57. Addition Reactions of Alkenes

1. Why Addition Reactions Occur

Alkenes are unsaturated hydrocarbons, meaning they contain at least one carbon-carbon double bond (C=C). This double bond serves as the functional group. Because it can break and "open up," alkenes can add other molecules to their structure, a process called an addition reaction.

2. Reaction with Hydrogen (Hydrogenation)
  • Conditions: Requires the presence of a catalyst.

  • Process: The double bond breaks, and hydrogen atoms bond to the remaining spots on the carbon atoms.

  • Product: The alkene is converted into a saturated alkane.

  • Example: Propene + Hydrogen → Propane

3. Reaction with Water (Hydration)
  • Conditions: Requires a catalyst and high temperatures (so that water is in the form of steam).

  • Process: The water molecule (H2O) splits into a hydrogen atom (H) and an OH group, which both bond to the carbon atoms.

  • Product: An alcohol.

  • Example: Ethene + Water → Ethanol

  • Separation: After the reaction, unreacted ethene is removed by cooling the mixture (it stays as a gas). The remaining water and ethanol are then separated using fractional distillation.

4. Reaction with Halogens
  • Conditions: No catalyst is required; it simply involves mixing/shaking the reactants.

  • Process: Halogen atoms (like Bromine, Chlorine, or Iodine) add across the double bond.

  • Example: Ethene + Bromine → Dibromoethane

5. Testing for Alkenes

The reaction with bromine is the standard test to distinguish alkenes from alkanes:

  • Alkenes: Being reactive and unsaturated, they react with orange bromine water and decolorize it (turning it from orange to colorless).

  • Alkanes: Being saturated, they do not react with bromine water, so the solution remains orange.

Summary of Addition Reactions

Reactant

Product

Class of Product

Hydrogen (H2)

Alkane

Saturated Hydrocarbon

Water (H2O)

Alcohol

Organic Compound (-OH)

Halogens (e.g., Br2)

Haloalkane

Halogenated Hydrocarbon