Nylon and polyester are made another way. Each monomer has a functional group at both ends, and two different monomers take turns along the chain.
You have already met condensation: two molecules join and give off a small molecule, usually water. A condensation polymer forms when this happens at every link in the chain, so one water molecule is given off for every link.
Nylon: amine meets acid
Nylon-6,6 is made from two monomers. Hexane-1,6-diamine is a chain of 6 carbons with an amine group, -NH₂, at each end. Hexanedioic acid is a chain of 6 carbons with a carboxylic acid group, -COOH, at each end. You have met both groups before. The two 6s in the name count the carbons in each monomer.
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When an acid end meets an amine end, the -OH from the acid and one H from the amine leave together as a water molecule. The carbon and the nitrogen bond to each other, making an amide link, -CONH-.
Each monomer has two ends, so it joins on both sides: diamine, acid, diamine, acid, thousands of times over. Your body uses the same link to join amino acids into proteins, where it is called a peptide bond, as the next lesson shows.
Polyester: alcohol meets acid
A polyester joins its monomers with the familiar ester link. One monomer is a diol, an alcohol with an -OH group at each end, such as ethane-1,2-diol. The other is an acid with a -COOH group at each end. Each -OH meets a -COOH, water is given off, and an ester link, -COO-, joins them.
The best-known polyester is PET, made from ethane-1,2-diol and benzene-1,4-dicarboxylic acid, whose two -COOH groups sit on opposite corners of a benzene ring. PET makes plastic drinks bottles, and spun into fibres it makes the polyester in many clothes.