Common ion effect
Suppression of ionisation of a weak electrolyte by adding a strong electrolyte with a common ion. Example: adding NaCl to NH₄OH suppresses NH₄⁺.
-- NCERT Class 11 Chemistry, Ch. 6, p. 32The common ion effect is one of the most directly tested consequences of equilibrium in NEET chemistry — and the trap is almost always the same: students forget to raise ion concentrations to their stoichiometric powers when an external source supplies a common ion.
What is the common ion effect? When a soluble salt that shares an ion with a sparingly soluble salt is added to the solution, the concentration of that shared (common) ion increases. By Le Chatelier's principle, the dissolution equilibrium shifts backward, and the solubility of the sparingly soluble salt decreases. NCERT Class 11 Chemistry Chapter 7 (Equilibrium), page 32, defines this as the suppression of ionisation or solubility caused by the presence of a common ion from a second electrolyte.
The NEET trap — stoichiometric powers in K_sp. Consider CaF₂ dissolving: CaF₂ ⇌ Ca²⁺ + 2F⁻. If solubility is s, then [Ca²⁺] = s and [F⁻] = 2s, giving K_sp = s·(2s)² = 4s³. Now add NaF (a soluble fluoride). The F⁻ concentration is no longer just 2s — it becomes (2s + C_NaF). Many students write K_sp = [Ca²⁺][F⁻] without the square on fluoride, and then apply the common ion incorrectly.
How NEET tests this: a problem gives K_sp of a non-1:1 salt and asks for its solubility in the presence of a common ion source. The correct distractor exploits the stoichiometric-power mistake — the answer you get by ignoring the exponent lands on one of the wrong options.
Watch out: the common ion effect applies only when the added ion is genuinely common to the equilibrium. Adding a non-common salt (say NaCl to a CaF₂ solution) does not suppress CaF₂ solubility via this mechanism.
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 of PbCl₂ is 1.6 × 10⁻⁵. What is the molar solubility of PbCl₂ in pure water?
What happens to the solubility of AgCl (K_sp = 1.8 × 10⁻¹⁰) when it is dissolved in 0.10 M NaCl solution instead of pure water?
The K_sp of BaSO₄ is 1.1 × 10⁻¹⁰. Its molar solubility in 0.10 M Na₂SO₄ solution is approximately:
For the sparingly soluble salt Ag₂CrO₄ (K_sp = 1.12 × 10⁻¹²), the correct expression for K_sp in terms of molar solubility *s* is:
Which of the following statements about the common ion effect is correct?
CaF₂ has K_sp = 3.9 × 10⁻¹¹. What is the molar solubility of CaF₂ in a solution that already contains 0.010 M NaF?
If the molar solubility of Mg(OH)₂ in pure water is *s*, the correct K_sp expression is:
The K_sp of PbI₂ is 8.0 × 10⁻⁹. When PbI₂ is dissolved in 0.10 M KI solution, the solubility of PbI₂ is approximately:
Pattern: Compute solubility from K_sp with the common ion effect (PYQ pattern NEET pattern: solubility ksp, observed in NEET 2021 and 2023).
Given
- K_sp(CaF₂) = 3.9 × 10⁻¹¹ - NaF concentration = 0.050 mol/L (part b)
Required
- Molar solubility *s* of CaF₂ in pure water - Molar solubility *s'* of CaF₂ in 0.050 M NaF
Concept
CaF₂ is a sparingly soluble 1:2 salt. Its dissolution equilibrium is CaF₂(s) ⇌ Ca²⁺(aq) + 2F⁻(aq). The K_sp expression must reflect the stoichiometric coefficients as powers. When NaF is added, it supplies F⁻ (the common ion), shifting the equilibrium left and reducing CaF₂ solubility.
Formula
K_sp = [Ca²⁺] · [F⁻]² In pure water: K_sp = s · (2s)² = 4s³ In 0.050 M NaF: K_sp = s' · (2s' + 0.050)²
Substitution
**(a) Pure water:** 4s³ = 3.9 × 10⁻¹¹ s³ = 9.75 × 10⁻¹² **(b) In 0.050 M NaF:** Since s' will be very small (common ion suppresses it), 2s' << 0.050, so [F⁻] ≈ 0.050 M. s' × (0.050)² = 3.9 × 10⁻¹¹ s' × 2.5 × 10⁻³ = 3.9 × 10⁻¹¹
Calculation
**(a)** s = (9.75 × 10⁻¹²)^(1/3) Taking the cube root: 9.75 × 10⁻¹² = 9.75 × 10⁻¹². Cube root of 9.75 ≈ 2.14. Cube root of 10⁻¹² = 10⁻⁴. s ≈ 2.1 × 10⁻⁴ mol/L **(b)** s' = 3.9 × 10⁻¹¹ / 2.5 × 10⁻³ = 1.56 × 10⁻⁸ mol/L **Exact constants note:** The stoichiometric coefficient 2 in "(2s)" and the factor 4 in "4s³" are exact counting numbers and do not limit significant figures.
Final answer
- **(a)** Molar solubility in pure water: s ≈ 2.1 × 10⁻⁴ mol/L - **(b)** Molar solubility in 0.050 M NaF: s' ≈ 1.6 × 10⁻⁸ mol/L The common ion effect reduces CaF₂ solubility by roughly four orders of magnitude — from ~10⁻⁴ to ~10⁻⁸ mol/L.
Common trap
The high-frequency trap here is writing K_sp = s · (2s) = 2s² instead of s · (2s)² = 4s³. This stoichiometric power error gives the wrong solubility in pure water AND the wrong answer in the common ion calculation, because the F⁻ term must be squared. A second common error is forgetting to replace [F⁻] with the external NaF concentration in part (b), effectively solving for pure-water solubility again.
Similar NEET-style question
"The K_sp of Mg(OH)₂ is 5.6 × 10⁻¹². Calculate its molar solubility in 0.10 M NaOH." (Same pattern: 1:2 salt, common ion is OH⁻. Answer: s = K_sp / (0.10)² = 5.6 × 10⁻¹⁰ mol/L.) ---
Suppression of ionisation of a weak electrolyte by adding a strong electrolyte with a common ion. Example: adding NaCl to NH₄OH suppresses NH₄⁺.
-- NCERT Class 11 Chemistry, Ch. 6, p. 32pH 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
Test yourself on this topic with real past-paper questions:
Practice this topic →Get a structured 30-day study plan and a complete formula booklet — delivered to your inbox instantly.