Question Simulator

IGCSE Chemistry (0620)

Chemical energetics Banker

118 questions · about 3% of the marks we indexed · examined in 9 of 9 sessions.

Questions by year

2026

  • 2026 May/June · Paper 11 · Q141 markEnergy profiles & activation energy
  • 2026 May/June · Paper 12 · Q131 markExothermic & endothermic
  • 2026 May/June · Paper 13 · Q141 markExothermic & endothermic
  • 2026 May/June · Paper 21 · Q151 markExothermic & endothermic
  • 2026 May/June · Paper 21 · Q161 markEnergy profiles & activation energy
  • 2026 May/June · Paper 22 · Q141 markBond-energy calculations
  • 2026 May/June · Paper 23 · Q171 markBond-energy calculations
  • 2026 May/June · Paper 23 · Q201 markEnergy profiles & activation energy
  • 2026 May/June · Paper 42 · Q5 (c(i), c(ii), c(iii))9 marksBond-energy calculations · Energy profiles & activation energy · Exothermic & endothermic
  • 2026 May/June · Paper 61 · Q2 (c)1 markExothermic & endothermic
  • 2026 May/June · Paper 63 · Q2 (f)1 markExothermic & endothermic

2025

  • 2025 Oct/Nov · Paper 11 · Q121 markExothermic & endothermic
  • 2025 Oct/Nov · Paper 11 · Q131 markEnergy profiles & activation energy
  • 2025 Oct/Nov · Paper 12 · Q141 markExothermic & endothermic
  • 2025 Oct/Nov · Paper 13 · Q141 markEnergy profiles & activation energy
  • 2025 Oct/Nov · Paper 21 · Q141 markExothermic & endothermic
  • 2025 Oct/Nov · Paper 21 · Q151 markEnergy profiles & activation energy
  • 2025 Oct/Nov · Paper 22 · Q141 markBond-energy calculations
  • 2025 Oct/Nov · Paper 22 · Q151 markExothermic & endothermic
  • 2025 Oct/Nov · Paper 23 · Q161 markEnergy profiles & activation energy
  • 2025 Oct/Nov · Paper 23 · Q171 markBond-energy calculations
  • 2025 Oct/Nov · Paper 31 · Q8 (c)2 marksEnergy profiles & activation energy
  • 2025 Oct/Nov · Paper 32 · Q8 (c)2 marksEnergy profiles & activation energy
  • 2025 Oct/Nov · Paper 33 · Q8 (d)2 marksEnergy profiles & activation energy
  • 2025 Oct/Nov · Paper 41 · Q4 (a, b)8 marksBond-energy calculations · Energy profiles & activation energy
  • 2025 Oct/Nov · Paper 43 · Q3 (c(i), c(ii))2 marksExothermic & endothermic
  • 2025 Oct/Nov · Paper 43 · Q4 (b)3 marksBond-energy calculations
  • 2025 Oct/Nov · Paper 63 · Q2 (c)2 marksExothermic & endothermic
  • 2025 May/June · Paper 11 · Q131 markExothermic & endothermic
  • 2025 May/June · Paper 12 · Q141 markEnergy profiles & activation energy
  • 2025 May/June · Paper 13 · Q131 markExothermic & endothermic
  • 2025 May/June · Paper 21 · Q131 markExothermic & endothermic
  • 2025 May/June · Paper 22 · Q131 markEnergy profiles & activation energy
  • 2025 May/June · Paper 22 · Q141 markBond-energy calculations
  • 2025 May/June · Paper 23 · Q111 markExothermic & endothermic
  • 2025 May/June · Paper 23 · Q131 markExothermic & endothermic
  • 2025 May/June · Paper 23 · Q141 markEnergy profiles & activation energy
  • 2025 May/June · Paper 31 · Q7 (a(i), a(iii))3 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2025 May/June · Paper 32 · Q7 (c(i), c(ii), c(iv))4 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2025 May/June · Paper 33 · Q6 (b(i), b(ii), b(iii))4 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2025 May/June · Paper 41 · Q6 (d(ii))3 marksBond-energy calculations
  • 2025 May/June · Paper 43 · Q6 (e(iii))3 marksBond-energy calculations
  • 2025 May/June · Paper 52 · Q1 (d)1 markExothermic & endothermic
  • 2025 May/June · Paper 62 · Q2 (d)1 markExothermic & endothermic

