Condensation polymers form when a water molecule is removed from the species of a reaction. Polyesters and polyamides can be formed in this way.
When making a polyester, monomers are joined together by ester linkages in a long chain to form the polymer.
Polyesters made from one monomer containing two different functional groups:
a hydroxyl group (-OH)
a carboxyl group (-COOH)
Polyesters made from 2 monomers each containing two functional groups
one monomer is a diol, with two hydroxyl groups
one monomer is a dicarboxylic acid, with two hydroxyl groups
During a condensation reaction between two monomers a hydroxyl group on the diol reacts with a carboxyl group on the dicarboxylic acid forming an ester linkage and water.
A polyester can also be made using an diacyl chloride instead of a dicarboxylic acid. With an diacyl chloride, hydrogen chloride is lost, instead of water.
Polyamides are condensation polymers formed when monomers are joined together by amide linkages in a long chain to form the polymer.
Polyamides can be made from one monomer containing both a carboxylic acid (or acyl chloride) and an amine group - or from two monomers, one containing two carboxylic acid groups (or acyl chlorides) and the other containing two amine groups.
A polypeptide or protein contains many different aminoacids all linked together by amide bonds.
When an amide bond is formed water is lost.
Amino acids undergo condensation polymerisation to form polypeptides or proteins
-CONH- is the amide linkage
-COO- is an ester linkage
Polyesters and polyamides can be hydrolysed using hot aqueous alkali such as sodium hydroxide or by hot aqueous acid such as hydrochloric acid.
addition polymerisation
Monomer contains a C—C double bond
Backbone of polymer is a continuous chain of carbon atoms