The first and second ionization constants of H2X are 2.5 × 10⁻8 and 1.0 × 10⁻13 respectively. The concentration of X2− in 0.1 M H2X solution is
Q. The first and second ionization constants of H2X are 2.5 × 10⁻8 and 1.0 × 10⁻13 respectively.

The concentration of X2− in 0.1 M H2X solution is ______ × 10⁻15 M. (Nearest Integer)
Correct Answer: 100

Explanation (Complete Step-by-Step Calculation)

Given:

\[ K_{a1} = 2.5 \times 10^{-8} \]

\[ K_{a2} = 1.0 \times 10^{-13} \]

Initial concentration of H₂X = 0.1 M


Step 1: First dissociation

\[ H_2X \rightleftharpoons H^+ + HX^- \]

Since Ka₁ is small, weak acid approximation applies:

\[ [H^+] \approx \sqrt{K_{a1} \times C} \]

\[ = \sqrt{2.5 \times 10^{-8} \times 0.1} \]

\[ = \sqrt{2.5 \times 10^{-9}} \]

\[ = 5 \times 10^{-5} \text{ M} \]


Step 2: Second dissociation

\[ HX^- \rightleftharpoons H^+ + X^{2-} \]

\[ K_{a2} = \frac{[H^+][X^{2-}]}{[HX^-]} \]

Rearranging:

\[ [X^{2-}] = \frac{K_{a2}[HX^-]}{[H^+]} \]

From first dissociation:

\[ [HX^-] \approx [H^+] = 5 \times 10^{-5} \]

Therefore:

\[ [X^{2-}] = \frac{1.0 \times 10^{-13} \times 5 \times 10^{-5}}{5 \times 10^{-5}} \]

\[ [X^{2-}] = 1.0 \times 10^{-13} \]


But note:

\[ [H^+] = 5 \times 10^{-5} \]

More accurate relation for diprotic acid:

\[ [X^{2-}] = \frac{K_{a1}K_{a2}C}{[H^+]^2} \]

Substitute values:

\[ = \frac{(2.5 \times 10^{-8})(1.0 \times 10^{-13})(0.1)}{(5 \times 10^{-5})^2} \]

\[ = \frac{2.5 \times 10^{-22}}{25 \times 10^{-10}} \]

\[ = 1.0 \times 10^{-13} \]

Express in form ______ × 10⁻15:

\[ 1.0 \times 10^{-13} = 100 \times 10^{-15} \]

Final Answer = 100

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