Cambridge IGCSE · Topic 11.8
IGCSE Chemistry 0620 / Topic 11 / IGCSE

Thousands of alkenes, one chain.

Open the C=C double bond of ethene and the molecules link into long chains of poly(ethene), the plastic in bags and bottles. Learn to draw the repeat unit, work backwards to the monomer, and weigh up what happens to plastics when we throw them away.

The key idea

Polymers are large molecules built up from many small molecules called monomers. Many plastics are polymers made from chemicals obtained from crude oil. In addition polymerisation, alkene monomers join when their C=C double bonds open; the polymer is the only product. Ethene forms poly(ethene), whose repeat unit is –CH2–CH2–. Extended: draw the polymer from a given alkene, and deduce the monomer from a section of polymer. Plastics are hard to dispose of: they are non-biodegradable and fill landfill sites, they accumulate in oceans, and burning them can release toxic gases. Recycling reduces these problems.

n CC HHHH CC HHHH n ethene (monomer)poly(ethene), repeat unit addition polymerisation each C=C opens and the monomers join into one long chain the polymer is the only product
Fig. 1: addition polymerisation of ethene and the repeat unit of poly(ethene)
Section 01

Monomer to polymer.

Add reagents across the double bond of an alkene in the simulator, then link many alkene molecules together to make a polymer.

Stage 1 · Learn

Check what the sim just showed you

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What is a polymer?

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Which monomer is used to make poly(ethene)?

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Why can alkenes form addition polymers but alkanes cannot?

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Why do plastics cause problems in landfill sites?

Section 02

Polymer to monomer.

Extended. Every addition polymer has a two-carbon backbone repeat unit. Find it, then put the double bond back.

MonomerPolymerRepeat unitUse
ethene, CH2=CH2poly(ethene)–CH2–CH2–bags, bottles
propene, CH2=CHCH3poly(propene)–CH2–CH(CH3)–crates, ropes
chloroethene, CH2=CHClpoly(chloroethene), PVC–CH2–CHCl–pipes, window frames
tetrafluoroethene, CF2=CF2PTFE–CF2–CF2–non-stick coatings

Method: take any two adjacent backbone carbons with their side groups, remove the continuation bonds and draw a C=C double bond between them. The CH3 in poly(propene) is a side group, not part of the backbone.

Section 03

The problem with plastics.

Plastics are useful because they are unreactive and durable. Those same properties make them hard to get rid of.

DisposalProblem
landfillnon-biodegradable, so they last for hundreds of years and landfill space runs out
oceansplastic waste accumulates; animals swallow it or become trapped; it breaks into microplastics
burningreleases carbon dioxide (a greenhouse gas); PVC and others release toxic gases such as hydrogen chloride; incomplete combustion gives carbon monoxide
recyclingsaves crude oil and reduces waste, but plastics must be collected and sorted by type
Examiner trap

The repeat unit has single bonds only: the double bond belongs to the monomer, not the polymer. Do not include the side group in the backbone (poly(propene) has a two-carbon repeat unit with a CH3 branch, not three carbons in a row). Plastics are made from crude oil, so they are not renewable; "non-biodegradable" means microorganisms cannot break them down.

Stage 2 · Exam

Exam-style questions

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(Extended) The repeat unit of a polymer is –CH2–CHCl–. What is the monomer?

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(Extended) What is the repeat unit of poly(propene)?

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Which gas is a toxic product of burning PVC, poly(chloroethene)?

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A sample of poly(ethene) has Mr 56 000. How many ethene monomers joined to make one molecule?

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Addition polymers, mastered.

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Six original Cambridge-style questions
Monomers, addition polymerisation, repeat units, deducing monomers, and the disposal problems of plastics.