ClO2-(aq) + HCOOH(aq) ⇄ HClO2(aq) + HCOO-(aq) Keq < 1 What are the relative strengths of the acids a — Acids and Bases Chemistry Question
Question
ClO2-(aq) + HCOOH(aq) ⇄ HClO2(aq) + HCOO-(aq) Keq < 1
What are the relative strengths of the acids and bases in the reaction represented by the equation above?
Acid Strength: HClO2 < HCOOH; Base Strength: ClO2- < HCOO-
Acid Strength: HClO2 < HCOOH; Base Strength: ClO2- > HCOO-
Acid Strength: HClO2 > HCOOH; Base Strength: ClO2- > HCOO-
Acid Strength: HClO2 > HCOOH; Base Strength: ClO2- < HCOO-
💡 Solution & Explanation
STEPS:
1. Identify the Brønsted-Lowry acids and bases on both sides of the equation:
* Reactants side: Formic acid, , acts as the proton donor (acid), while the chlorite ion, , acts as the proton acceptor (base).
* Products side: Chlorous acid, , acts as the conjugate acid (capable of donating a proton in the reverse reaction), while the formate ion, , acts as the conjugate base (capable of accepting a proton in the reverse reaction).
2. Interpret the thermodynamic meaning of the equilibrium constant ():
* An equilibrium constant of less than 1 () indicates that the reactants are favored at equilibrium.
* This means that under equilibrium conditions, the concentration of the reactants ( and ) is significantly higher than the concentration of the products ( and ).
3. Apply the fundamental rule of acid-base equilibrium:
* In any Brønsted-Lowry acid-base reaction, proton-transfer equilibria always favor the side of the reaction with the weaker acid and the weaker base.
* This occurs because stronger acids have a greater tendency to lose protons, and stronger bases have a greater tendency to attract protons, reacting highly efficiently to produce their more stable, weaker counterparts.
4. Determine the relative acid strengths:
* Since the reactants are favored at equilibrium, the reactant acid () must be the weaker acid, and the product acid () must be the stronger acid:
5. Determine the relative base strengths:
* Since the reactants are favored at equilibrium, the reactant base () must be the weaker base, and the product conjugate base () must be the stronger base:
* *Note: This perfectly aligns with conjugate acid-base theory, which states that a stronger acid () must conjugate to a weaker base (), and a weaker acid () must conjugate to a stronger base ().*
6. Select the matching option:
* Combining these two relative strengths ( and ) identifies Option D as the correct answer.
*
WHY_OTHERS_WRONG:
- Option A is incorrect: This option claims that is a weaker acid than and that is a weaker base than . This is a conceptual mismatch; it places the weaker acid and the stronger base on opposite sides of the equilibrium, which violates conjugate acid-base rules. Furthermore, if were the stronger acid, the forward reaction would be favored, leading to a .
- Option B is incorrect: This option states that is the stronger acid and is the stronger base. If both reactants were the stronger species, they would react forward almost completely to establish equilibrium, resulting in a product-favored system with a .
- Option C is incorrect: While this option correctly identifies that is the stronger acid, it incorrectly claims that is the stronger base. Because a stronger acid is always coupled with a weaker conjugate base, the stronger acid must have a weaker conjugate base than does, meaning must be a weaker base than .