2024

  • 2024 Oct/Nov · Paper 11 · Q121 markEnergy profiles & activation energy
  • 2024 Oct/Nov · Paper 11 · Q131 markExothermic & endothermic
  • 2024 Oct/Nov · Paper 12 · Q141 markExothermic & endothermic
  • 2024 Oct/Nov · Paper 13 · Q131 markEnergy profiles & activation energy
  • 2024 Oct/Nov · Paper 13 · Q141 markExothermic & endothermic
  • 2024 Oct/Nov · Paper 21 · Q141 markEnergy profiles & activation energy
  • 2024 Oct/Nov · Paper 22 · Q141 markEnergy profiles & activation energy
  • 2024 Oct/Nov · Paper 23 · Q141 markEnergy profiles & activation energy
  • 2024 Oct/Nov · Paper 23 · Q151 markBond-energy calculations
  • 2024 Oct/Nov · Paper 31 · Q7 (b(i), b(ii))3 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2024 Oct/Nov · Paper 32 · Q7 (b(iii), b(iv))2 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2024 Oct/Nov · Paper 33 · Q7 (c(i), c(ii), c(iii))3 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2024 Oct/Nov · Paper 42 · Q3 (e(i), e(ii))2 marksEnergy profiles & activation energy
  • 2024 Oct/Nov · Paper 63 · Q2 (c)1 markExothermic & endothermic
  • 2024 May/June · Paper 11 · Q121 markOfficial paper ↗Exothermic & endothermic
  • 2024 May/June · Paper 12 · Q151 markExothermic & endothermic
  • 2024 May/June · Paper 13 · Q141 markEnergy profiles & activation energy
  • 2024 May/June · Paper 21 · Q151 markOfficial paper ↗Bond-energy calculations
  • 2024 May/June · Paper 21 · Q161 markOfficial paper ↗Energy profiles & activation energy
  • 2024 May/June · Paper 22 · Q121 markEnergy profiles & activation energy
  • 2024 May/June · Paper 23 · Q121 markExothermic & endothermic
  • 2024 May/June · Paper 23 · Q131 markExothermic & endothermic
  • 2024 May/June · Paper 23 · Q141 markEnergy profiles & activation energy
  • 2024 May/June · Paper 33 · Q6 (e)1 markExothermic & endothermic
  • 2024 May/June · Paper 41 · Q4 (e(iii))1 markOfficial paper ↗Energy profiles & activation energy
  • 2024 May/June · Paper 42 · Q3 (b, e)4 marksBond-energy calculations · Exothermic & endothermic

2023

  • 2023 Oct/Nov · Paper 11 · Q111 markEnergy profiles & activation energy
  • 2023 Oct/Nov · Paper 12 · Q131 markExothermic & endothermic
  • 2023 Oct/Nov · Paper 13 · Q131 markExothermic & endothermic
  • 2023 Oct/Nov · Paper 21 · Q101 markEnergy profiles & activation energy
  • 2023 Oct/Nov · Paper 21 · Q111 markBond-energy calculations
  • 2023 Oct/Nov · Paper 22 · Q121 markExothermic & endothermic
  • 2023 Oct/Nov · Paper 22 · Q131 markExothermic & endothermic
  • 2023 Oct/Nov · Paper 22 · Q141 markBond-energy calculations
  • 2023 Oct/Nov · Paper 23 · Q131 markExothermic & endothermic
  • 2023 Oct/Nov · Paper 23 · Q141 markBond-energy calculations
  • 2023 Oct/Nov · Paper 33 · Q5 (b(iii))2 marksExothermic & endothermic
  • 2023 Oct/Nov · Paper 42 · Q5 (a, b(iii), b(iv), b(v), c)11 marksBond-energy calculations · Energy profiles & activation energy · Exothermic & endothermic
  • 2023 Oct/Nov · Paper 61 · Q2 (g)2 marksExothermic & endothermic
  • 2023 May/June · Paper 11 · Q111 markEnergy profiles & activation energy
  • 2023 May/June · Paper 12 · Q111 markExothermic & endothermic
  • 2023 May/June · Paper 13 · Q111 markExothermic & endothermic
  • 2023 May/June · Paper 21 · Q111 markBond-energy calculations
  • 2023 May/June · Paper 22 · Q111 markBond-energy calculations
  • 2023 May/June · Paper 23 · Q121 markEnergy profiles & activation energy
  • 2023 May/June · Paper 23 · Q131 markBond-energy calculations
  • 2023 May/June · Paper 31 · Q4 (c(i), c(ii), c(iii))3 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2023 May/June · Paper 32 · Q4 (c(i), c(ii), c(iii))4 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2023 May/June · Paper 33 · Q4 (b(i), b(ii), b(iii))3 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2023 May/June · Paper 63 · Q2 (c)1 markExothermic & endothermic

