per-thousand). The ×10⁶ is what makes it ppm. ✓
Dr. Karmach

Worked example: the route on the map

0.0030 g copper dissolved in 250. g of water sample
given: 0.0030 g solute · 250. g solution · found: 12 ppm

Two moves: part over whole, then × 10⁶. No unit change was needed. ✓
Dr. Karmach

Practice 1

swordfish fillet: 1.8 × 10⁻⁴ g mercury in 200.0 g
given: 1.8 × 10⁻⁴ g solute · 200.0 g sample · wanted: ppm

A 200.0 g swordfish fillet contains 1.8 × 10⁻⁴ g of mercury. What is the mercury concentration, in ppm?

  1. 900
  2. 9.0 × 10⁻⁷
  3. 0.90
  4. 9.0 × 10⁻⁵
Dr. Karmach

Practice 1: answer C

ppm = (mass solute / mass solution) × 10⁶
1.8 × 10⁻⁴ g mercury · 200.0 g fillet · both already in grams
1.8 × 10⁻⁴ g Hg200.0 g fillet × 10⁶ = 0.90 ppm (answer C)

A used 10⁹: 1.8 × 10⁻⁴ ÷ 200.0 × 10⁹ = 900 is ppb. B stopped at the mass fraction: 1.8 × 10⁻⁴ ÷ 200.0 = 9.0 × 10⁻⁷. D used × 100: 9.0 × 10⁻⁵ is the mass percent.

0.90 mg of mercury in each kilogram of fish, just under the FDA's 1 ppm action level for mercury in fish. ✓
Dr. Karmach

Practice 1: the route on the map

swordfish fillet: 1.8 × 10⁻⁴ g mercury in 200.0 g
given: 1.8 × 10⁻⁴ g solute · 200.0 g sample · found: 0.90 ppm

Both masses were already in grams: part over whole, then × 10⁶. ✓
Dr. Karmach

Your turn: ppm as a conversion factor

fluoridated tap water: 0.70 ppm fluoride ≈ 0.70 mg/L
given: 0.70 ppm · 2.0 L of water · wanted: mg of fluoride

A city fluoridates its water to 0.70 ppm. How many milligrams of fluoride are in a 2.0 L pitcher? Read ppm as mg/L, then multiply by the volume.

2.0 L × mg F⁻1 L = mg F⁻
Dr. Karmach

Your turn: ppm as a conversion factor

fluoridated tap water: 0.70 ppm fluoride ≈ 0.70 mg/L
given: 0.70 ppm · 2.0 L of water · wanted: mg of fluoride

A city fluoridates its water to 0.70 ppm. How many milligrams of fluoride are in a 2.0 L pitcher? Read ppm as mg/L, then multiply by the volume.

2.0 L × mg F⁻1 L = mg F⁻
2.0 L × 0.70 mg F⁻1 L = 1.4 mg F⁻
Dr. Karmach

Your turn: the route on the map

fluoridated tap water: 0.70 ppm fluoride ≈ 0.70 mg/L
given: 0.70 ppm · 2.0 L of water · found: 1.4 mg F⁻

Dilute water, so the ppm reads as milligrams per liter. One factor carries liters of water to milligrams of fluoride. ✓
Dr. Karmach

How small is one ppm?

1 ppm = 1 mg in 1 kg = 1 second in ~11.6 days
1 ppb is a thousand times smaller still: about 1 second in 32 years

Use a percent for everyday concentrations (parts per hundred). Reach for ppm when the solute is a trace (dissolved minerals, fluoride, a pollutant) and ppb for the barely-there, like lead limits in drinking water.

Dr. Karmach

Where this goes wrong

Wrong power of ten. 0.0030 / 250 × 10⁹ = 12,000 is ppb, not ppm; × 10³ = 0.012 is per-thousand. ppm uses × 10⁶ → 12.
Dividing by the solvent alone. The denominator is the whole solution, solute + solvent, the same whole a percent uses.
Forgetting the volume. 0.70 ppm is 0.70 mg per liter; a 2.0 L pitcher holds 0.70 × 2.0 = 1.4 mg, not 0.70 mg.
Using the shortcut on a non-dilute or nonaqueous solution. 1 ppm ≈ 1 mg/L needs density ≈ 1.00 g/mL; a heavy brine or an organic solvent breaks 1 L ≈ 1 kg.
Dr. Karmach

Practice 2

well water: 0.84 mg nitrate in 2.40 L
given: 1 ppm = 1 mg/L for dilute water solutions

A 2.40 L jug of well water contains 0.84 mg of dissolved nitrate. What is the nitrate concentration, in ppm?

