HomeChemistryC4: Organic ChemistryC4.5 Addition Polymers

C4: Organic Chemistry

C4.1 Introduction to Organic ChemistryC4.2 Crude Oil and Fractional DistillationC4.3 Burning Hydrocarbons – Complete and Incomplete CombustionC4.4 Alkanes and AlkenesC4.5 Addition Polymers
C4: Organic Chemistry

Addition Polymers

Understand how alkenes join to form long polymer chains and their environmental impact

Polymer materials

Polymers Everywhere

From monomers to everyday plastics

What are Polymers?
Long chains from small molecules

Polymers are long-chain molecules made of many repeating units called monomers. In addition polymerisation, many alkene molecules join together by opening their C=C double bonds. No atoms are lost in this process – the monomer formula equals the repeating unit formula.

The process works because alkenes are unsaturated. When the double bond opens, each carbon can form a new bond with the carbon of an adjacent monomer, creating a long chain. Thousands or millions of monomers can join in this way.

Key Exam Point

To draw a polymer from its monomer: remove the double bond, add single bonds on each side, and put brackets around the unit with subscript 'n'. Example: CH₂=CH₂ becomes ( -CH₂-CH₂- )ₙ

Common Addition Polymers
Polymers and their uses

Poly(ethene) is made from ethene (C₂H₄). It exists as LDPE (low-density, flexible – plastic bags) and HDPE (high-density, rigid – bottles, containers). The difference is in how the chains are arranged.

Poly(propene) is made from propene (C₃H₆). It's stronger than poly(ethene) and is used for car bumpers, packaging, and rope.

Poly(chloroethene) or PVC is made from chloroethene (C₂H₃Cl). It's used for pipes, flooring, and window frames. It's strong, rigid, and resistant to chemicals.

Addition Polymer Builder
Watch monomers join to form long polymer chains

Monomer: Ethene

C₂H₄Contains C=C double bond
CC

Double bond ready to open

Polymer: Poly(ethene)

( -CH₂-CH₂- )ₙ

Uses: Plastic bags, bottles (LDPE/HDPE)

Monomers Ready

CCCCCCCC

Double bonds shown between carbon atoms

Note: Addition polymers are non-biodegradable. They persist in the environment for hundreds of years. Recycling involves melting and reshaping, or chemical breakdown to monomers.

Environmental Issues
The problem with plastics

Addition polymers are non-biodegradable – microorganisms cannot break them down. They persist in the environment for hundreds of years, accumulating in landfills and oceans.

Burning polymers releases energy but can produce toxic fumes, especially if the polymer contains halogens (like PVC, which releases hydrogen chloride gas).

Recycling helps reduce waste. Mechanical recycling involves melting and reshaping polymers. Chemical recycling breaks polymers back into monomers that can be used to make new polymers.

Key Terms Flashcards
Click the card to reveal the definition

Polymer

A long-chain molecule made of many repeating units (monomers) joined together

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Worked Example
Drawing polymer structures

Question:

Draw the repeating unit for poly(propene) from the monomer propene (CH₂=CH-CH₃) and explain why it is non-biodegradable.

Answer:

Monomer: CH₂=CH-CH₃ (propene)

Repeating unit:

( -CH₂-CH(CH₃)- )ₙ

The C=C double bond opens, and each carbon forms a bond to the adjacent monomer. The CH₃ group remains attached to one carbon.

Why non-biodegradable: The C-C bonds in the polymer backbone are very strong and unreactive. Microorganisms do not have enzymes capable of breaking these bonds, so the polymer cannot be decomposed naturally.

Test Your Knowledge
Question 1 of 6

What is a polymer?