Polymerisation Reactions
A concise revision guide to addition polymerisation, how alkene monomers form poly(alkenes), how to recognise repeating units and why poly(ethene) and poly(propene) have useful material properties.
What Is Addition Polymerisation?
Addition polymerisation is a chain-forming reaction in which many alkene molecules join together to form a long-chain polymer.
The alkene molecules are the monomers. During polymerisation, the carbon-carbon double bonds open up, allowing the monomers to connect into a long saturated carbon chain.
No small molecule is eliminated during addition polymerisation, so there are no by-products.
Key idea: Addition polymers form when many alkene monomers join together by opening their C=C double bonds.
From Ethene to Poly(ethene)
Ethene, CH2=CH2, is an alkene monomer. When many ethene molecules polymerise, the C=C double bond in each monomer opens and the carbon atoms form new C-C single bonds to neighbouring monomers.
The polymer formed is poly(ethene). The repeat unit is written in brackets, with an n outside the brackets to show that the unit is repeated many times.
Equation focus: Include n before the monomer and n after the bracketed repeating unit when writing addition polymerisation equations.
The C=C bond in ethene changes into single bonds in the polymer chain, giving a bracketed repeating unit.
Recognising Repeating Units
A repeating unit is the smallest section of the polymer chain that repeats over and over again.
To recognise the repeating unit in a poly(alkene), look for the section of the carbon chain that came from one alkene monomer. The double bond is no longer present in the polymer because it has opened during the addition reaction.
The brackets should cut through single bonds at both ends of the repeating unit. This shows that the chain continues on both sides.
Repeating unit: The section of a polymer chain that is repeated many times to form the polymer.
The bracketed section identifies one repeat of the polymer chain and the open bonds show that the chain continues.
From Propene to Poly(propene)
Propene can also undergo addition polymerisation. Each propene monomer opens its C=C double bond and links to other monomers to form poly(propene).
The CH3 group from propene remains attached to every other carbon in the polymer repeat unit. This side group helps make poly(propene) stiffer than poly(ethene).
Exam focus: When converting a monomer into a repeat unit, keep every substituent attached to the same carbon. Only the C=C bond changes into C-C single bonds.
The CH3 side group remains part of the repeat unit when propene forms poly(propene).
Properties and Uses of Poly(alkenes)
Different poly(alkenes) have different physical properties because their repeat units and side groups are different.
Poly(ethene) is widely used for plastic bags, buckets and bottles. It is useful because it is flexible, easy to mould, waterproof, chemically resistant and has low density.
Poly(propene) forms a stiffer polymer, so it is suitable for products that need greater strength and rigidity. It is commonly used in utensils, storage containers, fibres, ropes and carpets.
| Polymer | Useful properties | Common uses |
|---|---|---|
| Poly(ethene) | Flexible, easy to mould, waterproof, chemically resistant and low density. | Plastic bags, buckets and bottles. |
| Poly(propene) | Stiffer, stronger and more rigid than many simple flexible plastics. | Utensils, storage containers, fibres, ropes and carpets. |
Common Exam Mistakes
- Do not draw a C=C double bond inside the polymer repeat unit. The double bond opens during addition polymerisation.
- Do not forget the n before the monomer and after the bracketed repeat unit in a polymerisation equation.
- Do not remove side groups such as CH3 when converting propene into poly(propene).
- Do not describe addition polymerisation as forming a small molecule by-product.
Check Your Understanding
Use these short activities to check addition polymerisation, repeating units and the uses of poly(alkenes).
Master Alkenes for Edexcel A Level Chemistry
Continue from these free revision notes into the full Topic 6C Alkenes course, with guided video teaching, diagnostic MCQ practice, teacher-marked short-answer questions and a specification assignment with a personalised progress report.
Guided video teaching
Learn the chemistry and exam technique through structured video lessons with worked examples and walkthroughs.
Instant MCQ feedback
Auto-marked MCQ quizzes provide immediate diagnostic feedback for every answer choice.
Teacher-marked SAQs
Submit written exam responses and receive chemistry specialist feedback with improvement guidance.
Progress tracking
Identify strengths and weaknesses across the full Topic 6C specification with targeted reporting.
See how the course works
Click play to start the course preview animation.
Some ionic radii are shown.
| Ion | Ionic radius / nm |
|---|---|
| Na+ | 0.102 |
| K+ | 0.138 |
| F− | 0.133 |
| Cl− | 0.180 |
Which compound has the strongest ionic bonding?
Explain why the metallic bonding in magnesium is much stronger than that in sodium.
Copyright notice: This OLS revision content, including the explanations, layout, diagrams, tables and embedded learning structure, is authored for Online Learning System by Dr. Mohammed Al-Fatah. It may not be copied, reproduced, redistributed or adapted without written permission.