  1. 0.35
  2. 350
  3. 2.9
  4. 2.0
Dr. Karmach

Practice 2: answer A

1 ppm = 1 mg/L for dilute water solutions (given)
0.84 mg nitrate · 2.40 L of well water · wanted: ppm
0.84 mg nitrate2.40 L water = 0.35 mg/L = 0.35 ppm (answer A)

B kept milligrams over grams: 2.40 L is about 2400 g, and 0.84 ÷ 2400 × 10⁶ = 350, a thousand times too high. C flipped the fraction: 2.40 ÷ 0.84 = 2.9. D multiplied: 0.84 × 2.40 = 2.0.

Less than 1 mg spread through more than 2 L must land below 1 mg/L: 0.35 ppm. ✓
Dr. Karmach

Practice 2: the route on the map

well water: 0.84 mg nitrate in 2.40 L
given: 1 ppm = 1 mg/L · found: 0.35 ppm

Dilute water with milligrams and liters in hand: one move, milligrams over liters. ✓
Dr. Karmach

Practice 3

groundwater: 0.036 mg manganese in a 150. mL sample
given: 1 ppm = 1 mg/L for dilute water solutions

A 150. mL sample of groundwater contains 0.036 mg of manganese. What is the manganese concentration, in ppm?

  1. 240
  2. 0.0054
  3. 4.2
  4. 2.4 × 10⁻⁴
  5. 0.24
Dr. Karmach

Practice 3: answer E

1 ppm = 1 mg/L for dilute water solutions (given)
0.036 mg manganese · 150. mL of groundwater · wanted: ppm

Two conversion factors are needed.

150. mL × 1 L1000 mL = 0.150 L    0.036 mg Mn0.150 L water = 0.24 ppm (answer E)

A kept milligrams over grams: 150. mL is about 150. g, and 0.036 ÷ 150. × 10⁶ = 240. B multiplied: 0.036 × 0.150 = 0.0054. C flipped: 0.150 ÷ 0.036 = 4.2. D skipped milliliters to liters: 0.036 ÷ 150. = 2.4 × 10⁻⁴.

A liter is about 6.67 times 150. mL, so a full liter of this water holds 0.036 × 6.67 = 0.24 mg. ✓
Dr. Karmach

Practice 3: the route on the map

groundwater: 0.036 mg manganese in a 150. mL sample
given: 1 ppm = 1 mg/L · found: 0.150 L · 0.24 ppm

Two moves: milliliters to liters first, then milligrams over liters. ✓
Dr. Karmach

Practice 4

lake water: 0.024 mg lead in a 1.50 kg sample
given: 0.024 mg solute · 1.50 kg solution · wanted: ppb

A 1.50 kg sample of lake water contains 0.024 mg of lead. What is the lead concentration, in ppb?

  1. 0.016
  2. 1.6 × 10⁻⁸
  3. 1.6 × 10⁻⁶
  4. 16
Dr. Karmach

Practice 4: answer D

ppb = (mass solute / mass solution) × 10⁹
0.024 mg = 2.4 × 10⁻⁵ g lead · 1.50 kg = 1500 g solution · both in grams first
2.4 × 10⁻⁵ g Pb1500 g solution × 10⁹ = 16 ppb (answer D)

A used 10⁶: 0.016 is the same lead in ppm. B stopped at the mass fraction: 2.4 × 10⁻⁵ ÷ 1500 = 1.6 × 10⁻⁸. C used × 100: 1.6 × 10⁻⁶ is the mass percent.

