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Solubility product Ksp notes and lesson for AP Chemistry (free PDF download)

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Solubility product Ksp notes and lesson for AP Chemistry (free PDF download)

This AP Chemistry lesson on solubility product Ksp notes gives the key ideas first, then worked examples and diagrams. After that, practise with the worksheet on solubility product Ksp and check yourself with the quiz.

Quick answer: The solubility product Ksp is the equilibrium constant for a sparingly soluble ionic solid dissolving, such as AgCl(s) ⇌ Ag⁺ + Cl⁻, with Ksp = [Ag⁺][Cl⁻]. It lets you calculate molar solubility, predict precipitation by comparing Q with Ksp, and see how common ions and pH change solubility.

Level: AP Chemistry · Curriculum: AP Chem Unit 7

Solubility product Ksp notes: the key ideas

What is the solubility product, Ksp?

Definition

For a sparingly soluble ionic solid, Ksp is the equilibrium constant for dissolving. For MₐXᵦ(s) ⇌ aM^(n+)(aq) + bX^(m−)(aq), Ksp = [M^(n+)]ᵃ[X^(m−)]ᵇ. The solid does not appear in the expression. Molar solubility s is the amount in mol that dissolves per dm³ of saturated solution.

Saturated solution of silver chloride: solid AgCl on the bottom, Ag⁺ and Cl⁻ ions in the water, and arrows showing dissolving and crystallising at equal ratessolid AgCl(s)Ag⁺Cl⁻Ag⁺Cl⁻Ag⁺Cl⁻Ag⁺Cl⁻Ag⁺Cl⁻dissolvingcrystallisingAgCl(s) ⇌ Ag⁺(aq) + Cl⁻(aq)
At saturation the two rates are equal, so the concentrations stay constant.

A saturated solution is a dynamic equilibrium: ions leave the crystal and return at the same rate. A larger Ksp, for salts with the same formula type, means a more soluble salt.

SaltDissolving equationKsp expressionKsp in terms of s
AgClAgCl ⇌ Ag⁺ + Cl⁻[Ag⁺][Cl⁻]s²
CaF₂CaF₂ ⇌ Ca²⁺ + 2F⁻[Ca²⁺][F⁻]²4s³
Ag₂CrO₄Ag₂CrO₄ ⇌ 2Ag⁺ + CrO₄²⁻[Ag⁺]²[CrO₄²⁻]4s³
Ca₃(PO₄)₂Ca₃(PO₄)₂ ⇌ 3Ca²⁺ + 2PO₄³⁻[Ca²⁺]³[PO₄³⁻]²108s⁵

How do you find solubility from Ksp?

Worked example 1

Find the molar solubility and mass solubility of AgCl (Ksp = 1.8 × 10⁻¹⁰, M = 143.3 g/mol). Ksp = s², so s = √(1.8 × 10⁻¹⁰) = 1.34 × 10⁻⁵ mol/dm³. Mass = 1.34 × 10⁻⁵ × 143.3 = 1.92 mg/dm³.

Worked example 2

Find s for CaF₂, Ksp = 3.5 × 10⁻¹¹. Each unit gives one Ca²⁺ and two F⁻, so [Ca²⁺] = s and [F⁻] = 2s. Ksp = s(2s)² = 4s³, so s = ³√(3.5 × 10⁻¹¹ / 4) = ³√(8.75 × 10⁻¹²) = 2.06 × 10⁻⁴ mol/dm³.

Key rule

To compare Q with Ksp: if Q < Ksp the solution is unsaturated, if Q = Ksp it is saturated, and if Q > Ksp a precipitate forms. Q has the same form as Ksp but uses the concentrations present right now, after mixing.

How does the common ion effect change solubility?

Adding a solution that contains one of the salt’s ions pushes the equilibrium to the left, in line with Le Chatelier’s principle. The salt becomes less soluble. When the added ion concentration is large, it is almost equal to the total concentration of that ion, so the other ion’s concentration equals s.

