A Level · Chemistry 9701 · Physical chemistry

Acid–base & solubility equilibria: A Level Chemistry questions with answers

Free Acid–base & solubility equilibria questions for A Level Chemistry (9701), part of Physical chemistry. Each question has the answer and the marking points an examiner would look for.

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Acid–base & solubility equilibria practice questions

Question 1Structured · 11 marksA* challenge

A weak acid HA has Ka = 1.74 × 10−5 mol dm−3.

(a)

Calculate the pH of a 0.200 mol dm−3 solution of HA. State one assumption.

[3]
(b)

A buffer contains 0.03 mol HA and 0.015 mol NaA in 1.00 dm3. Calculate its pH, and explain how it resists a change in pH when a small amount of acid is added.

[5]
(c)

A sparingly soluble salt MX has Ksp = 1.8 × 10−10 mol2 dm−6. Calculate its solubility in water and in 0.10 mol dm−3 NaX.

[3]
Show answers and mark scheme
PartAnswer and marking pointsMarks
(a)2.73; [H+] = [A−] and dissociation is negligible
[H+] = √(Kac) C1
2.73 A1
assumption stated B1
3
(b)4.46; A− + H+ → HA, large reservoir of A−
[H+] = Ka[HA]/[A−] C1
4.46 A1
added H+ removed by A− B1
equation A− + H+ → HA B1
ratio [HA]/[A−] changes little B1
5
(c)1.34 × 10−5, 1.80 × 10−9
s = √Ksp C1
1.34 × 10−5 A1
common ion: s = Ksp ÷ 0.10 = 1.80 × 10−9 A1
3
Question 2Structured · 3 marksA* challenge

Solubility product applies to sparingly soluble salts.

(a)

Write the Ksp expression for calcium fluoride, CaF₂.

[1]
(b)

Explain the common ion effect when sodium fluoride is added to a saturated CaF₂ solution.

[2]
Show answers and mark scheme
PartAnswer and marking pointsMarks
(a)Ksp = [Ca²⁺][F⁻]²
Ksp = [Ca²⁺][F⁻]2 B1
1
(b)equilibrium shifts left; precipitate
[F⁻] increases B1
equilibrium shifts to form more CaF₂ precipitate B1
2
Question 3Structured · 9 marks

The solubility product of CaF₂ is 3.90 × 10−11 mol3 dm−9 at 298 K.

(a)

Write the expression for Ksp of this salt.

[1]
(b)

Calculate the solubility of the salt in mol dm−3.

[3]
(c)

Explain the common ion effect and predict how solubility changes in a solution already containing the anion at 0.10 mol dm−3.

[3]
(d)

State whether a precipitate forms when equal volumes of solutions containing 2.0 × 10−3 mol dm−3 of each ion are mixed. Explain.

[2]
Show answers and mark scheme
PartAnswer and marking pointsMarks
(a)[Ca²⁺][F⁻]²
Ksp = [Ca²⁺][F⁻]2 B1
1
(b)2.14 × 10−4 mol dm−3
Ksp = 4s3 M1
s = (Ksp/4)1/3 M1
2.14 × 10−4 mol dm−3 A1
3
(c)added common ion shifts equilibrium to solid; solubility much lower
the equilibrium salt(s) ⇌ ions shifts towards the solid when one of its ions is already present B1
solubility decreases greatly B1
Ksp unchanged B1
3
(d)compare ionic product after dilution with Ksp
concentrations halve on mixing B1
ionic product calculated and compared with Ksp: precipitate if ionic product exceeds Ksp B1
2
Question 4Structured · 3 marks

Calculate the pH of a 0.39 mol dm−3 solution of a weak monoprotic acid with Ka = 1.7 × 10−5 mol dm−3.

[3]
Show answers and mark scheme
PartAnswer and marking pointsMarks
2.59
[H+] = √(Kac) C1
pH = −lg[H+] C1
2.59 A1
3
Question 5Structured · 6 marks

Ethanoic acid has Ka = 1.74 × 10−5 mol dm−3.

(a)

Calculate the pH of a 0.100 mol dm−3 solution of ethanoic acid.

[3]
(b)

Explain how a buffer of ethanoic acid and sodium ethanoate resists a change in pH when acid is added.

[3]
Show answers and mark scheme
PartAnswer and marking pointsMarks
(a)2.88
[H⁺] = √(Kac) C1
[H⁺] = 1.32 × 10−3 C1
pH = 2.88 A1
3
(b)CH₃COO⁻ + H⁺ → CH₃COOH
added H⁺ reacts with ethanoate ions B1
CH₃COO⁻ + H⁺ → CH₃COOH B1
large reservoir of ethanoate, so [H⁺] changes little B1
3
Question 6Structured · 11 marks

1.00 mol of dinitrogen tetroxide is allowed to reach equilibrium at a total pressure of 150 kPa: N₂O₄(g) ⇌ 2NO₂(g), ΔH = +57 kJ mol⁻¹. At equilibrium, 25% of the N₂O₄ has dissociated.

(a)

Write the expression for Kp for this equilibrium.

[1]
(b)

Calculate the mole fraction of each gas at equilibrium.

[2]
(c)

Use your answers to (b) to calculate Kp, giving its units.

[3]
(d)

State and explain the effect on the position of equilibrium of increasing the total pressure at constant temperature.

[2]
(e)

State and explain the effect on the value of Kp of increasing the temperature.

[2]
(f)

Suggest why the colour of the mixture becomes darker when it is heated at constant volume.

[1]
Show answers and mark scheme
PartAnswer and marking pointsMarks
(a)Kp = p(NO₂)²/p(N₂O₄)
Kp = pNO₂2 ÷ pN₂O₄ B1
1
(b)N₂O₄ 0.600; NO₂ 0.400
amounts 0.75 mol N₂O₄ and 0.50 mol NO₂, total 1.25 mol C1
x(N₂O₄) = 0.600, x(NO₂) = 0.400 A1
2
(c)40.0 kPa
partial pressures 90.0 kPa and 60.0 kPa C1
Kp = 60.02 ÷ 90.0 C1
40.0 kPa A1
3
(d)shifts left; fewer gas molecules
shifts to the left B1
fewer moles of gas on the left, which reduces the pressure B1
2
(e)Kp increases; endothermic forward
Kp increases B1
the forward reaction is endothermic, so equilibrium shifts right / to absorb heat B1
2
(f)more brown NO₂
more brown NO₂ forms as the endothermic forward reaction is favoured B1
1

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