16 ppb sits just above the 15 ppb action level set for lead in drinking water. ✓
Dr. Karmach

Practice 4: the route on the map

lake water: 0.024 mg lead in a 1.50 kg sample
given: 0.024 mg solute · 1.50 kg solution · found: 16 ppb

Four moves: milligrams to grams, kilograms to grams, part over whole, then × 10⁹ for ppb. ✓
Dr. Karmach

Practice 5

A 160.0 mL sample of fruit-juice concentrate contains 4.16 mg of dissolved tin. The concentrate has a density of 1.30 g/mL. What is the tin concentration in ppm?

  1. 2.00 × 10⁻⁵
  2. 20.0
  3. 26.0
  4. 33.8
Dr. Karmach

Practice 5: answer B

160.0 mL × 1.30 g/mL = 208.0 g solution · 4.16 mg = 0.00416 g tin
1 ppm ≈ 1 mg/L needs a density near 1.00 g/mL; this concentrate is 1.30 g/mL
0.00416 g tin208.0 g solution × 10⁶ = 20.0 ppm (answer B)

A stopped at the mass fraction: 0.00416 ÷ 208.0 = 2.00 × 10⁻⁵, never scaled by 10⁶. C used the water shortcut: 4.16 mg ÷ 0.1600 L = 26.0 mg/L, read as ppm; that needs 1 L ≈ 1 kg. D flipped the density: 160.0 ÷ 1.30 = 123 g, and 0.00416 ÷ 123 × 10⁶ = 33.8.

A dense liquid packs more grams into each mL, so the same tin sits in more solution mass: 20.0 ppm, below the shortcut's 26.0. ✓
Dr. Karmach

Practice 5: the route on the map

4.16 mg tin in 160.0 mL of concentrate · density 1.30 g/mL
given: 4.16 mg solute · 160.0 mL solution · found: 0.00416 g · 208.0 g · 20.0 ppm

Not dilute water, so the mass route: milligrams to grams, milliliters to grams through the density, part over whole, then × 10⁶. ✓
Dr. Karmach

Check yourself

  1. A 500. g water sample holds 0.010 g of iron. What is the iron concentration in ppm?
  2. A pond is treated to 2.5 ppm of a chemical. How many milligrams are in 4.0 L of pond water? State the shortcut you used.

The same mass fraction runs through percent, ppm, and ppb: only the power of ten shifts with how dilute the solute is. Next, a solution's volume and molarity carry through a balanced equation: solution stoichiometry.

Dr. Karmach

10 · Solution Stoichiometry

Convert a volume of solution to moles with molarity, cross substances with the mole ratio, and finish in grams or in the volume of a second solution.

Dr. Karmach

Dosed by volume

A pool is chlorinated by pumping in a measured volume of chlorine solution. Nothing is weighed: the strength on the drum's label and the liters pumped set the chlorine dose.

Dr. Karmach

Molarity as a conversion factor

1.50 M HCl: 1.50 mol HCl = 1 L of solution
liters → moles: mol over L · moles → liters: L over mol

A solution's volume and molarity give the moles of a reactant or product. Either orientation works:

1.50 mol HCl1 L soln or 1 L soln1.50 mol HCl

What volume carries 3.00 mol HCl?

Dr. Karmach

Molarity as a conversion factor

1.50 M HCl: 1.50 mol HCl = 1 L of solution
liters → moles: mol over L · moles → liters: L over mol

A solution's volume and molarity give the moles of a reactant or product. Either orientation works:

1.50 mol HCl1 L soln or 1 L soln1.50 mol HCl

What volume carries 3.00 mol HCl?

3.00 mol HCl × 1 L soln1.50 mol HCl = 2.00 L soln

The mole ratio then crosses to another substance.

Dr. Karmach

A solution's label counts moles

0.500 M NaOH: 0.500 mol NaOH = 1 L of solution
the label states a rate: moles delivered per liter poured

Measure a volume, and the label converts it to moles; the liters cancel:

0.2000 L soln × 0.500 mol NaOH1 L soln = 0.100 mol NaOH

A graduated cylinder now counts moles. No balance is needed.

Dr. Karmach

Two ways to deliver 0.100 mol

A reaction receives 0.100 mol either way. Stoichiometry works on moles; where they came from never enters the calculation.

