Ethene is an alkene produced by the cracking of crude oil fractions. Ethene can be used as a monomer to produce poly(ethene). Explain how the structure of ethene allows it to undergo addition polymerisation to form a long chain polymer.
Written & reviewed by James Millett — Biology (Imperial College London), PGCE Science (University of Cambridge).
Poly(ethene) is one of the most widely used plastics in the world. It is produced from ethene, a small molecule obtained from cracking crude oil fractions.
Model answer (4 marks)
Ethene contains a C=C double bond, which is an unsaturated site.
The double bond opens during the addition reaction, breaking the C=C bond.
The opened bonds react with other ethene molecules, linking them together.
No small molecules are produced; the reaction gives only the long‑chain polymer.
The double bond opens during the addition reaction, breaking the C=C bond.
The opened bonds react with other ethene molecules, linking them together.
No small molecules are produced; the reaction gives only the long‑chain polymer.
Examiner tips
- Mention the C=C double bond and its unsaturation first. Explain that the double bond breaks and the radicals add. Show that all monomers join, giving a single polymer chain. State that no by‑products are formed in addition polymerisation.
Common mistakes
- Forgetting to mention the double bond. Saying the reaction produces small molecules. Using vague terms like "reacts" without describing the opening of the double bond.
Mark scheme (4 marks)
- Ethene contains a carbon–carbon double bond, making it unsaturated
- The double bond opens / breaks during the reaction
- Many ethene monomers join together to form a long chain
- No other molecules / small molecules are produced in addition polymerisation (no by-products lost)
Key terms in this question
addition polymerisation · monomer · alkene · long chain polymer
Related
- All OCR GCSE Chemistry A: Gateway Science (J248) revision notes →
- How to answer a "Explain" question →
- Decode the mark scheme abbreviations →
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