AQA A-Level Chemistry Paper 3, June 2025: Question 1
9 marks · Medium difficulty · State/Explain/Numerical
Determine the enthalpy of solution of potassium hydroxide experimentally and theoretically using calorimetry calculations and Born–Haber cycle data.
Practise this questionQuestion
Question text
01 A value for enthalpy of solution can be determined from the results of a calorimetry
experiment or by the application of Hess’s law.
01.1 Give the equation, including state symbols, for the process that occurs when the
enthalpy of solution of potassium hydroxide is determined.
[1 mark]
01.2 A student does an experiment to determine a value for the enthalpy of solution of
potassium hydroxide.
The student uses this method.
• Add some distilled water to a measuring cylinder and record the volume.
• Pour the water into a polystyrene cup.
• Record the temperature of the water in the cup.
• Add 3.00 g of solid KOH to the water in the cup.
• Stir the solution and record the maximum temperature reached.
Table 1 shows the student’s results.
Table 1
Initial temperature / °C 18.1
Final temperature / °C 30.4
The student calculated the enthalpy of solution of potassium hydroxide
to be –51.3 kJ mol–1
The specific heat capacity of the solution, c = 4.18 J K–1 g–1
Assume the density of the solution = 1.00 g cm–3
Calculate the volume of water that the student added to the cup.
[5 marks]
Volume of water 4 Units
01.3 Table 2 shows some enthalpy change data.
Table 2
Enthalpy change / kJ mol–1
Enthalpy of lattice formation of
–789
potassium hydroxide
Enthalpy of hydration of potassium ions –322
Enthalpy of hydration of hydroxide ions –528
Use the data in Table 2 to calculate the enthalpy of solution for potassium hydroxide.
[2 marks]
Enthalpy of solution kJ mol–1
01.4 Suggest why the value calculated in Question 01.3 is different from the
experimental value given in Question 01.2.
[1 mark]
Mark scheme
Show the mark scheme
Question Answers Additional comments/Guidelines Mark
KOH(s) → K+(aq) + OH–(aq) ALLOW (+)aq on arrow
OR ALLOW KOH(aq) as product 1
01.1 KOH(s) + aq → K+(aq) + OH–(aq) IGNORE H O on arrow
State symbols are essential NOT equations with H2O on the LHS and/or RHS (1 x AO1)
NOT ⇌
3.00
M1 Amount of KOH = 56.1 (= 0.053475935 mol)
M2 q = ΔH × 0.0535 ( = 2.74455 kJ) = 2745 J
M2 q = ΔH x M1
For M2, M1 must be an attempt at calculating
amount of KOH
M3 ΔT = 30.4 – 18.1 (= 12.3 °C)
M4/M5 ALLOW actual answers OR actual
𝑞 M2 in J answers minus 3 if mass KOH subtracted
M4 m (= ) = = 49.8 – 50.4 g
c∆T 4.18 × M3
𝑞 M2 in kJ
M4 ALLOW m (= ) = 5
c∆T 4180 × M3
01.2 M4 ALLOW if M2 left in kJ if M5 in dm3
(4 x AO2,
1 x AO3)
52.8 – 53.4 cm3 = 5 marks
Answer must be to min 2 sig. fig. and units of
cm3
ALLOW units of dm3 only if answer given as
M5 = answer to M4 in cm3
0.0528 - 0.0534 dm3 to min 2 sf
M5 2.30 cm3 from ΔT = 12.3 + 273 (NOT M3)
M5 0.998 cm3 comes from 51.3 / 4.18 x 12.3 = M3 &
M5 (NOT M2 & M4). Look for M1 separately
M5 998 cm3 comes from 51300 / 4.18 x 12.3 = M3,
M4 & M5 (NOT M2). Look for M1 separately–A-LEVEL CHEMISTRY– 7405/3 –
Question Answers Additional comments/Guidelines Mark 11
M1 Enthalpy of solution = enthalpy of hydration K+ + enthalpy of OR cycle KOH(s) → K+(aq) + OH–(aq)
hydration OH– – Lattice enthalpy of formation
–789 –322 –528
OR
= –322 – 528 – (–789) K+(g) + OH–(g)
OR 2
01.3 –789 + x = –322 + (–528)
–61 = 2 marks (2 x AO2)
M2 –61 (kJ mol–1)
+61 = 1 mark
–1639 = 1 mark
NOT +1639 (0 marks)
ALLOW incomplete dissociation/reaction
ALLOW solution made in experiment is not to
infinite dilution
ALLOW thermal energy for ‘heat’
IGNORE not standard conditions / covalent
character / evaporation of water / apparatus
uncertainty 1
01.4 Heat losses OR incomplete dissolving IGNORE energy loss unqualified
(1 x AO3)
IGNORE human error
IGNORE incomplete hydration
NOT data book values are averages
NOT incomplete combustion
NOT heat gain
NOT references to yield
How to answer it
Enthalpy of Solution & Calorimetry Analysis
This question assesses your mastery of enthalpy of solution across both experimental and theoretical thermochemistry. You are tested on:
- Writing precise dissolution equations with compulsory state symbols.
- Carrying out a reverse calorimetry calculation using q = mcΔT and ΔH = −q / n to find the unknown volume of water.
- Applying Hess's Law using lattice enthalpy of formation and hydration enthalpies.
- Evaluating experimental errors that cause experimental values to deviate from theoretical values.
