Alkenes and Cracking
Cracking breaks long-chain alkanes into shorter, more useful alkanes and alkenes (and sometimes hydrogen), using heat and a catalyst. It matches supply to demand: there's more long-chain oil than needed, and not enough petrol. Alkenes () contain a C=C double bond, so they undergo addition reactions: with bromine, hydrogen (→ alkanes) and steam (→ alcohols). Bromine water turns from orange to colourless with an alkene but not with an alkane.
Learning objectives
- Describe cracking and explain why it is needed.
- Write cracking equations.
- Describe addition reactions of alkenes.
- Use bromine water to distinguish alkanes and alkenes.
A refinery produces lots of heavy fuel oil but customers want petrol. What can it do?
Core idea
Refineries have far more heavy oil than anyone wants, and not enough petrol. Cracking snaps big molecules into smaller, more valuable ones, and produces alkenes, the raw material for plastics.
Cracking makes short alkanes and alkenes. The C=C bond in alkenes opens up so other atoms can add across it.
1. Cracking
- Goal
- Missing product.
- Strategy
- Conserve C and H.
- Carbons left.
- Hydrogens left.
2. Addition reactions
The double bond opens; nothing else is produced.
Why is "addition" a good name for these reactions?
Summary
- Cracking: heat + catalyst.
- Alkenes: C=C, addition.
- Bromine water decolourised.
- Cracking
- Breaking long-chain hydrocarbons into shorter ones.
- Unsaturated
- Containing a C=C double bond.
- Addition reaction
- Two molecules join to form one product.
Create a free account to read the rest of this lesson: key formulae, worked examples, explore the graph, common mistakes, exam tip, guided practice and more. Your answers are checked and your progress is saved.