The reaction is driven by the breaking of the -bond within the double bond of the monomer. This bond is weaker than the -bond and is susceptible to chemical attack.
Once the -bond breaks, each carbon atom involved in the original double bond has an available electron to form a new -bond with an adjacent monomer.
This process converts an unsaturated starting material (alkene) into a saturated long-chain molecule (alkane-like backbone), resulting in a significant change in physical properties such as density and melting point.
To identify the repeat unit from a monomer, first draw the monomer in a 'H' shape with the bond in the center and all substituents pointing vertically up or down.
Change the double bond to a single bond and extend two horizontal 'continuation bonds' out from each carbon atom through a set of square brackets.
Place the subscript outside the bottom right of the brackets to indicate that the unit repeats many times. The chemical formula of the repeat unit must match the chemical formula of the monomer.
To find the monomer from a polymer section, identify the simplest repeating two-carbon segment, remove the continuation bonds, and restore the double bond.
| Feature | Monomer | Repeat Unit |
|---|---|---|
| Bonding | Contains double bond | Contains single bond |
| Saturation | Unsaturated | Saturated |
| Representation | Individual molecule ( molecules) | Shown in brackets with continuation bonds |
| Naming | e.g., Ethene | e.g., Poly(ethene) |