AQA A-Level Chemistry Paper 1, June 2024: Question 7
8 marks · Medium difficulty · State/Explain/Numerical
Write the expression for Kw, calculate the pH of pure water at 40 °C, and calculate the pH of a mixture of aqueous sodium hydroxide and hydrochloric acid at 40 °C.
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Question text
07 At 40 °C the ionic product of water, K = 2.92 × 10–14 mol2 dm–6
w
07.1 Give the expression for Kw
Calculate the pH of pure water at 40 °C
Give your answer to 2 decimal places.
[3 marks]
Kw
pH
07.2 35.0 cm3 of 0.150 mol dm–3 aqueous sodium hydroxide are mixed with
20.0 cm3 of a 0.100 mol dm–3 solution of hydrochloric acid.
The temperature of the solution formed is 40 °C
Calculate the pH of the solution formed.
Give your answer to 2 decimal places.
[5 marks]
pH
Mark scheme
Show the mark scheme
Question Answers Additional comments/Guidelines Mark
M1 K = [H+] [OH–]
w
07.1 M2 [H+] = √2.92 × 10–14
(1 × AO1,
2 × AO2)
M3 = –log10 M2
M3 pH = 6.77
answer to 2 decimal places
M1 n OH– = 5.25 × 10–3 and n H+ = 2.00 × 10–3 mol
– –3 M2 = n(OH–) – n(H+) in M1
M2 excess OH = 3.25 × 10 mol
–3 𝑀𝑀2
– 3.25×10 –3 M3 =
M3 [OH ] = = 0.0591 mol dm 55 𝑥𝑥 10−3
55.0×10–3
07.2
(5 x AO2)
2.92 𝑥𝑥 10−14
2.92×10–14 M4 =
M4 [H+] = = 4.94 × 10–13 mol dm–3
𝑀𝑀3
0.0591
M5 12.31 M5 = –log10(M4)
How to answer it
Water Dissociation & Acid-Base Mixture pH
This question assesses quantitative acid-base equilibrium concepts from Physical Chemistry:
- Writing the equilibrium expression for the ionic product of water ( Kw ).
- Calculating the pH of pure water at non-standard temperatures (where pH ≠ 7.00 ).
- Carrying out multi-step stoichiometric calculations for the reaction between a strong monoprotic acid and a strong monoacidic base.
- Calculating excess hydroxide concentration using the total combined solution volume.
- Using Kw at a stated temperature to calculate [H⁺] and converting to pH rounded to 2 decimal places.
Expression for Kw & pH of Pure Water at 40 °C
Definition of Kw and neutral water calculation
💡 Key Knowledge
- Auto-ionisation of water:
H₂O(l) ⇌ H⁺(aq) + OH⁻(aq) (endothermic). - Because water is a liquid in huge excess, [H₂O] is effectively constant and incorporated into Kw :
Kw = [H⁺][OH⁻] - In pure water, every molecule that ionises produces equal concentrations of H⁺ and OH⁻:
[H⁺] = [OH⁻] , therefore Kw = [H⁺]² . - Water at 40 °C is still strictly neutral despite having a pH < 7 because [H⁺] equals [OH⁻].
📐 Step-by-Step Calculation
- 1 State expression:
Kw = [H⁺][OH⁻] [Mark 1] - 2 Find [H⁺]:
Since [H⁺] = [OH⁻]:
[H⁺] = √(Kw) = √(2.92 × 10⁻¹⁴)
[H⁺] = 1.7088 × 10⁻⁷ mol dm⁻³ [Mark 2] - 3 Calculate pH:
pH = -log₁₀[H⁺]
pH = -log₁₀(1.7088 × 10⁻⁷) = 6.767...
pH = 6.77 (2 d.p.) [Mark 3]
✅ Final Credited Answers
- Kw expression: Kw = [H⁺][OH⁻] (square brackets are mandatory to denote concentration)
- pH: 6.77
❌ Common Errors & Traps
- Including [H₂O]: Writing Kw = [H⁺][OH⁻]/[H₂O] is an equilibrium constant (Kc), not Kw. Scores zero.