Dr. Karmach

Volume joins the map

Volume of solution enters through molarity, exactly where grams enter through molar mass. Every route still crosses the mole bridge, and the mole ratio still switches substances.

Dr. Karmach

The method

  1. Volume → moles: mL to L, then molarity. For grams, the molar mass.
  2. Moles → moles: cross substances with the mole ratio. No other step can.
  3. Moles → the wanted unit: molar mass for grams; molarity for volume.
Dr. Karmach

Guided example: silver chloride

AgNO₃ + NaCl → AgCl + NaNO₃
given: 0.500 L of 0.100 M NaCl · wanted: mol AgCl

Silver nitrate solution is added to 0.500 L of 0.100 M NaCl until no more white AgCl forms. How many moles of AgCl precipitate?

Check each method step in turn. The volume is already in liters.

Dr. Karmach

Guided example: solution

AgNO₃ + NaCl → AgCl + NaNO₃
given: 0.500 L of 0.100 M NaCl · wanted: mol AgCl

Two conversion factors are needed.

Step 1 · Volume → moles

No mL → L hop: the volume is already 0.500 L. The molarity, 0.100 mol per liter, converts it to 0.0500 mol NaCl.

Dr. Karmach

Guided example: solution

AgNO₃ + NaCl → AgCl + NaNO₃
given: 0.500 L of 0.100 M NaCl · wanted: mol AgCl
Step 1 · Volume → moles Step 2 · Moles → moles

The mole ratio, written AgCl over NaCl (1 : 1), crosses substances; mol NaCl cancels:

0.500 L soln × 0.100 mol NaCl1 L soln × 1 mol AgCl1 mol NaCl = 0.0500 mol AgCl
Dr. Karmach

Guided example: solution

AgNO₃ + NaCl → AgCl + NaNO₃
given: 0.500 L of 0.100 M NaCl · wanted: mol AgCl
Step 1 · Volume → moles Step 2 · Moles → moles
0.500 L soln × 0.100 mol NaCl1 L soln × 1 mol AgCl1 mol NaCl = 0.0500 mol AgCl
Step 3 · Moles → the wanted unit

Moles of AgCl were wanted. No third factor is needed.

Dr. Karmach

Guided example: solution

AgNO₃ + NaCl → AgCl + NaNO₃
given: 0.500 L of 0.100 M NaCl · wanted: mol AgCl
Step 1 · Volume → moles Step 2 · Moles → moles
0.500 L soln × 0.100 mol NaCl1 L soln × 1 mol AgCl1 mol NaCl = 0.0500 mol AgCl
Step 3 · Moles → the wanted unit
One NaCl gives one AgCl, so the moles pass through the ratio unchanged: 0.0500 mol NaCl → 0.0500 mol AgCl ✓
Dr. Karmach

Guided example: the route on the map

AgNO₃ + NaCl → AgCl + NaNO₃
given: 0.500 L of 0.100 M NaCl · found: 0.0500 mol AgCl

A is NaCl, B is AgCl. The volume was already in liters, so the route starts at L of solution A: arrow 1 is the molarity, arrow 2 the mole ratio. ✓
Dr. Karmach

Practice 1

CaCl₂ + Na₂CO₃ → CaCO₃ + 2 NaCl

Hard-water scale is calcium carbonate. A lab mixes 40.0 mL of 0.250 M Na₂CO₃ with excess CaCl₂. How many moles of CaCO₃ precipitate?

  1. 0.0200
  2. 0.0100
  3. 0.160
  4. 10.0
Dr. Karmach

Practice 1: answer B

CaCl₂ + Na₂CO₃ → CaCO₃ + 2 NaCl
given: 40.0 mL of 0.250 M Na₂CO₃ · wanted: mol CaCO₃
0.0400 L soln × 0.250 mol Na₂CO₃1 L soln × 1 mol CaCO₃1 mol Na₂CO₃ = 0.0100 mol CaCO₃ (answer B)

A read NaCl's coefficient for CaCO₃: 0.0100 × 2 = 0.0200. C inverted the molarity: 0.0400 ÷ 0.250 = 0.160. D fed milliliters to the molarity: 40.0 × 0.250 = 10.0.