2022

  • 2022 Oct/Nov · Paper 11 · Q111 markExothermic & endothermic
  • 2022 Oct/Nov · Paper 12 · Q111 markExothermic & endothermic
  • 2022 Oct/Nov · Paper 13 · Q111 markExothermic & endothermic
  • 2022 Oct/Nov · Paper 21 · Q111 markExothermic & endothermic
  • 2022 Oct/Nov · Paper 21 · Q131 markBond-energy calculations
  • 2022 Oct/Nov · Paper 22 · Q111 markExothermic & endothermic
  • 2022 Oct/Nov · Paper 23 · Q111 markExothermic & endothermic
  • 2022 Oct/Nov · Paper 23 · Q171 markBond-energy calculations
  • 2022 Oct/Nov · Paper 31 · Q3 (c)1 markExothermic & endothermic
  • 2022 Oct/Nov · Paper 32 · Q3 (a, d)2 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2022 Oct/Nov · Paper 41 · Q5 (d(i), d(ii))6 marksBond-energy calculations · Energy profiles & activation energy
  • 2022 Oct/Nov · Paper 42 · Q5 (e(i), e(ii), e(iii), f)6 marksBond-energy calculations · Energy profiles & activation energy
  • 2022 Oct/Nov · Paper 43 · Q6 (a(i), a(ii))4 marksBond-energy calculations · Exothermic & endothermic
  • 2022 May/June · Paper 11 · Q131 markExothermic & endothermic
  • 2022 May/June · Paper 12 · Q111 markExothermic & endothermic
  • 2022 May/June · Paper 13 · Q111 markEnergy profiles & activation energy
  • 2022 May/June · Paper 21 · Q131 markBond-energy calculations
  • 2022 May/June · Paper 22 · Q151 markExothermic & endothermic
  • 2022 May/June · Paper 22 · Q161 markEnergy profiles & activation energy
  • 2022 May/June · Paper 31 · Q4 (d(i), d(ii))2 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2022 May/June · Paper 32 · Q4 (d(i), d(ii))2 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2022 May/June · Paper 33 · Q4 (c(ii), c(iii))2 marksEnergy profiles & activation energy · Exothermic & endothermic
  • 2022 May/June · Paper 41 · Q7 (e)3 marksBond-energy calculations
  • 2022 May/June · Paper 61 · Q2 (f(i))1 markExothermic & endothermic

References only, not question text. Open Official paper ↗ where Cambridge publishes the paper, or see the official Cambridge past-papers page; for other papers, ask your school. “Paper 42” means Paper 4, variant 2.

Practice questions

Original questions written by HomiLabs in the style of the exam, with answers and mark schemes. They are not Cambridge past paper questions and have not been reviewed by Cambridge. Try each one before opening the answer.

Q1Energy profiles & activation energy · Core · Paper 2 style · 1 mark
  1. (a) Which statement is correct for the energy profile of an exothermic reaction? [1]
Show answer
  1. (a) B The products are at a lower energy level than the reactants.
    Exothermic: energy is given out, so the products end lower than the reactants. All reactions have an activation energy.
Q2Energy profiles & activation energy · Core · Paper 4 style · 4 marks
  1. (a) Define activation energy, Ea. [1]
  2. (b) Describe the energy profile for an endothermic reaction. Say where the reactants and products are, and show how Ea and ΔH are measured. [3]
Show answer
  1. (a) The minimum energy that colliding particles must have in order to react.
    B1
  2. (b) Products higher than reactants; curve rises to a peak above both; Ea = height from reactants to peak; ΔH = difference from reactants to products (upward, positive).
    B1 products above reactants; B1 Ea from reactants to peak; B1 ΔH reactants to products.
Q3Energy profiles & activation energy · Standard · Paper 2 style · 1 mark
  1. (a) On an energy profile, the reactants are at 120 kJ/mol, the top of the curve is at 290 kJ/mol and the products are at 40 kJ/mol. What are the activation energy and the enthalpy change, ΔH? [1]
Show answer
  1. (a) A activation energy 170 kJ/mol, ΔH −80 kJ/mol
    Ea = 290 − 120 = 170 kJ/mol; ΔH = 40 − 120 = −80 kJ/mol. B measures Ea from the products.
Q4Energy profiles & activation energy · Standard · Paper 4 style · 4 marks

A reaction has ΔH = +58 kJ/mol and activation energy Ea = 140 kJ/mol.

