Solubility product
For sparingly soluble salt M_aX_b ⇌ aM⁺ + bX⁻: K_sp = [M⁺]^a[X⁻]^b. Q < K_sp: more dissolves. Q > K_sp: precipitates. Q = K_sp: saturated.
-- NCERT Class 11 Chemistry, Ch. 6, p. 38The trap that costs marks in Ksp problems is almost always the same: forgetting stoichiometric powers. For a salt like CaF₂, students write Ksp = [Ca²⁺][F⁻] instead of Ksp = [Ca²⁺][F⁻]². That single missing exponent turns every downstream calculation wrong and hands away 4 marks under negative marking.
What Ksp actually is. When a sparingly soluble salt MₐXᵦ is placed in water, a tiny amount dissolves and establishes an equilibrium:
MₐXᵦ(s) ⇌ aM⁺(aq) + bX⁻(aq)
The solubility product is the equilibrium constant for this process (NCERT Class 11 Chemistry Chapter 7, page 38):
Ksp = [M⁺]ᵃ · [X⁻]ᵇ
The solid does not appear — its activity is 1 by convention.
Connecting solubility (s) to Ksp. If the molar solubility is s, then [M⁺] = as and [X⁻] = bs. For a 1:1 salt like AgCl: Ksp = s². For a 1:2 salt like CaF₂: Ksp = (s)(2s)² = 4s³. For a 2:1 salt like Ag₂CrO₄: Ksp = (2s)²(s) = 4s³. The stoichiometry changes the algebraic form entirely.
Predicting precipitation. Compare the ionic product Q with Ksp:
Common-ion effect. Adding a common ion (say, F⁻ from NaF to a saturated CaF₂ solution) increases [F⁻], pushing Q above Ksp. The system responds by precipitating CaF₂ until Q falls back to Ksp. This lowers the effective solubility of the salt.
Watch out: when a problem gives you a non-1:1 salt and asks for solubility, write the dissolution equation first, assign stoichiometric coefficients to s, then build the Ksp expression. Skipping this step is how the stoichiometric-power trap catches you.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
The solubility product expression for Mg(OH)₂ is:
The Ksp of AgCl is 1.8 × 10⁻¹⁰. What is the molar solubility of AgCl in pure water?
For CaF₂ (Ksp = 3.2 × 10⁻¹¹), the molar solubility in pure water is closest to:
What is the SI unit of Ksp for a salt of type AB₂ (e.g., CaF₂)?
If the ionic product Q for PbCl₂ in a solution is 2.5 × 10⁻⁴ and Ksp of PbCl₂ is 1.7 × 10⁻⁵, what will happen?
The solubility of Ag₂CrO₄ in pure water is s mol/L. Its Ksp expression in terms of s is:
The Ksp of BaSO₄ is 1.1 × 10⁻¹⁰. If 0.01 M Na₂SO₄ is added to a saturated BaSO₄ solution, the new solubility of BaSO₄ is approximately:
For a sparingly soluble salt M₃(PO₄)₂ with molar solubility s, the Ksp expression is:
Pattern: NEET pattern: solubility ksp — compute solubility from Ksp for a salt with stoichiometric coefficients > 1.
Given
Ksp of Ca₃(PO₄)₂ = 2.07 × 10⁻³³. The salt is dissolved in pure water at 25°C.
Required
Find the molar solubility (s) of Ca₃(PO₄)₂ in pure water.
Concept
For a sparingly soluble salt, the dissolution equilibrium defines Ksp. The stoichiometric coefficients become powers in the Ksp expression (NCERT Class 11 Chemistry Chapter 7, page 38).
Formula
Ca₃(PO₄)₂ ⇌ 3Ca²⁺ + 2PO₄³⁻ Ksp = [Ca²⁺]³ · [PO₄³⁻]² If molar solubility = s: [Ca²⁺] = 3s, [PO₄³⁻] = 2s Ksp = (3s)³(2s)² = 27s³ · 4s² = 108s⁵
Substitution
2.07 × 10⁻³³ = 108s⁵ s⁵ = 2.07 × 10⁻³³ / 108 = 1.917 × 10⁻³⁵
Calculation
s = (1.917 × 10⁻³⁵)^(1/5) Take the fifth root: 1.917^(1/5) ≈ 1.139; (10⁻³⁵)^(1/5) = 10⁻⁷ s ≈ 1.14 × 10⁻⁷ mol/L Note on exact constants: the coefficient 108 is an exact integer derived from stoichiometry (3³ × 2² = 108). It does not limit significant figures. The answer precision is governed by the 3 significant figures in Ksp = 2.07 × 10⁻³³.
Final answer
The molar solubility of Ca₃(PO₄)₂ in pure water is approximately **1.14 × 10⁻⁷ mol/L**.