One CaCO₃ forms per Na₂CO₃, so the 1 : 1 ratio leaves the moles unchanged: 0.0100 mol ✓
Dr. Karmach

Practice 1: the route on the map

CaCl₂ + Na₂CO₃ → CaCO₃ + 2 NaCl
given: 40.0 mL of 0.250 M Na₂CO₃ · found: 0.0100 mol CaCO₃

A is Na₂CO₃, B is CaCO₃. Step 1 is two arrows: mL → L, then the molarity. D skipped the first one and fed milliliters to the molarity. ✓
Dr. Karmach

Worked example 1: moles from a solution volume

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂

Zinc metal dissolves in hydrochloric acid, releasing hydrogen gas. 250.0 mL of 0.400 M HCl reacts completely with excess zinc. How many moles of H₂ form?

Write the route first: mL → L → mol HCl → mol H₂.

Dr. Karmach

Worked example 1: solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂

Two conversion factors are needed.

Step 1 · Volume → moles

250.0 mL is 0.2500 L. The label's molarity converts the liters to moles of HCl:

0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Dr. Karmach

Worked example 1: solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂
Step 1 · Volume → moles
0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Step 2 · Moles → moles

The mole ratio, written H₂ over HCl (1 : 2), crosses substances; mol HCl cancels:

0.2500 L soln × 0.400 mol HCl1 L soln × 1 mol H₂2 mol HCl = 0.0500 mol H₂
Dr. Karmach

Worked example 1: solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂
Step 1 · Volume → moles
0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Step 2 · Moles → moles
0.2500 L soln × 0.400 mol HCl1 L soln × 1 mol H₂2 mol HCl = 0.0500 mol H₂
Each H₂ consumes two HCl, so the mole count halves: 0.100 mol HCl → 0.0500 mol H₂ ✓
Dr. Karmach

Worked example 1: the route on the map

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · found: 0.0500 mol H₂

A is HCl, B is H₂. Moles were wanted, so the route stops at mol B after the mole ratio. ✓
Dr. Karmach

Practice 2

Na₃PO₄ + 3 AgNO₃ → Ag₃PO₄ + 3 NaNO₃

Excess sodium phosphate precipitates the silver in 60.0 mL of 0.150 M AgNO₃ as yellow Ag₃PO₄. How many moles of Ag₃PO₄ form?

  1. 0.00900
  2. 0.0270
  3. 0.00300
  4. 3.00
Dr. Karmach

Practice 2: answer C

Na₃PO₄ + 3 AgNO₃ → Ag₃PO₄ + 3 NaNO₃
given: 60.0 mL of 0.150 M AgNO₃ · wanted: mol Ag₃PO₄
0.0600 L soln × 0.150 mol AgNO₃1 L soln × 1 mol Ag₃PO₄3 mol AgNO₃ = 0.00300 mol Ag₃PO₄ (answer C)

A skipped the mole ratio: 0.0600 × 0.150 = 0.00900 mol is the AgNO₃. B inverted the ratio: 0.00900 × 3 = 0.0270. D fed milliliters to the molarity: 60.0 × 0.150 ÷ 3 = 3.00.

Three AgNO₃ make one Ag₃PO₄, so the moles drop to a third: 0.00900 → 0.00300 mol ✓
Dr. Karmach

Practice 2: the route on the map

Na₃PO₄ + 3 AgNO₃ → Ag₃PO₄ + 3 NaNO₃
given: 60.0 mL of 0.150 M AgNO₃ · found: 0.00300 mol Ag₃PO₄

A is AgNO₃, B is Ag₃PO₄. A stopped at mol A and never crossed arrow 2; B crossed it upside down; D skipped the mL → L hop. ✓
Dr. Karmach

Worked example 2: grams of product from a solution volume

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂

Two clear solutions mix, and bright yellow lead(II) iodide settles out. 150.0 mL of 0.300 M KI reacts completely with excess Pb(NO₃)₂. What mass of PbI₂ forms? (PbI₂ 461.0 g/mol)

A tempting shortcut: carry the moles of KI straight to grams of PbI₂. Test it against the equation.