  1. (a) Is the reaction exothermic or endothermic? Give a reason. [1]
  2. (b) Calculate the energy of the top of the curve relative to the products. [2]
  3. (c) State the activation energy of the reverse reaction. [1]
Show answer
  1. (a) Endothermic, because ΔH is positive.
    B1
  2. (b) 82 kJ/mol
    M1 Ea − ΔH; A1 140 − 58 = 82
  3. (c) 82 kJ/mol
    B1
Q5Energy profiles & activation energy · Standard · Paper 4 style · 3 marks

Many homes in Pakistan cook on piped natural gas (mainly methane).

  1. (a) The burning of natural gas is exothermic, yet a gas stove needs a spark or match to light it. Explain why. [2]
  2. (b) Explain why the flame keeps burning once it has been lit. [1]
Show answer
  1. (a) The reaction has an activation energy; the spark supplies energy so particles collide with energy at least equal to Ea.
    B1 activation energy; B1 spark supplies it.
  2. (b) The energy released by the reaction supplies the activation energy for more molecules to react.
    B1
Q6Energy profiles & activation energy · Standard · Paper 4 style · 4 marks

Hydrogen peroxide decomposes slowly to water and oxygen. When a little manganese(IV) oxide is added, the reaction becomes much faster.

  1. (a) Describe how the energy profile for the catalysed reaction differs from that for the uncatalysed reaction. [2]
  2. (b) Hydrogen peroxide decomposition is exothermic. State where the products are on the energy profile. [1]
  3. (c) State what happens to the mass of manganese(IV) oxide during the reaction. [1]
Show answer
  1. (a) The peak is lower (lower activation energy); the reactant and product levels are the same (same ΔH).
    B1 lower peak; B1 same start and end levels.
  2. (b) Below the reactants.
    B1
  3. (c) It stays the same (the catalyst is not used up).
    B1
Q7Energy profiles & activation energy · Challenge · Paper 2 style · 1 mark
  1. (a) [1]
Show answer
  1. (a) B activation energy decreases, ΔH unchanged
    A catalyst gives an alternative pathway with lower activation energy; the energies of reactants and products are unchanged, so ΔH is unchanged.
Q8Energy profiles & activation energy · Challenge · Paper 4 style · 6 marks

An energy profile is described by these points (energy in kJ/mol):reactants 50; top of curve 230; products 180.

  1. (a) Calculate ΔH for the forward reaction. [1]
  2. (b) Calculate the activation energy of the uncatalysed forward reaction. [1]
  3. (c) With a catalyst the peak is at 150 kJ/mol. Calculate the new activation energy. [1]
  4. (d) Calculate the activation energy of the uncatalysed reverse reaction. [1]
  5. (e) Explain why the catalysed reaction is faster. [2]
Show answer
  1. (a) +130 kJ/mol
    B1 180 − 50
  2. (b) 180 kJ/mol
    B1 230 − 50
  3. (c) 100 kJ/mol
    B1 150 − 50
  4. (d) 50 kJ/mol
    B1 230 − 180
  5. (e) More of the colliding particles have energy equal to or greater than the lower activation energy, so there are more successful collisions per second.
    B1 lower Ea; B1 more successful collisions per unit time.
Q9Energy profiles & activation energy · Challenge · Paper 4 style · 5 marks

Data for four reactions:Reaction P: Ea 95 kJ/mol, ΔH −210 kJ/molReaction Q: Ea 40 kJ/mol, ΔH −60 kJ/molReaction R: Ea 180 kJ/mol, ΔH −390 kJ/molReaction S: Ea 120 kJ/mol, ΔH +45 kJ/mol

  1. (a) Which reaction would be fastest at room temperature? Explain. [2]
  2. (b) Which reaction is endothermic? [1]
  3. (c) For reaction P, calculate the activation energy of the reverse reaction. [1]
  4. (d) Which reaction gives out the most energy when 1 mole reacts? [1]
Show answer
  1. (a) Reaction Q; it has the lowest activation energy, so the greatest proportion of collisions have enough energy to react.
    B1 Q; B1 lowest Ea.
  2. (b) Reaction S
    B1 positive ΔH
  3. (c) 305 kJ/mol
    B1 95 + 210
  4. (d) Reaction R (−390 kJ/mol)
    B1
Q10Exothermic & endothermic · Core · Paper 2 style · 1 mark
  1. (a) Which process is endothermic? [1]
Show answer
  1. (a) C thermal decomposition of calcium carbonate
    Thermal decomposition needs continuous heating – energy is taken in. Combustion, neutralisation and respiration all release energy.
Q11Exothermic & endothermic · Core · Paper 6 style · 4 marks