Dissolution Equation for KOH
Writing the process for enthalpy of solution
✅ Correct Answer
KOH(s) → K⁺(aq) + OH⁻(aq)
Also allowed: KOH(s) + aq → K⁺(aq) + OH⁻(aq) or KOH(s) → KOH(aq)
💡 Key Knowledge
Enthalpy of solution is the enthalpy change when 1 mole of an ionic solid dissolves completely in water to give infinitely dilute aqueous ions.
- LHS must be 1 mole of solid: KOH(s).
- RHS must be separated aqueous ions: K⁺(aq) and OH⁻(aq).
❌ Common Errors
- Writing H₂O on the LHS as a reactant (e.g. KOH + H₂O → ... ) — 0 marks. H₂O acts as the solvent, not a stoichiometric reactant.
- Using a reversible arrow (⇌) instead of an irreversible arrow (→) — 0 marks.
- Omitting state symbols — the question explicitly states: "including state symbols".
🧠 Exam Technique
Always inspect the wording: if it asks for "enthalpy of solution", start from the solid ionic lattice and finish with hydrated ions.
Reverse Calorimetry Calculation
Calculating the volume of water from temperature rise and enthalpy
📐 Step-by-Step Calculation
- Find the moles of KOH:
Mr(KOH) = 39.1 + 16.0 + 1.0 = 56.1 g mol⁻¹
n(KOH) = 3.00 / 56.1 = 0.05348 mol (M1) - Calculate heat released (q):
ΔH = −51.3 kJ mol⁻¹, so heat evolved is exothermic:
q = n × |ΔH| = 0.05348 mol × 51.3 kJ mol⁻¹ = 2.743 kJ = 2743 J (or 2745 J) (M2) - Find the temperature change (ΔT):
ΔT = 30.4 − 18.1 = 12.3 °C (or 12.3 K) (M3) - Rearrange q = mcΔT to find mass of water (m):
m = q / (c × ΔT) = 2743 / (4.18 × 12.3) = 53.4 g (M4) - Convert mass to volume with units:
Since density = 1.00 g cm⁻³: Volume = 53.4 cm³ (allow range 52.8 to 53.4 cm³) (M5)
Note: If mass of KOH (3.00 g) is subtracted from total mass, volume = 50.4 cm³ (range 49.8 – 50.4 cm³) is fully allowed.
✅ Final Answer
Volume of water = 53.4 (or 53)
Units = cm³ (or 0.0534 dm³)
❌ Common Calculation Traps
- Unit clash in q: Substituting ΔH in kJ directly into q = mcΔT where c is in J K⁻¹ g⁻¹. You must multiply kJ by 1000 to get J!
- Missing unit on the dotted line: Students often leave the separate "Units" line blank, forfeiting M5.
- Temperature in Kelvin: Attempting to convert 12.3 °C by adding 273. The difference ΔT is 12.3 whether in °C or K!
Enthalpy of Solution via Hess's Cycle
Using Born-Haber / Lattice & Hydration Data
📐 Calculation & Cycle
By Hess's Law:
ΔHsoln = ΣΔHhyd − ΔHlatt formation
or:
ΔHsoln = ΔHlatt dissociation + ΣΔHhyd
Substituting values:
ΔHsoln = (−322) + (−528) − (−789)
ΔHsoln = −850 + 789 = −61 kJ mol⁻¹
💡 Visualising the Hess Cycle
Consider the two routes from KOH(s) to K⁺(aq) + OH⁻(aq):
- Direct route: ΔHsoln
- Indirect route:
1. Break lattice into gaseous ions: −ΔHlatt form = −(−789) = +789 kJ mol⁻¹
2. Hydrate gaseous ions: ΔHhyd(K⁺) + ΔHhyd(OH⁻) = (−322) + (−528) = −850 kJ mol⁻¹
Direct = Indirect: +789 + (−850) = −61 kJ mol⁻¹
✅ Correct Answer
Enthalpy of solution = −61 kJ mol⁻¹
❌ Common Sign Traps
- Confusing formation vs. dissociation: The table gives lattice formation (−789). Dissociating the solid into ions requires +789 kJ mol⁻¹.
- Writing +61 (gives 1/2 marks) — sign error.
- Writing −1639 (gives 1/2 marks) — added all three numbers directly without reversing lattice formation.
Evaluating Experimental Discrepancies
Explaining differences between theoretical and experimental results
✅ Accepted Answers
- Heat losses (or thermal energy lost to surroundings/cup).
- Incomplete dissolving of the KOH solid.
- Also allowed: Incomplete dissociation; solution was not at infinite dilution.
🧠 Why does this explain the difference?
The calculated theoretical value was −61 kJ mol⁻¹, whereas the experimental value was only −51.3 kJ mol⁻¹ (less exothermic).
If heat is lost to the surroundings or if some solid remains undissolved, the observed temperature rise will be lower than expected, resulting in a less negative calculated experimental enthalpy.
❌ Rejected Responses (Do NOT write these!)
- "Data book values are averages" — 0 marks. Lattice and hydration enthalpies are specific to these exact ions, NOT mean values like bond enthalpies!
- "Human error" or "Energy loss" unqualified — 0 marks. Must specify heat or thermal energy lost.
- "Incomplete combustion" — 0 marks. This is a dissolution experiment, not a combustion reaction!
- "Covalent character" — 0 marks. Lattice formation was given directly, not calculated via pure ionic Kapustinskii/Born-Landé models.
Topics
Physical Chemistry · Required Practicals · 3.1.4 Energetics · 3.1.8 Thermodynamics · Required Practical 2: Measurement of an enthalpy change
Question and mark scheme from the AQA A-Level Chemistry examination, Paper 3, June 2025. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.