Dr. Karmach

Worked example 2: solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)

Three conversion factors are needed.

Step 1 · Volume → moles

150.0 mL is 0.1500 L. The molarity, 0.300 mol per liter, converts the liters to 0.0450 mol KI.

Dr. Karmach

Worked example 2: solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗

mol KI cannot cancel mol PbI₂. The equation makes one PbI₂ from two KI; the mole ratio must cross first.

Dr. Karmach

Worked example 2: solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗
Step 2 · Moles → moles Step 3 · Moles → the wanted unit

The ratio, written PbI₂ over KI (1 : 2), crosses substances; the molar mass then converts out:

0.1500 L soln × 0.300 mol KI1 L soln × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 10.4 g PbI₂
Dr. Karmach

Worked example 2: solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗
Step 2 · Moles → moles Step 3 · Moles → the wanted unit
0.1500 L soln × 0.300 mol KI1 L soln × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 10.4 g PbI₂
Two KI deliver one PbI₂: 0.0450 mol halves to 0.0225 mol, and each mole weighs 461.0 g: about 10 g. 10.4 g ✓
Dr. Karmach

Worked example 2: the route on the map

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · found: 10.4 g PbI₂

A is KI, B is PbI₂. The tempting shortcut jumped from mol A to grams B, but no arrow joins them: every route crosses the mole ratio. ✓
Dr. Karmach

Your turn: copper(II) hydroxide

CuSO₄ + 2 NaOH → Cu(OH)₂ + Na₂SO₄
given: 200.0 mL (0.2000 L) of 0.250 M NaOH · wanted: g Cu(OH)₂ (97.57 g/mol)

Excess copper(II) sulfate reacts with 200.0 mL of 0.250 M NaOH, and pale blue Cu(OH)₂ precipitates:

0.2000 L soln × mol NaOH1 L soln × mol Cu(OH)₂ mol NaOH × g Cu(OH)₂1 mol Cu(OH)₂ = g Cu(OH)₂

Fill the molarity, the mole ratio, and the molar mass, then compute.

Dr. Karmach

Your turn: copper(II) hydroxide

CuSO₄ + 2 NaOH → Cu(OH)₂ + Na₂SO₄
given: 200.0 mL (0.2000 L) of 0.250 M NaOH · wanted: g Cu(OH)₂ (97.57 g/mol)
0.2000 L soln × mol NaOH1 L soln × mol Cu(OH)₂ mol NaOH × g Cu(OH)₂1 mol Cu(OH)₂ = g Cu(OH)₂
0.2000 L soln × 0.250 mol NaOH1 L soln × 1 mol Cu(OH)₂2 mol NaOH × 97.57 g Cu(OH)₂1 mol Cu(OH)₂ = 2.44 g Cu(OH)₂
Dr. Karmach

Where this goes wrong

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · correct: 0.1500 L → 0.0450 mol KI → 0.0225 mol PbI₂ → 10.4 g
Feeding milliliters to the molarity. 150.0 × 0.300 = 45.0 mol KI, a thousand times too many. Molarity counts liters of solution: 150.0 mL is 0.1500 L, and 0.1500 × 0.300 = 0.0450 mol.
Skipping the mole ratio. 0.0450 × 461.0 = 20.7 g assumes one PbI₂ per KI. The equation gives 1 PbI₂ : 2 KI, and only the mole ratio switches substances.
Inverting the ratio. (2 mol KI / 1 mol PbI₂) leaves mol KI uncancelled, and 0.0450 × 2 × 461.0 = 41.5 g is wrong. Write the wanted substance on top, so the given unit cancels.
Dr. Karmach

Practice 3

FeCl₃ + 3 NaOH → Fe(OH)₃ + 3 NaCl
molar mass Fe(OH)₃ 106.87 g/mol

300.0 mL of 0.200 M NaOH reacts completely with excess iron(III) chloride, and rust-brown Fe(OH)₃ precipitates. What mass of Fe(OH)₃, in grams, forms?