Bar chart of the solubility of silver chloride as minus log of molar solubility: 1.3 times ten to the minus five in pure water, falling to 1.8 times ten to the minus nine in 0.1 mol per dm cubed sodium chloride0246810−log₁₀ s (larger = less soluble)s = 1.3 × 10⁻⁵pure waters = 1.8 × 10⁻⁷0.001 mol/dm³ NaCls = 1.8 × 10⁻⁸0.01 mol/dm³ NaCls = 1.8 × 10⁻⁹0.1 mol/dm³ NaClsolvent used for AgCl
The common ion Cl⁻ lowers the molar solubility of AgCl (Ksp = 1.8 × 10⁻¹⁰).
Worked example 3

Find s for AgCl in 0.10 mol/dm³ NaCl. Here [Cl⁻] ≈ 0.10 mol/dm³, so [Ag⁺] = s = Ksp/[Cl⁻] = 1.8 × 10⁻¹⁰ / 0.10 = 1.8 × 10⁻⁹ mol/dm³. That is 7454 times smaller than in pure water.

Why does pH change the solubility?

If the anion is basic, H₃O⁺ removes it from solution and pulls the equilibrium to the right. Hydroxides, carbonates, phosphates and fluorides therefore dissolve better in acid, while chlorides, bromides and iodides of silver do not. For a hydroxide, a lower pH means a lower [OH⁻] and a higher s.

Graph of log of molar solubility of magnesium hydroxide against pH in a buffered solution: a straight line falling from about 0.7 at pH 8 to about minus 7.3 at pH 12, so it is far more soluble in acidic solutions89101112−8−6−4−20pH of buffered solutionlog₁₀ spH 10.00: s = 5.6 × 10⁻⁴
Mg(OH)2 dissolves far better as pH falls: s = Ksp / [OH⁻]².
Worked example 4

Mg(OH)₂ has Ksp = 5.6 × 10⁻¹². In pure water s = ³√(Ksp/4) = 1.12 × 10⁻⁴ mol/dm³, so [OH⁻] = 2.24 × 10⁻⁴ mol/dm³ and pH = 10.35. In a buffer at pH 10.00, [OH⁻] = 1.0 × 10⁻⁴ mol/dm³, so s = Ksp/[OH⁻]² = 5.6 × 10⁻⁴ mol/dm³, five times larger.

Common mistake

Students write s = √Ksp for every salt. That works only for salts with a 1:1 ratio such as AgCl or BaSO₄. For CaF₂ or Ag₂CrO₄ use 4s³, and always write the Ksp expression first. Also do not compare Ksp values of salts with different formulas to rank solubility.

Lina’s tip

Use a three-line ICE table for every Ksp problem: write the dissolving equation, put s (or 2s, 3s) under each ion and substitute into the Ksp expression. Check at the end by multiplying the ion concentrations again.

Key points to remember
  • Ksp = product of ion concentrations (each raised to its coefficient) at saturation; the solid is omitted.
  • Molar solubility: AB gives s = √Ksp; AB₂ and A₂B give s = ³√(Ksp/4).
  • Precipitation: Q > Ksp precipitate forms; Q = Ksp saturated; Q < Ksp unsaturated.
  • A common ion lowers solubility, as in s = Ksp/[Cl⁻] for AgCl in NaCl.
  • Salts of basic anions (OH⁻, CO₃²⁻, F⁻, PO₄³⁻) dissolve better in acid.

Ksp, precipitation and the common ion effect: frequently asked questions

What is the difference between solubility and Ksp?

Solubility is the amount that dissolves in a given volume, often written as molar solubility s in mol/dm³. Ksp is the equilibrium constant that links the ion concentrations at saturation. You can convert between them with the dissolving equation.

Why is the solid left out of the Ksp expression?

The concentration of a pure solid is constant, so it is absorbed into the constant. Only dissolved ions appear in Ksp.

How do you know whether a precipitate forms?

Calculate Q from the concentrations after mixing, remembering that volumes add. If Q is greater than Ksp, a precipitate forms until Q falls to Ksp.

Why does a common ion reduce solubility?

The extra ion shifts the dissolving equilibrium to the left, so more solid stays undissolved. The shift is a direct Le Chatelier effect and Ksp itself does not change.

Why does CaCO₃ dissolve in acid?

The carbonate ion reacts with H₃O⁺ to form CO₂ and water, which removes CO₃²⁻ from the equilibrium. The solid then dissolves to replace it.

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