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Polyprotic acids

Chemistry • Acid–Base Equilibria • Knowledge-Based • 5 questions

Polyprotic acids Knowledge-Based Download PDF

Chemistry · Acids & Bases · Chemistry · Acid–Base Equilibria

5 Chemistry practice questions on Polyprotic acids. Questions that assess core concepts and understanding.

Questions

  1. 1.

    For an aqueous solution containing the divalent anion A2−\text{A}^{2-} derived from a weak diprotic acid H2A\text{H}_2\text{A}, which expression correctly defines the first base dissociation constant, Kb1K_{b1}, in terms of the ion-product constant of water, KwK_w, and the stepwise acid dissociation constants of H2A\text{H}_2\text{A}?

    • A) Kb1=KwKa1K_{b1} = \frac{K_w}{K_{a1}}
    • B) Kb1=KwKa2K_{b1} = \frac{K_w}{K_{a2}}
    • C) Kb1=KwKa1Ka2K_{b1} = \frac{K_w}{K_{a1} K_{a2}}
    • D) Kb1=Ka2KwK_{b1} = \frac{K_{a2}}{K_w}
  2. 2.

    Which expression gives the approximate hydronium ion concentration, [H3O+][H_3O^+], in an aqueous solution of the intermediate amphiprotic salt NaHANaHA derived from a weak diprotic acid, H2AH_2A, assuming the analytical salt concentration CC is sufficiently high and water autoionization is negligible?

    • A) [H3O+]≈Ka1C[H_3O^+] \approx \sqrt{K_{a1} C}
    • B) [H3O+]≈Ka1+Ka22[H_3O^+] \approx \frac{K_{a1} + K_{a2}}{2}
    • C) [H3O+]≈Ka1Ka2[H_3O^+] \approx \sqrt{K_{a1} K_{a2}}
    • D) [H3O+]≈Ka2C[H_3O^+] \approx \sqrt{K_{a2} C}
  3. 3.

    Why is the second acid dissociation constant (Ka2K_{a2}) of a weak polyprotic acid typically several orders of magnitude smaller than its first acid dissociation constant (Ka1K_{a1})?

    • A) The second ionization step generates hydroxide ions that inhibit further proton loss through the common-ion effect.
    • B) Electrostatic attraction makes removing a positively charged proton from a negatively charged anion significantly more difficult than from a neutral molecule.
    • C) The conjugate base produced in the first ionization step is insoluble in water, preventing further dissociation.
    • D) The activation energy for the first proton transfer is substantially higher than the activation energy of the second step.
  4. 4.

    For a 0.10 M aqueous solution of a weak triprotic acid, H3A\text{H}_3\text{A}, with successive dissociation constants Ka1=1.0×10−3K_{a1} = 1.0 \times 10^{-3}, Ka2=1.0×10−7K_{a2} = 1.0 \times 10^{-7}, and Ka3=1.0×10−12K_{a3} = 1.0 \times 10^{-12}, which of the following lists the acid-derived species in order of decreasing equilibrium concentration?

    • A) [A3−]>[HA2−]>[H2A−]>[H3A][\text{A}^{3-}] > [\text{HA}^{2-}] > [\text{H}_2\text{A}^-] > [\text{H}_3\text{A}]
    • B) [H2A−]>[HA2−]>[A3−]>[H3A][\text{H}_2\text{A}^-] > [\text{HA}^{2-}] > [\text{A}^{3-}] > [\text{H}_3\text{A}]
    • C) [H3A]>[H2A−]>[HA2−]>[A3−][\text{H}_3\text{A}] > [\text{H}_2\text{A}^-] > [\text{HA}^{2-}] > [\text{A}^{3-}]
    • D) [H3A]>[HA2−]>[H2A−]>[A3−][\text{H}_3\text{A}] > [\text{HA}^{2-}] > [\text{H}_2\text{A}^-] > [\text{A}^{3-}]
  5. 5.

    For an aqueous solution of a weak diprotic acid, H2AH_2A, with successive ionization constants Ka1K_{a1} and Ka2K_{a2} such that Ka1≫Ka2K_{a1} \gg K_{a2}, which expression correctly approximates the equilibrium concentration of the divalent anion, [A2−][A^{2-}]?

    • A) [A2−]≈Ka1⋅Ka2[A^{2-}] \approx \sqrt{K_{a1} \cdot K_{a2}}
    • B) [A2−]≈Ka2⋅[H2A]0[A^{2-}] \approx \sqrt{K_{a2} \cdot [H_2A]_0}
    • C) [A2−]≈Ka1Ka2[A^{2-}] \approx \frac{K_{a1}}{K_{a2}}
    • D) [A2−]≈Ka2[A^{2-}] \approx K_{a2}