  1. 2.14
  2. 6.41
  3. 19.2
  4. 0.0200
Dr. Karmach

Practice 3: answer A

FeCl₃ + 3 NaOH → Fe(OH)₃ + 3 NaCl
given: 300.0 mL of 0.200 M NaOH · wanted: g Fe(OH)₃ (106.87 g/mol)
0.3000 L soln × 0.200 mol NaOH1 L soln × 1 mol Fe(OH)₃3 mol NaOH × 106.87 g Fe(OH)₃1 mol Fe(OH)₃ = 2.14 g Fe(OH)₃ (answer A)

B skipped the mole ratio: 0.0600 × 106.87 = 6.41. C inverted the ratio: 0.0600 × 3 × 106.87 = 19.2. D stopped at moles: 0.0600 × (1/3) = 0.0200 mol Fe(OH)₃, one factor short of grams.

0.0600 mol NaOH gives a third as many moles of Fe(OH)₃: 0.0200 mol, at about 107 g per mole: about 2 g. 2.14 g ✓
Dr. Karmach

Practice 3: the route on the map

FeCl₃ + 3 NaOH → Fe(OH)₃ + 3 NaCl
given: 300.0 mL of 0.200 M NaOH · found: 2.14 g Fe(OH)₃

A is NaOH, B is Fe(OH)₃. B skipped arrow 2, the mole ratio; C ran it upside down; D stopped at mol B, one arrow short of grams. ✓
Dr. Karmach

Worked example 3: volume of a second solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 175.0 mL of 0.240 M NaOH · wanted: mL of 0.150 M H₂SO₄

A base spill of 175.0 mL of 0.240 M NaOH is neutralized with 0.150 M H₂SO₄ from the shelf. What volume of the acid solution, in milliliters, reacts completely?

Count the factors on the route: mL → L → mol NaOH → mol H₂SO₄ → L → mL.

Dr. Karmach

Worked example 3: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O

Three conversion factors are needed. Molarity works at both ends: the base's converts volume in to moles, the acid's converts moles out to volume.

Step 1 · Volume → moles

175.0 mL is 0.1750 L. The base's molarity converts the liters to moles of NaOH:

0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Dr. Karmach

Worked example 3: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles

The mole ratio, written H₂SO₄ over NaOH (1 : 2), gives 0.0210 mol H₂SO₄.

Dr. Karmach

Worked example 3: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles Step 3 · Moles → the wanted unit

The acid's molarity converts moles out to volume:

0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln × 1 mol H₂SO₄2 mol NaOH × 1 L acid soln0.150 mol H₂SO₄ = 0.140 L = 140. mL acid soln
Dr. Karmach

Worked example 3: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles Step 3 · Moles → the wanted unit
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln × 1 mol H₂SO₄2 mol NaOH × 1 L acid soln0.150 mol H₂SO₄ = 0.140 L = 140. mL acid soln
Half the moles (0.0210 vs 0.0420), but fewer per liter (0.150 vs 0.240): 140. mL is near 175.0 mL ✓
Dr. Karmach

Worked example 3: the route on the map

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 175.0 mL of 0.240 M NaOH · found: 140. mL of 0.150 M H₂SO₄

A is NaOH, B is H₂SO₄. Molarity works at both ends: the base's in, before the mole ratio, and the acid's out, after it. ✓
Dr. Karmach

Practice 4

Mg(OH)₂ + 2 HCl → MgCl₂ + 2 H₂O
molar mass Mg(OH)₂ 58.32 g/mol

An antacid tablet holds 0.450 g of Mg(OH)₂. What volume of stomach acid, 0.120 M HCl, in milliliters, does the tablet neutralize?

  1. 0.0154
  2. 64.3
  3. 32.2
  4. 0.129
  5. 129
Dr. Karmach

Practice 4: answer E

Mg(OH)₂ + 2 HCl → MgCl₂ + 2 H₂O
given: 0.450 g Mg(OH)₂ (58.32 g/mol) · wanted: mL of 0.120 M HCl
0.450 g Mg(OH)₂ × 1 mol Mg(OH)₂58.32 g Mg(OH)₂ × 2 mol HCl1 mol Mg(OH)₂ × 1 L soln0.120 mol HCl = 0.129 L = 129 mL (answer E)

A stopped at moles: 0.450 ÷ 58.32 × 2 = 0.0154 mol HCl. B skipped the mole ratio: 0.00772 ÷ 0.120 = 0.0643 L, or 64.3 mL. C inverted the ratio: 0.00772 ÷ 2 ÷ 0.120 = 0.0322 L, or 32.2 mL. D stopped at liters: 0.129 L, not yet milliliters.

