Condensation polymerisation involves elimination reactions

Condensation polymerisation reactions lead to the formation of long polymer chains through the joining of monomers, accompanied by the elimination of small molecules such as water (H₂O).

Key features of condensation polymers:

• They are formed from reactions between monomers that contain a functional group at both ends
• These functional groups react with each other to form a covalent bond called a linkage.
• A small molecule, such as water, is eliminated each time a linkage forms between monomers.

Some common examples of condensation polymers include:

• Polyesters such as Terylene.
• Polyamides such as Nylon.
• Biological macromolecules such as proteins, carbohydrates, and DNA.

Polyesters

Polyesters are a type of condensation polymer formed from the reaction between dicarboxylic acids (or derivatives such as acyl chlorides) and diols. The carboxyl (-COOH) and hydroxyl (-OH) groups react, forming ester links in the polymer chain.

An example of a polyester is Terylene, which is synthesised from benzene-1,4-dicarboxylic acid and ethane-1,2-diol:

Polyamides

Polyamides are another type of condensation polymer, formed from dicarboxylic acids (or derivatives such as acyl chlorides) and diamines. The carboxyl and amine groups react, forming amide links within the polymer chain.

Examples of polyamides include:

• Nylon - Formed from hexanedioic acid and 1,6-diaminohexane.

• Kevlar - Formed from benzene-1,4-dicarboxylic acid and 1,4-diaminobenzene.

Polypeptides

Polypeptides are condensation polymers formed from amino acids. The carboxyl group of one amino acid reacts with the amine group of another, forming a peptide (amide) link.

Long chains of polypeptides, with more than 50 amino acid units, are called proteins. The sequence and shape of proteins are determined by the order of amino acids in their polypeptide chain.

For example, the formation of a dipeptide, where R represents the amino acid side group, is illustrated below:

Working out monomer and repeat unit structures

Drawing monomers from a polymer

To deduce the monomers that form a condensation polymer, follow these steps:

1. Identify the amide (HN-CO) or ester (CO-O) linkage between repeat units.
2. Cut the link in the middle to separate the polymer chain.
3. Add an H atom or -OH group to both ends of the molecules. H atoms are added to N or O atoms, and -OH groups to C atoms.

For example, the monomers that form a particular polyamide can be identified from its polymer structure:

Drawing repeat units from monomers

To draw the repeat unit from condensation monomers, follow these steps:

1. Place the structures of the two monomers side by side.
2. Remove an H atom from one monomer (e.g., diol or diamine) and an OH group from the other (e.g., dicarboxylic acid), forming a H₂O molecule as a by-product.
3. Connect the monomers through either an amide or ester linkage, depending on their functional groups.
4. To indicate continuity in the polymer chain, remove another H atom and OH group from the opposite ends.

The repeating unit of a polyester, for instance, can be deduced from its monomers' structures:

Comparing addition and condensation polymerisation

The mechanisms of addition and condensation polymerisation differ significantly:

Addition polymers are synthesised from alkene monomers, which contain C=C double bonds, forming chains composed solely of carbon atoms.

Condensation polymers, on the other hand, are synthesised from monomers containing functional groups such as -COOH, -NH₂, and -OH, leading to chains that incorporate ester and/or amide bonds.