A student mixed 25 cm³ of dilute hydrochloric acid with 25 cm³ of aqueous sodium hydroxide in a polystyrene cup. Initial temperature of both solutions = 22.5 °C; highest temperature reached = 29.0 °C.

  1. (a) Calculate the temperature rise. [1]
  2. (b) State whether the reaction is exothermic or endothermic. Give a reason. [1]
  3. (c) Suggest why a polystyrene cup is used instead of a glass beaker. [1]
  4. (d) Suggest one further improvement to make the temperature rise more accurate. [1]
Show answer
  1. (a) 6.5 °C
    B1 29.0 − 22.5
  2. (b) Exothermic, because the temperature rose.
    B1
  3. (c) Polystyrene is a good insulator, so less heat is lost to the surroundings.
    B1
  4. (d) Put a lid on the cup / use a thermometer reading to 0.1 °C / stir / repeat and average.
    B1
Q12Exothermic & endothermic · Core · Paper 4 style · 5 marks
  1. (a) Classify each change as exothermic or endothermic.(i) burning petrol in a car engine(ii) electrolysis of molten aluminium oxide(iii) adding magnesium to dilute hydrochloric acid(iv) melting ice [4]
  2. (b) Define an exothermic reaction in terms of energy transfer. [1]
Show answer
  1. (a) (i) exothermic (ii) endothermic (iii) exothermic (iv) endothermic
    B1 each.
  2. (b) A reaction that transfers thermal energy to the surroundings, so the temperature of the surroundings increases.
    B1
Q13Exothermic & endothermic · Standard · Paper 2 style · 1 mark
  1. (a) When ammonium nitrate dissolves in water, the temperature of the solution falls from 21 °C to 13 °C. Which statement explains this? [1]
Show answer
  1. (a) B The process is endothermic; energy is transferred from the surroundings.
    A fall in temperature shows thermal energy is taken in from the surroundings (the water), so the process is endothermic.
Q14Exothermic & endothermic · Standard · Paper 5 style · 6 marks

A student dissolved 5.0 g of each salt in 50 cm³ of water and recorded the temperatures.Ammonium chloride: start 21.0 °C, end 16.5 °CCalcium chloride (anhydrous): start 21.0 °C, end 32.0 °CPotassium nitrate: start 21.5 °C, end 15.5 °CSodium chloride: start 21.0 °C, end 20.5 °C

  1. (a) Calculate the temperature change for each salt. Use + for a rise and − for a fall. [2]
  2. (b) Which salt dissolves in the most endothermic process? [1]
  3. (c) Which salt would be most suitable for a self-heating food can? Explain. [1]
  4. (d) Give two variables that should be kept constant. [2]
Show answer
  1. (a) Ammonium chloride −4.5 °C; calcium chloride +11.0 °C; potassium nitrate −6.0 °C; sodium chloride −0.5 °C
    2 marks all four; 1 mark for two or three.
  2. (b) Potassium nitrate
    B1 largest fall
  3. (c) Calcium chloride; it dissolves exothermically, giving the largest rise.
    B1
  4. (d) Mass of salt; volume of water; starting temperature of water; type of container.
    1 mark each for any two.
Q15Exothermic & endothermic · Standard · Paper 4 style · 5 marks
  1. (a) A physiotherapist at a cricket match uses an instant cold pack. Squeezing it lets ammonium nitrate dissolve in water. Explain how this cools the injury. [2]
  2. (b) A hand warmer contains iron powder that reacts with oxygen from the air. State whether this reaction is exothermic or endothermic, and describe the energy transfer. [2]
  3. (c) Suggest why the iron in the hand warmer is a fine powder rather than a lump. [1]
Show answer
  1. (a) Dissolving is endothermic; it takes in thermal energy from the surroundings (the injured skin), lowering its temperature.
    B1 endothermic; B1 energy taken from surroundings/skin.
  2. (b) Exothermic; thermal energy is transferred from the reacting chemicals to the surroundings (hands).
    B1 exothermic; B1 energy to surroundings.
  3. (c) Larger surface area so it reacts faster and releases heat quickly.
    B1
Q16Exothermic & endothermic · Challenge · Paper 5 style · 6 marks

