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 |