Help your post-16 learners get to grips with how condensation polymers form and their applications

An equation for the creation of proteins from amino acids

Source: © Dan Bright

One of each original monomer joins to form the repeating unit. Each end of the repeating unit joins with another repeating unit to create another ester or amide bond between the molecules

Condensation polymers form when many monomers join together by eliminating small molecules such as water or hydrogen chloride. They can be found in nature in proteins or they can be synthesised. Examples include polyesters – such as poly(ethylene terephthalate) (PET) used in bottles – and polyamides such as Kevlar used in bulletproof vests.

Lightweight, strong and flexible, these versatile materials shape industries from fashion to engineering. Understanding their structure, synthesis and properties highlights chemistry’s role in innovation and sustainability, helping us appreciate their benefits and environmental impact.

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  • Preview of the Condensation polymerisation infographic poster on a blue background

    Infographic poster and fact sheet

    Display the poster in your classroom or on a projector. Alternatively print it and use as a handout.

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  • Preview of the Organic chemistry worksshet on a blue background

    Condensation polymerisation: knowledge check and in context worksheets

    Use these two different editable worksheets which provide a wide range of assessment questions exploring condensation polymerisation, including polyesters and the nylon rope trick experiment.

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Synthesising condensation polymers

Condensation polymers are macromolecules made from monomers which have two functional groups. The functional groups at each end of the molecule undergo a condensation reaction to form strong covalent bonds, releasing small by-products such as water. Polyesters are formed by reacting diols and dicarboxylic acids, while polyamides result from the reaction of diamines and dicarboxylic acids.

The repeating unit is formed from one of each original monomer, while each end of the repeating unit joins with another repeating unit to create another ester or amide bond between the molecules. Two molecules of water are formed during the formation of one repeating unit.

Polyamide chains also occur in proteins, through a condensation reaction between the -COOH and -NH2 group present in amino acids. This links amino acids together into a peptide chain.

Want a refresher on addition polymerisation?

Get the poster, fact sheet and classroom activity to check learners’ understanding of how addition polymers are structured and named.

Physical properties

The physical properties of condensation polymers  are shaped by strong intermolecular forcesPolyamides, such as nylon, form hydrogen bonds  between chains due to the presence of -NH and -C=O groups. This gives them strength and flexibility.

Polyesters also exhibit permanent dipole–dipole interactions, contributing to their durability. These forces explain the versatility of condensation polymers in applications ranging from clothing to engineering materials.

 All illustrations © Dan Bright 

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