Excess zinc powder was added to 50 cm³ of aqueous copper(II) sulfate in an insulated cup at time 0. The temperature was recorded every 30 seconds.Time/min: 0.0, 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5Temperature/°C: 21.0, 27.5, 32.0, 34.0, 34.5, 34.0, 33.5, 33.0

  1. (a) Calculate the maximum temperature rise. [1]
  2. (b) Explain why the temperature falls after 2.0 minutes. [1]
  3. (c) Write the ionic equation for the reaction. [1]
  4. (d) The experiment is repeated with magnesium powder instead of zinc, using the same number of moles of metal. Predict how the maximum temperature rise would compare. Explain. [2]
  5. (e) Suggest why zinc was used in excess. [1]
Show answer
  1. (a) 13.5 °C
    B1 34.5 − 21.0
  2. (b) The reaction has finished and heat is lost to the surroundings.
    B1
  3. (c) Zn(s) + Cu²⁺(aq) → Zn²⁺(aq) + Cu(s)
    B1
  4. (d) Larger rise; magnesium is further above copper in the reactivity series, so more energy is released.
    B1 larger; B1 magnesium more reactive.
  5. (e) So that all the copper(II) ions react / the temperature rise depends only on the amount of copper(II) sulfate.
    B1
Q17Exothermic & endothermic · Challenge · Paper 4 style · 6 marks

Respiration: C₆H₁₂O₆ + 6O₂ → 6CO₂ + 6H₂O ΔH = −2800 kJ/mol

  1. (a) State the value of ΔH for photosynthesis, 6CO₂ + 6H₂O → C₆H₁₂O₆ + 6O₂, and say whether it is exothermic or endothermic. [2]
  2. (b) Calculate the energy released per gram of glucose in respiration. [Mr glucose = 180] Give your answer to 3 significant figures. [1]
  3. (c) Describe the energy level diagram for respiration. [2]
  4. (d) State where the energy for photosynthesis comes from. [1]
Show answer
  1. (a) +2800 kJ/mol; endothermic
    B1 +2800; B1 endothermic.
  2. (b) 15.6 kJ/g
    B1 2800 ÷ 180
  3. (c) Reactants (glucose + oxygen) at a higher level than products (carbon dioxide + water); downward arrow labelled ΔH = −2800 kJ/mol.
    B1 products lower; B1 ΔH labelled negative.
  4. (d) Light (from the Sun).
    B1
Q18Bond-energy calculations · Core · Paper 4 style · 4 marks

At the high temperatures inside a car engine, nitrogen reacts with oxygen: N≡N + O=O → 2 N=OBond energies in kJ/mol: N≡N 945, O=O 498, N=O 630

  1. (a) Calculate the energy needed to break the bonds in the reactants. [1]
  2. (b) Calculate the energy released when the bonds in the products form. [1]
  3. (c) Calculate the energy change, ΔH, for the reaction and state whether it is exothermic or endothermic. [2]
Show answer
  1. (a) 1443 kJ
    B1 945 + 498
  2. (b) 1260 kJ
    B1 2 × 630
  3. (c) ΔH = +183 kJ/mol; endothermic
    M1 1443 − 1260; A1 +183 kJ/mol with endothermic (more energy taken in to break bonds than released making bonds).
Q19Bond-energy calculations · Core · Paper 4 style · 4 marks

In the Haber process: N≡N + 3 H–H ⇌ 2NH₃ (each NH₃ has three N–H bonds)Bond energies in kJ/mol: N≡N 945, H–H 436, N–H 391

  1. (a) Calculate the energy change, ΔH, for the reaction in kJ/mol. [3]
  2. (b) State the sign of ΔH for the reverse reaction, the decomposition of ammonia. [1]
Show answer
  1. (a) −93 kJ/mol
    M1 broken: 945 + 3 × 436 = 2253; M1 formed: 6 × 391 = 2346; A1 2253 − 2346 = −93
  2. (b) Positive (+93 kJ/mol, endothermic).
    B1
Q20Bond-energy calculations · Core · Paper 2 style · 1 mark
  1. (a) Which statement about bond energies is correct? [1]
Show answer
  1. (a) B Breaking bonds takes in energy and making bonds releases energy.
    Energy must be supplied to pull atoms apart (endothermic); energy is released when bonds form (exothermic). A is the common reversal.
Q21Bond-energy calculations · Core · Paper 4 style · 4 marks

For a reaction, the total energy taken in to break bonds is 1850 kJ/mol and the total energy released in making bonds is 2100 kJ/mol.

