Common Ion Effect

8 MCQs1 revision card9-step worked example
Source: NCERT EquilibriumPYQ coverage: NEET 2021, 2022, 2023, 2024, 2025Official key: NTA-verifiedLast reviewed: May 2026

Lesson

The 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.


Practice MCQs

Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.

MCQ 1Direct ApplicationPractice

The solubility product of PbCl₂ is 1.6 × 10⁻⁵. What is the molar solubility of PbCl₂ in pure water?

MCQ 2Easy RecallPractice

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?

MCQ 3Direct ApplicationPractice

The K_sp of BaSO₄ is 1.1 × 10⁻¹⁰. Its molar solubility in 0.10 M Na₂SO₄ solution is approximately:

MCQ 4Direct ApplicationPractice

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:

MCQ 5Easy RecallPractice

Which of the following statements about the common ion effect is correct?

MCQ 6CalculationPractice

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?

MCQ 7Easy RecallPractice

If the molar solubility of Mg(OH)₂ in pure water is *s*, the correct K_sp expression is:

MCQ 8CalculationPractice

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:

Quick recall before you leave

Worked Example

Pattern: Compute solubility from K_sp with the common ion effect (PYQ pattern NEET pattern: solubility ksp, observed in NEET 2021 and 2023).

  1. 1

    Given

    - K_sp(CaF₂) = 3.9 × 10⁻¹¹ - NaF concentration = 0.050 mol/L (part b)

  2. 2

    Required

    - Molar solubility *s* of CaF₂ in pure water - Molar solubility *s'* of CaF₂ in 0.050 M NaF

  3. 3

    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.

  4. 4

    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

  5. 5

    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

  6. 6

    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.

  7. 7

    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.

  8. 8

    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.

  9. 9

    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.) ---

Before solving, remember these

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. 32

Formulas

Henderson-Hasselbalch (buffer)

pH of acidic buffer in terms of conjugate base/acid concentrations. For basic buffer: pOH = pKb + log10([salt]/[base]).

SymbolQuantitySI Unit
pKa-log Ka-
[salt]conjugate base concmol/L
[acid]weak acid concmol/L

Valid when

  • Buffer (weak acid + conjugate base)
  • Concentrations not too dilute
  • Approximate (assumes negligible dissociation)

Ka, Kb, Kw relationship

Stronger acid → weaker conjugate base, and vice versa. pKa + pKb = 14.

SymbolQuantitySI Unit
Kaacid dissociation-
Kbbase dissociation-
Kwwater 10^-14-

Valid when

  • Conjugate acid-base pair
  • 25°C

Equilibrium constant K_p and K_c

Convert between pressure-based and concentration-based equilibrium constants. T in K; R = 0.0821 L atm/mol/K (when K_p in atm).

SymbolQuantitySI Unit
K_ppressure constant-
K_cconcentration constant-
Δnmole change-

Valid when

  • Gas-phase equilibrium
  • Same temperature

Solubility product

Equilibrium constant for sparingly soluble salt. Q < K_sp: dissolves; Q > K_sp: precipitates.

SymbolQuantitySI Unit
K_spsolubility product-

Valid when

  • Sparingly soluble salt
  • Saturated solution

pH and pOH

Logarithmic acidity scale. Pure water at 25°C: pH = 7 = pOH.

SymbolQuantitySI Unit
[H+]hydrogen ion concmol/L
[OH-]hydroxide concmol/L

Valid when

  • Aqueous solution
  • Use Kw = 10^-14 at 25°C

Exam Traps & Common Mistakes

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.

When it triggers

Question lists catalyst addition among options for shifting equilibrium.

How to avoid

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.

When it triggers

Convert K_p ↔ K_c for gas-phase reaction.

How to avoid

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.

When it triggers

K_sp problem with non-1:1 salt (e.g. CaF₂, Mg(OH)₂, Ag₂CrO₄).

How to avoid

Write dissolution: M_aX_b → aM + bX. Then K_sp = [M]^a · [X]^b. For CaF₂ ↔ Ca + 2F: K_sp = s · (2s)² = 4s³.

Past Year Questions

15 questions from NEET 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.

NEET 2023

Which complex compound is most stable?

1CoNH  NO    3 3 3 3
2CoCl en NO  2 2 3
3CoNH   SO   3 6 2 4 3
4CoNH  H OBrNO   3 4 2  3 2
NTA Answer: Option 2(final)
NEET 2022

Choose the correct statement:

1Both diamond and graphite are used as dry lubricants.
2Diamond and graphite have two dimensional network.
3Diamond is covalent and graphite is ionic.
4Diamond is sp3 hybridised and graphite is sp2 hybridized.
NTA Answer: Option 4(final)

How NEET usually asks this

Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.

Sources

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