NVAEasyJEE 2026Ionic Equilibria & pH

JEE Chemistry 2026 Question with Solution

Consider the dissociation equilibrium of the following weak acid: HAH+(aq)+A(aq)\mathrm{HA \rightleftharpoons H^+(aq) + A^-(aq)} If the pKapK_a of the acid is 44, then the pH of a 10 mM10\ \text{mM} HA solution is _____ (Nearest integer). (Given: The degree of dissociation can be neglected with respect to unity)

Answer

Correct answer:3

Step-by-step solution

Standard Method

Given: Weak acid equilibrium HAH+(aq)+A(aq)\mathrm{HA \rightleftharpoons H^+(aq) + A^-(aq)}, pKa=4pK_a = 4, and initial concentration [HA]0=10 mM=0.01 M[\mathrm{HA}]_0 = 10\ \text{mM} = 0.01\ \text{M}.

Find: The pH of the solution.

Use the acid dissociation relation:

Ka=[H+][A][HA]K_a = \frac{[\mathrm{H^+}][\mathrm{A^-}]}{[\mathrm{HA}]}

From pKa=4pK_a = 4,

Ka=10pKa=104K_a = 10^{-pK_a} = 10^{-4}

Since the degree of dissociation is negligible with respect to unity, take [HA][HA]0=0.01 M[\mathrm{HA}] \approx [\mathrm{HA}]_0 = 0.01\ \text{M} and [H+]=[A]=x[\mathrm{H^+}] = [\mathrm{A^-}] = x. Then,

Ka=x20.01K_a = \frac{x^2}{0.01}

So,

x=Ka×0.01=104×102=106=103 Mx = \sqrt{K_a \times 0.01} = \sqrt{10^{-4} \times 10^{-2}} = \sqrt{10^{-6}} = 10^{-3}\ \text{M}

Thus,

pH=log10[H+]=log10(103)=3\text{pH} = -\log_{10}[\mathrm{H^+}] = -\log_{10}(10^{-3}) = 3

Therefore, the pH of the solution is 33.

Weak Acid Formula

Given: pKa=4pK_a = 4 and concentration C=0.01 MC = 0.01\ \text{M}.

Find: pH.

For a weak acid with small dissociation,

[H+]=KaC[\mathrm{H^+}] = \sqrt{K_a C}

Here Ka=104K_a = 10^{-4} and C=102C = 10^{-2}, so

[H+]=104×102=106=103[\mathrm{H^+}] = \sqrt{10^{-4} \times 10^{-2}} = \sqrt{10^{-6}} = 10^{-3}

Hence,

pH=3\text{pH} = 3

This shortcut works because the weak acid approximation gives [HA]C[\mathrm{HA}] \approx C. The correct answer is 33.

Common mistakes

  • Using 10 mM10\ \text{mM} as 10 M10\ \text{M} is incorrect because milli means 10310^{-3}. Convert properly: 10 mM=0.01 M10\ \text{mM} = 0.01\ \text{M} before applying the weak acid formula.

  • Confusing pKapK_a with pH is incorrect because pKapK_a describes acid strength, not the hydrogen ion concentration of this particular solution. First find KaK_a from pKapK_a, then calculate [H+][\mathrm{H^+}] and pH.

  • Applying the strong acid assumption [H+]=0.01 M[\mathrm{H^+}] = 0.01\ \text{M} is wrong because HA is a weak acid. Use Ka=[H+]2[HA]0K_a = \frac{[\mathrm{H^+}]^2}{[\mathrm{HA}]_0} under the small dissociation approximation instead.

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