Common trap
Writing Ksp = s·s = s² (treating the salt as 1:1) or Ksp = 3s·2s = 6s² (using coefficients as multipliers without raising to powers). The correct form demands (3s)³ and (2s)², producing 108s⁵. This is the stoichiometric-power trap that appears frequently in NEET solubility-product questions.
Similar NEET-style question
The Ksp of Ag₂CrO₄ is 1.12 × 10⁻¹². Calculate its molar solubility in pure water. *(Hint: Ag₂CrO₄ ⇌ 2Ag⁺ + CrO₄²⁻, so Ksp = 4s³.)* ---
For sparingly soluble salt M_aX_b ⇌ aM⁺ + bX⁻: K_sp = [M⁺]^a[X⁻]^b. Q < K_sp: more dissolves. Q > K_sp: precipitates. Q = K_sp: saturated.
-- NCERT Class 11 Chemistry, Ch. 6, p. 38pH of acidic buffer in terms of conjugate base/acid concentrations. For basic buffer: pOH = pKb + log10([salt]/[base]).
| Symbol | Quantity | SI Unit |
|---|---|---|
| pKa | -log Ka | - |
| [salt] | conjugate base conc | mol/L |
| [acid] | weak acid conc | mol/L |
Stronger acid → weaker conjugate base, and vice versa. pKa + pKb = 14.
| Symbol | Quantity | SI Unit |
|---|---|---|
| Ka | acid dissociation | - |
| Kb | base dissociation | - |
| Kw | water 10^-14 | - |
Convert between pressure-based and concentration-based equilibrium constants. T in K; R = 0.0821 L atm/mol/K (when K_p in atm).
| Symbol | Quantity | SI Unit |
|---|---|---|
| K_p | pressure constant | - |
| K_c | concentration constant | - |
| Δn | mole change | - |
Equilibrium constant for sparingly soluble salt. Q < K_sp: dissolves; Q > K_sp: precipitates.
| Symbol | Quantity | SI Unit |
|---|---|---|
| K_sp | solubility product | - |
Logarithmic acidity scale. Pure water at 25°C: pH = 7 = pOH.
| Symbol | Quantity | SI Unit |
|---|---|---|
| [H+] | hydrogen ion conc | mol/L |
| [OH-] | hydroxide conc | mol/L |
These are the exact patterns that cause wrong answers in NEET. Each trap includes when it triggers and how to avoid it.
Category: Overthinking
Student claims catalyst shifts equilibrium toward products. Catalyst speeds up forward AND reverse equally; equilibrium position unchanged.
Question lists catalyst addition among options for shifting equilibrium.
Catalyst lowers activation energy of BOTH forward and reverse reactions equally. Time to reach equilibrium decreases; equilibrium position is unchanged.
Category: Sign Convention
Δn = (mol gas product) - (mol gas reactant). Sign matters; K_p = K_c (RT)^Δn.
Convert K_p ↔ K_c for gas-phase reaction.
Count moles of gas only (ignore solids/liquids). Δn = product - reactant. If Δn = 0, K_p = K_c. If Δn = +1, K_p = K_c × RT.
Category: Similar Terms
For salt M_aX_b: K_sp = [M⁺]^a [X⁻]^b. Student uses [M⁺][X⁻] regardless of stoichiometry.
K_sp problem with non-1:1 salt (e.g. CaF₂, Mg(OH)₂, Ag₂CrO₄).
Write dissolution: M_aX_b → aM + bX. Then K_sp = [M]^a · [X]^b. For CaF₂ ↔ Ca + 2F: K_sp = s · (2s)² = 4s³.
Root cause: concept gap
Catalyst speeds up forward AND reverse equally. Equilibrium position is unchanged. Time to reach equilibrium decreases.
Root cause: concept gap
Δn = (moles GAS product) - (moles GAS reactant). Solids and liquids excluded.
Root cause: formula misuse
For M_aX_b: K_sp = [M]^a · [X]^b. CaF₂: K_sp = s · (2s)² = 4s³.
Root cause: concept gap
Increase P → shift toward FEWER moles of gas. Decrease P → shift toward MORE moles. Reactions with same number of moles of gas: P doesn't shift equilibrium.
Root cause: concept gap
Weak acid: only fraction ionises. [H+] ≈ √(Ka · C). For 0.1 M acetic acid (Ka ~10⁻⁵): [H+] ~10⁻³ (pH ~3), not 1 (pH=1).
15 questions from NEET 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.
C [A] = [B] = [C] = 2 × 10–3 M. Then, which of the following is correct?
Amongst the given options which of the following molecules/ ion acts as a Lewis acid?
Which complex compound is most stable?
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
wrong delta n sign
Counts moles incorrectly
treats catalyst as shifting
Believes catalyst shifts equilibrium
ignores weak vs strong
Treats weak acid as fully dissociated
forgets stoichiometric coefficient power
Uses [M+]^1 [X-]^1 for M(X)_2 salt
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