Edexcel A-Level Chemistry AS Paper 2, November 2021: Question 9
17 marks · Medium difficulty · Open Response
Calculate the enthalpy change for the formation of ammonia using mean bond enthalpies, determine atom economy, identify Kc expressions, and explain heterogeneous catalysis and equilibrium removal.
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Question text
9 An equation for the formation of ammonia using the Haber process is shown.
N2(g) + 3H2(g) 2NH3(g)
(a) (i) Calculate the enthalpy change for the forward reaction shown in the equation,
selecting from the bond enthalpies in the table.
Include a sign in your answer.
(3)
Bond Mean bond enthalpy / kJ mol–1
N N 158
N N 410
N N 945
N H 391
H H 436
(ii) A data book gives the standard enthalpy change of formation of ammonia
as –46.1 kJ mol–1.
Give two reasons for the difference between this value and the value that you
calculated in (a)(i).
(2)
Reason 1
Reason 2
(iii) What is the percentage atom economy, by mass, for ammonia in the
forward reaction?
N2(g) + 3H2(g) 2NH3(g)
(1)
A 17.6%
B 50.0%
22 C 82.4%
D 100% *P67084A02228*
(iv) What is the equilibrium expression for Kc?
(1)
[N ][3H ]22
A Kc =
[2NH ]3
[2NH ]3
B Kc =
[N ][3H ]22
[NH ]2
C K = 3
c 3
[N ][H ]22
[N ][H ]3
D K = 2 2
c 2
[NH ]3
(b) In the chemical industry, many processes involve reversible reactions. The product
is often removed before equilibrium is attained. 23
Give three reasons why the product may be removed before its maximum*P67084A02328*
concentration is achieved.
(3)
(c) Ammonia is stable in air but can be oxidised on the surface of a copper catalyst.
An equation for this reaction is
4NH (g) + 5O (g) → 6H O(g) + 4NO(g) Δ H = –905.2 kJ mol–1
32 2 r
The catalyst is usually warmed to approximately 300°C to start the reaction, but
after a short reaction time the copper catalyst often melts.
(i) Give a reason why the catalyst is warmed and a reason why the catalyst may melt.
(2)
… 24
… *P67084A02428*
(ii) Complete the reaction profile for this catalysed oxidation of ammonia,
showing the enthalpy change, ΔrH.
(2)
Reactants
Enthalpy
Reaction path
(iii) Describe the processes that occur on the surface of a heterogeneous catalyst
during the oxidation of ammonia in air.
(3)
… *P67084A02528*
… 26
*P67084A02628*(Total for Question 9 = 17 marks)
Mark scheme
Show the mark scheme
Question Answer Additional Guidance
Number Mark
9(a)(i) Example of calculation (3)
• sum of bond energies of all reactants (1) 945 + (3 × 436) = (+)2253 (kJ mol-1)
6(N−H) = 6 × 391 = (−)2346 (kJ mol-1)
• sum of bond energies of all products (1)
−2346 + 2253 = −93 (kJ mol-1)
• calculation of ∆rH (1)
TE from either/both M1 and M2
Correct answer with no working scores 3
Question Answer Additional Guidance Mark
Number
9(a)(ii) An answer that makes reference to the following points: (2)
• the equation in 9(a)(i) is for the formation of two moles of Ignore any references to differing conditions for the
ammonia (1) Haber process
Ignore heat losses
• the bond energies in the table are mean / not specific to
ammonia (1)
Question
Answer Mark
Number
9(a)(iii) The only correct answer is D (100 %) (1)
A is not correct because this is the percentage of hydrogen
B is not correct because this is half the atom economy for making ammonia
C is not correct because this is the percentage of nitrogen
Question
Answer Mark
Number
9(a)(iv) The only correct answer is C (1)
A is not correct because this expression shows molar quantities, not powers and is inverted
B is not correct because this expression shows molar quantities, not powers
D is not correct because this expression is for the reverse equation
Number
9(b) An answer that makes reference to any three of the following points: (3)
• the equilibrium position will shift to the right
OR
this will favour forward reaction (1)
• (in an equilibrium) removal of product decreases rate of back
reaction / rate of formation of reactant(s) (1)
• time to attain / reach equilibrium may be too long (1)
• unreacted reactants can be recycled (1)
Number
9(c)(i) An answer that makes reference to the following points: (2)
• provide / overcome the activation energy Do not allow ‘to lower the activation energy’
or
(is slow at room temperature but) accelerates as temperature rises Allow answers that link rise in temperature to rising
(1) rate
• (sufficiently / very) exothermic enough to melt the copper /
break bonds in copper (1)
Number
9(c)(ii) (2)
Allow transition state for intermediate
• intermediate energy level/transition state (1) Ignore type of arrows to and from intermediate
Allow any diagram with a hump shown, with /
without intermediate / transition state label
• product line below level of reactant line and ∆rH / ∆H shown on Do not penalise missing ‘Products’ label
down/ vertical arrow (1) -1
Allow use of ∆rH / -905.2 (kJ mol )
Number
9(c)(iii) An answer that makes reference to any three of the following points: (3)
• reactants adsorb onto catalyst/surface (1) Do not allow absorb
• (there are) active sites on catalyst (surface) (1)
• bonds in reactants weakened / broken
or
reaction takes place (1)
• products desorb from the catalyst/active site (1)
(Total for Question 9 = 17 marks)
Total for paper = 80 marks
How to answer it
Haber Process, Enthalpy and Heterogeneous Catalysis Study Guide
What this question tests
This comprehensive question assesses core AS Chemistry physical chemistry topics: calculating enthalpy changes from mean bond enthalpies, understanding the limitations of bond enthalpy data compared to standard enthalpy of formation, determining atom economy and equilibrium expressions (Kc), applying Le Chatelier's principle to industrial reactor design, interpreting reaction profiles for catalysed reactions, and explaining the mechanism of heterogeneous catalysis on solid metal surfaces.
