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Ka, pKa and weak acid pHEdexcel A-Level Chemistry: Subtopic test

10 questions, 27 marks

Edexcel A-Level Chemistry

Ka, pKa and weak acid pH

Total 27 marks

Name

Class

Date

  1. 1
    A food technologist analyses a 0.100 mol dm⁻³ solution of ethanoic acid, CH₃COOH, a weak monobasic acid, at 298 K. For ethanoic acid, KaK_a = 1.74 × 10⁻⁵ mol dm⁻³.
    (a)
    Which expression gives the acid dissociation constant, KaK_a, for ethanoic acid in aqueous solution?
    [1 mark]
    • A[CH3COOH][H+][CH3COO−]\frac{[CH_3COOH]}{[H^+][CH_3COO^-]}
    • B[H+][CH3COO−][H2O][CH3COOH]\frac{[H^+][CH_3COO^-]}{[H_2O][CH_3COOH]}
    • C[H+][CH3COO−][CH3COOH]\frac{[H^+][CH_3COO^-]}{[CH_3COOH]}
    • D[H+][CH3COO−][H^+][CH_3COO^-]
    (b)
    What is the pKₐ of ethanoic acid?
    [1 mark]
    • A4.76
    • B9.24
    • C1.74
    • D−4.76
    (c)
    Calculate the pH of the 0.100 mol dm⁻³ ethanoic acid solution. State the assumptions you make.
    [2 marks]

    Total for question 1: 4 marks

  2. 2
    A chemist prepares a 0.0500 mol dm⁻³ solution of methanoic acid, HCOOH, for use as a descaling agent. For methanoic acid, KaK_a = 1.78 × 10⁻⁴ mol dm⁻³ at 298 K. She compares it with propanoic acid, which has pKₐ = 4.87.
    (a)
    The chemist calculates the pH of the methanoic acid using [H+]=Kac[H^+] = \sqrt{K_a c}. Which pair of assumptions is needed for this expression?
    [1 mark]
    • AThe acid is fully dissociated, and [H+][H^+] equals the initial acid concentration
    • B[H+]=[HCOO−][H^+] = [HCOO^-] (water's ionisation is negligible), and the equilibrium [HCOOH][HCOOH] is approximately its initial concentration
    • CKaK_a is zero, and the solution is at 25 °C
    • D[H+][H^+] is much greater than [HCOO−][HCOO^-], and the equilibrium [HCOOH][HCOOH] is zero
    (b)
    Which statement about the two acids is correct?
    [1 mark]
    • APropanoic acid is the stronger acid because its pKₐ is larger
    • BThe two acids have the same KaK_a because both are weak
    • CPropanoic acid has the larger KaK_a because its pKₐ is larger
    • DMethanoic acid is the stronger acid because its pKₐ (3.75) is lower, corresponding to a larger KaK_a
    (c)
    The chemist states that the pH of the methanoic acid solution is greater than that of a 0.0500 mol dm⁻³ solution of a strong monobasic acid. Explain why.
    [2 marks]

    Total for question 2: 4 marks

  3. 3
    A student dissolves 0.440 g of a pure solid weak monobasic acid, HA (molar mass 88.0 g mol⁻¹), in water and makes the solution up to 100 cm³. A calibrated pH meter reads 3.06 at 298 K.
    (a)
    Calculate KaK_a for the acid HA. State the assumptions you make.
    [3 marks]
    (b)
    A second student finds KaK_a for the same acid by titration with sodium hydroxide and a pH meter. Describe how KaK_a can be found from the results, and explain why the method works.
    [4 marks]

    Total for question 3: 7 marks

  4. 4
    A chemist compares two 0.100 mol dm⁻³ acids at 298 K: ethanoic acid (CH₃COOH, KaK_a = 1.74 × 10⁻⁵ mol dm⁻³) and chloroethanoic acid (CH₂ClCOOH, KaK_a = 1.38 × 10⁻³ mol dm⁻³). Both are weak monobasic acids.
    (a)
    A 25.0 cm³ sample of 0.250 mol dm⁻³ ethanoic acid is diluted to 250 cm³. Calculate the pH of the solution before and after dilution, and explain why the pH does not rise by exactly 1.
    [6 marks]
    (b)
    Evaluate whether KaK_a and pKₐ allow the strengths of the two acids to be compared, and whether the approximation [HA]eq≈[HA]initial[HA]_{eq} \approx [HA]_{initial} is equally valid for both when calculating pH.
    [6 marks]

    Total for question 4: 12 marks

End of questions

Written by the Exaim team, led by Shaun Daswani (Head of Upper Secondary, Improve ME Institute; MSc Financial Mathematics, Imperial College London; BSc, UCL) and Jason Daswani (operational lead, Improve ME Institute; LSE).