AQA A-Level Chemistry Paper 3, June 2018: Question 9

1 mark · Easy difficulty · Multiple Choice

Identify which reaction equation represents a free-radical termination step.

Practise this question

Question

Question 09 asks 'Which equation represents a termination step?' with 4 options: A shows CH3CH2CH3 + Br• producing CH3C•HCH3 + HBr; B shows ClO• + O3 producing Cl• + 2O2; C shows RO• + CH2=CH2 producing ROCH2C•H2; D shows CH3C•FCl + Cl• producing CH3CFCl2.
Question text

09 Which equation represents a termination step?

[1 mark]

A

B

C

D

Mark scheme

Show the mark scheme Mark scheme for question 09 shows the correct option is D.

09 D

How to answer it

Identifying Steps in Free-Radical Reactions

📋 What this question tests

This question assesses your ability to recognise the three distinct stages of a free-radical mechanism: initiation, propagation, and termination. You need to identify a termination step by tracking the number of unpaired electrons (free radicals) on the reactant and product sides of each equation.

Question 09 • Multiple Choice • [1 Mark]

Classifying Mechanism Steps

Which equation represents a termination step?

✅ Correct Answer

D: CH₃ĊFCl + Cl• → CH₃CFCl₂

A termination step removes free radicals from the reaction mixture. In this step, two radicals collide and combine to form a single, stable non-radical molecule:

Radical + Radical → Molecule

Award 1 mark for selecting D.

💡 Key Knowledge: The "Radical Count" Rule

You can instantly categorise any free-radical step simply by counting the radical dots (•):

  • Initiation: 0 radicals → 2 radicals
    Molecule → Radical + Radical (homolytic fission driven by UV light)
  • Propagation: 1 radical → 1 radical
    Molecule + Radical → New Radical + New Molecule (chain continues)
  • Termination: 2 radicals → 0 radicals
    Radical + Radical → Molecule (chain ends)

🧠 Exam Technique: Analysis of Incorrect Options

  • A: CH₃CH₂CH₃ + Br• → CH₃ĊHCH₃ + HBr
    1 radical on left, 1 radical on right. This is a propagation step (hydrogen abstraction from propane).
  • B: ClO• + O₃ → Cl• + 2O₂
    1 radical on left, 1 radical on right. This is a propagation step in the catalytic destruction of ozone.
  • C: RO• + CH₂=CH₂ → ROCH₂ĊH₂
    1 radical on left, 1 radical on right. This is a propagation step (radical addition to an alkene in polymerisation).

❌ Common Errors & Pitfalls

  • Confusing C for termination: Students often see two reactants joining to form one product and assume it is termination. However, the product in C is still a radical ( ROCH₂ĊH₂ ), meaning the chain reaction is still active!
  • Misidentifying ozone depletion steps: Reactions involving ClO• often cause confusion. Remember that because a chlorine radical ( Cl• ) is regenerated, step B is propagation, allowing chlorine to act as a catalyst.
  • Overlooking the radical dot: Always scan both sides of the arrow carefully to count the total number of single dots representing unpaired electrons.

Topics

Organic Chemistry · 3.3.1 Introduction to Organic Chemistry · 3.3.2 Alkanes · 3.3.3 Halogenoalkanes

Question and mark scheme from the AQA A-Level Chemistry examination, Paper 3, June 2018. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.