Each Mg(OH)₂ takes two HCl: 0.00772 mol of base needs 0.0154 mol of acid, and at 0.120 mol per liter that is about an eighth of a liter. 129 mL ✓
Dr. Karmach

Practice 4: the route on the map

Mg(OH)₂ + 2 HCl → MgCl₂ + 2 H₂O
given: 0.450 g Mg(OH)₂ · found: 129 mL of 0.120 M HCl

A is Mg(OH)₂, B is HCl. A mass enters through the molar mass, and the volume leaves through the acid's molarity. A stopped at mol B; D stopped at L of solution B. ✓
Dr. Karmach

Practice 5

Ba(OH)₂ + 2 HCl → BaCl₂ + 2 H₂O
two labeled solutions: 0.250 M Ba(OH)₂ · 0.400 M HCl

150.0 mL of 0.250 M Ba(OH)₂ reacts completely with 0.400 M HCl. What volume of the HCl solution, in milliliters, is required?

  1. 0.0750
  2. 46.9
  3. 93.8
  4. 188
Dr. Karmach

Practice 5: answer D

Ba(OH)₂ + 2 HCl → BaCl₂ + 2 H₂O
given: 150.0 mL of 0.250 M Ba(OH)₂ · wanted: mL of 0.400 M HCl
0.1500 L base soln × 0.250 mol Ba(OH)₂1 L base soln × 2 mol HCl1 mol Ba(OH)₂ × 1 L acid soln0.400 mol HCl = 0.1875 L = 188 mL (answer D)

A stopped at moles: 0.0375 × (2/1) = 0.0750 mol HCl, one factor short of a volume. B inverted the mole ratio: 0.0375 × 1/2 ÷ 0.400 = 0.0469 L, or 46.9 mL. C skipped the mole ratio: 0.0375 ÷ 0.400 = 0.0938 L, or 93.8 mL.

Two HCl are needed per Ba(OH)₂, and the acid is not twice as concentrated (0.400 vs 0.250 M), so the acid volume comes out larger: 188 mL vs 150.0 mL ✓
Dr. Karmach

Practice 5: the route on the map

Ba(OH)₂ + 2 HCl → BaCl₂ + 2 H₂O
given: 150.0 mL of 0.250 M Ba(OH)₂ · found: 188 mL of 0.400 M HCl

A is Ba(OH)₂, B is HCl. A stopped at mol B, before the acid's molarity; B ran arrow 2 upside down; C skipped it. ✓
Dr. Karmach

Check yourself

  1. A bottle is labeled 2.00 M NaOH. Write the setup that converts 50.0 mL of this solution to moles of NaOH.
  2. In the route L of A → mol A → mol B → L of B, name the conversion factor at each arrow. Which one comes from the balanced equation?

This chain also runs backward: the volume of a known-molarity solution that reacts completely with an unknown gives the unknown's moles. That laboratory measurement is a titration.

Dr. Karmach

Can you…?

  • ☐ identify solute and solvent, write dissolving equations, and predict solubility with like dissolves like?
  • ☐ explain the dissolving process through the attractions broken and formed, and why dissolving can cool or warm the solution?
  • ☐ classify a solution as unsaturated, saturated, or supersaturated and predict how temperature and pressure (Henry's law) change solubility?
  • ☐ calculate and use molarity, percent concentration, ppm/ppb, and molality, and dilute a solution with M₁V₁ = M₂V₂?
  • ☐ carry a solution's volume and molarity through reaction stoichiometry?
  • ☐ describe the colligative properties and calculate freezing-point depression and boiling-point elevation with ΔT = i·K·m?

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

Dr. Karmach