The fundamental mechanism involves the breaking of the -bond in the double bond of the monomer.
Each carbon atom in the former double bond now has an available electron to form a new -bond with a carbon atom from an adjacent monomer molecule.
This process continues in a chain reaction, effectively 'opening up' the double bonds to create a continuous backbone of single-bonded carbon atoms.
Because no atoms are gained or lost, the empirical formula of the polymer is identical to that of the monomer, though its physical properties (like melting point and density) differ significantly.
| Feature | Monomer | Polymer |
|---|---|---|
| Bonding | Contains double bond (Unsaturated) | Contains single bonds (Saturated) |
| State | Often gas or liquid at room temperature | Usually a solid plastic or resin |
| Reactivity | Highly reactive due to the double bond | Generally chemically inert and stable |
| Naming | Based on IUPAC alkene rules (e.g., Ethene) | Prefix 'poly' + monomer name (e.g., Polyethene) |
The 'n' Rule: Always include the '' in the equation. On the left side, it is a coefficient ( Monomer); on the right side, it is a subscript (Polymer).
Bond Alignment: Ensure that the groups attached to the carbons in the monomer remain attached to the same carbons in the polymer. Do not rearrange side groups during the process.
Trailing Bonds: In diagrams, trailing bonds must clearly extend through the brackets to show that the chain continues; stopping them inside the brackets is a common error that loses marks.
Verification: Check that the number of atoms of each element is the same on both sides of the reaction equation to confirm mass conservation.