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A Level · Cambridge (CIE) · 9701

Describe alkane substitution by chlorine and bromine

Describe UV-initiated halogen substitution in alkanes using ethane as the example.

Section 14 · Hydrocarbons

Hydrocarbons · Cambridge 9701 AS Chemistry · 14.1

AS Level; Cambridge International Chemistry 9701, 2025–2027 syllabus. Apply the stated reagents and conditions, balance equations, and keep mechanistic claims within the named examples. Written practice is self-checked

Before you begin

  • Use displayed and structural formulas, covalent bond polarity, balanced equations, and the organic reaction terms from Topic 13.

Work on paper. Try each question before revealing help, and explain why your method works.

Quick readiness check

What is replaced in alkane halogenation?

What you will learn

  • Recognise substitution of an alkane hydrogen
  • Use chlorine or bromine and ultraviolet light
  • Write a monohalogenation equation

A hydrogen atom can be replaced by a halogen

Alkanes react with chlorine or bromine under ultraviolet light by free-radical substitution. In ethane, one hydrogen can be replaced to form chloroethane or bromoethane, together with a hydrogen halide.

C₂H₆ + Cl₂ → C₂H₅Cl + HCl is a balanced example. UV light provides energy to initiate the radical chain; it is a condition, not a reactant in the balanced equation.

Substitution can continue

The first halogenoalkane can undergo further substitution, so a reaction mixture can contain products with more than one halogen atom and multiple positional isomers for longer chains.

The single-substitution equation is a representative step. Avoid promising a pure monohalogenated product unless the question supplies conditions or separation evidence.

Pause and explain

Which condition initiates alkane substitution by Cl₂ or Br₂?

Put the idea to work

Worked example

Describe the reaction of ethane with bromine in ultraviolet light and give a balanced equation for one substitution.

Show the worked solution
  1. Identify this as free-radical substitution.
  2. Replace one ethane hydrogen with bromine.
  3. The displaced hydrogen forms HBr.

Answer C₂H₆ + Br₂ → C₂H₅Br + HBr, in ultraviolet light.

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From guided practice to a new situation

Write your answer and reasoning first. Use a hint only if you are stuck. The model solution is for self-checking; your written work is not automatically marked.

1 · Guided

Write the balanced equation for one hydrogen in ethane being replaced by chlorine.

Give me a hint

Replace H with Cl and account for the displaced H in the other product.

Compare my reasoning
  1. Ethane loses one H to become C₂H₅Cl.
  2. Cl₂ supplies the replacing Cl and the HCl chlorine.
  3. Check C, H and Cl counts.

C₂H₆ + Cl₂ → C₂H₅Cl + HCl (UV light).

Look for these in your work

  • Replacement shown
  • HCl included
  • Atoms balanced
2 · Independent

Why might chlorination of ethane produce more than one organic product?

Give me a hint

Consider what can happen after the first substitution.

Compare my reasoning
  1. The first product still contains C–H bonds.
  2. Further substitution can replace another hydrogen.
  3. Different hydrogens in later products can lead to different substituted structures.

Further substitution can continue, producing compounds with multiple chlorine atoms and potentially different structures.

Look for these in your work

  • Remaining C–H noted
  • Further reaction described
  • Mixture possibility explained
3 · Transfer

A student writes C₂H₆ + Cl₂ → C₂H₅Cl. Identify the missing product.

Give me a hint

Count chlorine and hydrogen atoms in the equation.

Compare my reasoning
  1. The product side has one chlorine in C₂H₅Cl, but two enter as Cl₂.
  2. The displaced hydrogen also needs a product.
  3. Combine that hydrogen with the remaining chlorine atom.

HCl is missing: C₂H₆ + Cl₂ → C₂H₅Cl + HCl.

Look for these in your work

  • Atom imbalance found
  • Displaced H accounted for
  • Equation corrected

Common mistakes

  • Calling the reaction electrophilic addition
  • Omitting the hydrogen halide coproduct
  • Putting ultraviolet light in the equation as a consumed reagent
Recall without your notes

What can you explain now?

What is replaced in alkane halogenation?

Compare with the explanation

A hydrogen atom is replaced by a halogen atom

Substitution replaces an alkane hydrogen with Cl or Br.

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Make it stick

Why is ultraviolet light needed in the alkane–halogen substitution example?

If you needed the solution, close it and solve the problem again from a blank page. A correct answer is stronger when you can explain the reason for each step.

Keep learning Chemistry

Course scope and assessment

Four hundred and forty-two original lessons map the published learning outcomes across AS Chemistry Topics 1–22 and A Level Topics 23–37, with guided, independent and transfer practice and explained answers. Every numbered subject-content topic and listed outcome tag now has a mapped lesson sequence. Topic 32 maps all 12 hydroxy-compound outcome tags in 11 lessons; Topic 33 maps all 15 carboxylic-acid and derivative outcome tags in 16 lessons; Topic 34 maps all 22 nitrogen-compound outcome tags in 20 lessons; Topic 35 maps all 12 polymerisation outcome tags in 16 lessons; Topic 36 maps all four organic-synthesis outcome tags in 14 lessons; Topic 37 maps all 22 chromatography and NMR outcome tags in 18 lessons. Cambridge's 2028–2030 Version 1 syllabus states that there are no significant changes which affect teaching from the preceding edition; the routes are aligned to that edition. This is 37 of the 37 numbered subject-content topics. Full cumulative exam assessment, Paper 3 laboratory competence, Paper 5 investigation practice and human subject-teacher review remain outstanding. Written practice is self-checked and does not certify exam readiness.

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