  1. (a) Calculate ΔH for the reaction. [1]
  2. (b) State whether the reaction is exothermic or endothermic and explain your answer. [2]
  3. (c) State what happens to the temperature of the surroundings during the reaction. [1]
Show answer
  1. (a) −250 kJ/mol
    B1 1850 − 2100
  2. (b) Exothermic; more energy is released in making bonds than is taken in to break bonds (ΔH negative).
    B1 exothermic; B1 explanation.
  3. (c) It rises.
    B1
Q22Bond-energy calculations · Standard · Paper 4 style · 5 marks

Natural gas (methane) burns in a gas stove:CH₄ + 2O₂ → CO₂ + 2H₂OBond energies in kJ/mol: C–H 413, O=O 498, C=O 805, O–H 464

  1. (a) Calculate the total energy needed to break all the bonds in the reactants. [1]
  2. (b) Calculate the total energy released when the bonds in the products form. [1]
  3. (c) Calculate the energy change for the reaction, in kJ/mol. [1]
  4. (d) Explain, in terms of bond breaking and bond making, why this reaction is exothermic. [2]
Show answer
  1. (a) 2648 kJ
    B1 4 × 413 + 2 × 498
  2. (b) 3466 kJ
    B1 2 × 805 + 4 × 464
  3. (c) −818 kJ/mol
    B1 2648 − 3466
  4. (d) More energy is released when the new bonds in CO₂ and H₂O form than is taken in to break the bonds in CH₄ and O₂.
    B1 bond breaking takes in energy, bond making releases energy; B1 more released than taken in.
Q23Bond-energy calculations · Standard · Paper 2 style · 1 mark
  1. (a) Hydrogen iodide decomposes: 2HI → H₂ + I₂Bond energies in kJ/mol: H–I 299, H–H 436, I–I 151What is the energy change for this reaction? [1]
Show answer
  1. (a) B +11 kJ/mol
    Broken: 2 × 299 = 598; formed: 436 + 151 = 587; ΔH = 598 − 587 = +11 kJ/mol (endothermic). A has the sign reversed (formed − broken).
Q24Bond-energy calculations · Standard · Paper 4 style · 5 marks

A city plans hydrogen-powered buses. Hydrogen burns in oxygen to form water.Bond energies in kJ/mol: H–H 436, O=O 498, O–H 464

  1. (a) Calculate ΔH for the reaction 2H₂ + O₂ → 2H₂O in kJ/mol. [3]
  2. (b) Calculate the energy released per mole of hydrogen, H₂, burned. [1]
  3. (c) State one advantage of hydrogen as a fuel for buses. [1]
Show answer
  1. (a) −486 kJ/mol
    M1 broken 2 × 436 + 498 = 1370; M1 formed 4 × 464 = 1856; A1 −486
  2. (b) 243 kJ
    B1 486 ÷ 2
  3. (c) The only product is water (no carbon dioxide).
    B1
Q25Bond-energy calculations · Standard · Paper 4 style · 4 marks

Methane reacts with chlorine: CH₄ + Cl₂ → CH₃Cl + HClBond energies in kJ/mol: C–H 413, Cl–Cl 242, C–Cl 327, H–Cl 431

  1. (a) Calculate ΔH for this reaction in kJ/mol. [3]
  2. (b) State the condition needed for this reaction to happen. [1]
Show answer
  1. (a) −103 kJ/mol
    M1 broken (one C–H and Cl–Cl): 413 + 242 = 655; M1 formed C–Cl 327 + H–Cl 431 = 758; A1 −103
  2. (b) Ultraviolet light.
    B1
Q26Bond-energy calculations · Standard · Paper 4 style · 6 marks

Bond energies in kJ/mol: H–H 436, F–F 158, H–F 568, Cl–Cl 242, H–Cl 431

  1. (a) Calculate ΔH for H₂ + F₂ → 2HF in kJ/mol. [2]
  2. (b) Calculate ΔH for H₂ + Cl₂ → 2HCl in kJ/mol. [2]
  3. (c) Which reaction releases more energy? Use the bond energies to explain why. [2]
Show answer
  1. (a) −542 kJ/mol
    M1 broken 436 + 158 = 594, formed 2 × 568 = 1136; A1 −542
  2. (b) −184 kJ/mol
    M1 678 − 862; A1 −184
  3. (c) Hydrogen with fluorine; the F–F bond is weak (easy to break) and the H–F bond is very strong (much energy released on forming).
    B1 fluorine reaction; B1 reference to weak F–F and/or strong H–F.
Q27Bond-energy calculations · Challenge · Paper 4 style · 4 marks