Enthalpy Change from Mean Bond Enthalpies
📐 Step-by-Step Calculation
- Reactants Bonds Broken: 1 mole of N≡N and 3 moles of H–H.
Energy input = 945 + (3 × 436) = +2253 kJ mol⁻¹ - Products Bonds Formed: 6 moles of N–H bonds (since stoichiometry forms 2NH₃, and each NH₃ has 3 N–H bonds).
Energy release = 6 × 391 = -2346 kJ mol⁻¹ - Overall Enthalpy Change (ΔH):
ΔH = Bonds broken – Bonds formed (or sum of bonds)
-2346 + 2253 = -93 kJ mol⁻¹
❌ Common Calculation Traps
- Stoichiometry errors: Forgetting that 3 moles of H₂ means multiplying the H–H bond energy by 3.
- Product bonds: Forgetting that 2 moles of NH₃ yields 6 N–H bonds in total.
- Sign omission: A positive or missing sign will cost you the final mark. Always include the negative sign for exothermic reactions.
Limitations of Mean Bond Enthalpies
✅ Correct Answers (Any Two)
- The equation calculated in (a)(i) is for the formation of two moles of ammonia (whereas standard enthalpy of formation is defined for one mole).
- Mean bond enthalpies are average values derived from a range of different compounds, not specific to the actual bonding environment within ammonia.
🧠 Exam Technique & Examiner Insight
Examiners note that candidates frequently waste time discussing differing industrial conditions (like temperature and pressure in the Haber process) or heat losses. Stick strictly to definitions and data limitations: stoichiometry differences and average vs. specific bond energies.
Atom Economy and Kc Expressions
✅ Correct Answers
(iii) Atom Economy: D (100%)
Reasoning: The equation N₂(g) + 3H₂(g) ⇌ 2NH₃(g) features only a single product, meaning all reactant atoms are converted into the desired product.
(iv) Equilibrium Expression (Kc): C
Kc = [NH₃]² / ([N₂][H₂]³)
❌ Distractor Analysis
- For (iii): A is hydrogen percentage, B is half atom economy, C is nitrogen percentage.
- For (iv): Option A uses molar quantities instead of concentrations and is inverted; Option B uses square brackets with no powers; Option D is written for the reverse reaction.
Industrial Trade-offs in Reversible Reactions
💡 Key Knowledge: Why remove product early?
- Removing product shifts the equilibrium position to the right (Le Chatelier's principle), favouring the forward reaction to replace what was lost.
- Removing product decreases the rate of the back reaction, maintaining a high net forward rate.
- Waiting to reach equilibrium can take an impractically long time as the reaction slows down near equilibrium.
- Unreacted reactants can be continuously separated and recycled back into the reactor.
🧠 Exam Technique
This is a standard 3-mark industrial chemistry application question. Ensure you write distinct, scientifically rigorous statements covering equilibrium position, reaction rates, and recycling logistics.
Catalyst Activation and Reaction Profiles
✅ (i) Catalyst Warming & Melting
- Warming: To provide/overcome the activation energy (or to speed up the slow room-temperature reaction). Note: Do not write "to lower activation energy" as catalysts provide an alternative pathway with lower Ea, they don't alter the activation energy of the original pathway.
- Melting: The reaction is sufficiently/very exothermic ( ΔH = -905.2 kJ mol⁻¹ ) that the heat released raises the temperature enough to melt the copper.
✅ (ii) Reaction Profile Requirements
- Must show an intermediate peak (transition state/intermediate energy level) higher than the reactants.
- The final products line must be drawn strictly below the reactant line to visually represent the exothermic nature ( ΔH negative ).
- Clearly label ΔH or show a downward vertical arrow from reactants to products.
Heterogeneous Catalysis Mechanism
💡 Step-by-Step Heterogeneous Catalysis
- Adsorption: Reactant molecules ( NH₃ and O₂ ) adsorb onto the active sites on the surface of the catalyst. (Examiner tip: Use "adsorb", not "absorb"!)
- Reaction: Bonds in the reactant molecules are weakened and broken, and new bonds form as the reaction takes place on the surface.
- Desorption: Product molecules ( H₂O and NO ) desorb from the active sites and leave the catalyst surface.
❌ Common Errors
- Writing "absorb" instead of "adsorb" will lose you the first marking point. Adsorption involves surface attachment; absorption involves entering the bulk material.
- Missing the desorption stage at the end of the sequence.
Topics
Physical Chemistry · Organic Chemistry · Inorganic Chemistry · Topic 5: Formulae, Equations and Amounts of Substance · Topic 8: Energetics I · Topic 9: Kinetics I · Topic 10: Equilibrium I · Topic 11: Equilibrium II
Question and mark scheme from the Edexcel A-Level Chemistry examination, AS Paper 2, November 2021. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.