- Assuming pH = 7: Remembering standard room temperature pH and not calculating based on the given Kw value.
- Rounding too early: Rounding [H⁺] to 1.7 × 10⁻⁷ gives pH = 6.769 = 6.77 (safe here, but early rounding frequently costs marks).
- Wrong decimal places: Giving 6.8 or 6.767 instead of the required 2 decimal places.
pH of a Strong Acid – Strong Base Mixture
Mixing 35.0 cm³ of 0.150 mol dm⁻³ NaOH with 20.0 cm³ of 0.100 mol dm⁻³ HCl at 40 °C
📐 Complete 5-Step Calculation Plan
- 1 Calculate initial moles of H⁺ and OH⁻:
Both HCl and NaOH are strong and monoprotic (100% dissociated).
• Moles of OH⁻ = (35.0 / 1000) × 0.150 = 5.25 × 10⁻³ mol
• Moles of H⁺ = (20.0 / 1000) × 0.100 = 2.00 × 10⁻³ molAward M1 for calculating both mole values correctly. - 2 Determine which reagent is in excess:
Reaction: H⁺(aq) + OH⁻(aq) → H₂O(l) (1:1 stoichiometric ratio).
OH⁻ is in excess since 5.25 × 10⁻³ > 2.00 × 10⁻³.
• Excess moles of OH⁻ = 5.25 × 10⁻³ - 2.00 × 10⁻³ = 3.25 × 10⁻³ molAward M2 for subtracting moles of acid from moles of alkali. - 3 Calculate concentration of excess OH⁻ using TOTAL volume:
• Total volume = 35.0 + 20.0 = 55.0 cm³ = 55.0 × 10⁻³ dm³
• [OH⁻] = (3.25 × 10⁻³) / (55.0 × 10⁻³) = 0.05909... mol dm⁻³ (or 0.0591 mol dm⁻³)Award M3 for dividing excess moles by total volume (in dm³). - 4 Calculate [H⁺] using Kw at 40 °C:
Rearrange Kw = [H⁺][OH⁻] to give [H⁺] = Kw / [OH⁻]
• [H⁺] = (2.92 × 10⁻¹⁴) / 0.05909... = 4.9416 × 10⁻¹³ mol dm⁻³Award M4 for dividing 2.92 × 10⁻¹⁴ by their [OH⁻]. - 5 Calculate final pH:
• pH = -log₁₀[H⁺] = -log₁₀(4.9416 × 10⁻¹³) = 12.306...
• pH = 12.31 (to 2 d.p.)Award M5 for final pH = 12.31 (strictly to 2 decimal places).
🧠 Exam Technique & Alternative Method
Alternative via pOH:
- Calculate pKw = -log₁₀(2.92 × 10⁻¹⁴) = 13.535
- Calculate pOH = -log₁₀(0.05909) = 1.228
- pH = pKw - pOH = 13.535 - 1.228 = 12.31
- Warning: Do NOT subtract from 14.00! pH + pOH = 14 only applies at 25 °C. At 40 °C, pH + pOH = 13.54 .
❌ Major Examiner Traps
- Forgetting total volume (The #1 Error): Dividing excess moles by 35.0 cm³ instead of (35.0 + 20.0 = 55.0 cm³). This loses M3, M4, and M5.
- Using standard Kw (1.00 × 10⁻¹⁴): Failing to use the value provided at 40 °C ( 2.92 × 10⁻¹⁴ ). Doing this loses M4 and M5.
- Decimal Places: pH values should always be quoted to 2 decimal places in AQA exams unless stated otherwise. Writing 12.3 or 12 loses the final mark.
Topics
Physical Chemistry · 3.1.12 Acids and Bases · 3.1.2 Amount of Substance
Question and mark scheme from the AQA A-Level Chemistry examination, Paper 1, June 2024. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.