Ethene reacts with hydrogen using a nickel catalyst: CH₂=CH₂ + H–H → CH₃–CH₃Bond energies in kJ/mol: C=C 612, C–C 347, C–H 413, H–H 436

  1. (a) Calculate ΔH for the reaction, in kJ/mol. [3]
  2. (b) Suggest why bond-energy calculations give only an approximate value of ΔH. [1]
Show answer
  1. (a) −125 kJ/mol
    M1 broken C=C 612 + H–H 436 = 1048 (C–H unchanged); M1 formed C–C 347 + 2 × C–H 826 = 1173; A1 −125. (Counting all bonds gives the same answer.)
  2. (b) Bond energies are average values taken from many different compounds.
    B1
Q28Bond-energy calculations · Challenge · Paper 4 style · 4 marks

H₂ + Br₂ → 2HBr ΔH = −103 kJ/molBond energies in kJ/mol: H–H 436, Br–Br 193

  1. (a) Calculate the bond energy of the H–Br bond. [3]
  2. (b) Is the H–Br bond stronger or weaker than the H–Cl bond (431 kJ/mol)? Explain. [1]
Show answer
  1. (a) 366 kJ/mol
    M1 ΔH = broken − formed so −103 = (436 + 193) − 2x; M1 2x = 732; A1 x = 366
  2. (b) Weaker; less energy is needed to break it.
    B1
Q29Bond-energy calculations · Challenge · Paper 4 style · 5 marks

Ethanol, CH₃CH₂OH, is used as a fuel in some countries:C₂H₅OH + 3O₂ → 2CO₂ + 3H₂OEthanol contains 5 C–H, 1 C–C, 1 C–O and 1 O–H bond.Bond energies in kJ/mol: C–H 413, C–C 347, C–O 358, O–H 464, O=O 498, C=O 805

  1. (a) Calculate the energy needed to break all the bonds in one mole of ethanol and three moles of oxygen. [2]
  2. (b) Calculate ΔH for the combustion of ethanol in kJ/mol. [2]
  3. (c) Calculate the energy released per gram of ethanol. [Mr ethanol = 46] Give your answer to 3 significant figures. [1]
Show answer
  1. (a) 4728 kJ
    M1 ethanol: 5 × 413 + 347 + 358 + 464 = 3234; A1 + 3 × 498 = 4728
  2. (b) −1276 kJ/mol
    M1 formed: 4 × 805 + 6 × 464 = 6004; A1 4728 − 6004 = −1276
  3. (c) 27.7 kJ/g
    B1 1276 ÷ 46
Q30Bond-energy calculations · Challenge · Paper 4 style · 5 marks

Hydrogen peroxide decomposes: 2H–O–O–H → 2H–O–H + O=OBond energies in kJ/mol: O–H 464, O–O 146, O=O 498

  1. (a) Calculate ΔH for this reaction in kJ/mol. [3]
  2. (b) The value measured by experiment is −196 kJ/mol. Suggest why the calculated value is different. [1]
  3. (c) Manganese(IV) oxide speeds up this reaction. State its effect on the value of ΔH. [1]
Show answer
  1. (a) −206 kJ/mol
    M1 broken: 2 × (2 × 464 + 146) = 2148; M1 formed: 4 × 464 + 498 = 2354; A1 −206
  2. (b) Bond energies are average values / the substances are not all gases in the experiment.
    B1
  3. (c) No effect (ΔH unchanged).
    B1

Similar questions

Questions that test the same subtopic in different years, grouped so you can work on one skill at a time.

References only: find each question in its paper (official link where available, otherwise through your school).

Energy profiles & activation energy Banker48 questions · 9/9 sessions
Exothermic & endothermic Banker65 questions · 9/9 sessions
Bond-energy calculations Banker27 questions · 9/9 sessions

Subtopics

Our analysis of how often each subtopic was examined and how many marks it carried, 2022 to May/June 2026.

SubtopicMarks indexedSessions
Energy profiles & activation energy Banker749/9
Exothermic & endothermic Banker739/9
Bond-energy calculations Banker529/9

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