Hydrocarbons: Alkenes Summary
Hydrocarbons: Alkenes
Alkenes are hydrocarbons containing one or more C=C bonds.
They can form long-chain molecules such as polythene and polystyrene.
Polyunsaturated fats and oils contain multiple C=C bonds, essential in diet.
Structure and Properties
Alkenes are a homologous series with the general formula CnH{2n}.
Examples: Ethene (C2H4), Propene (C3H6), But-1-ene, But-2-ene (C4H8).
Alkenes possess no permanent dipole; they exhibit van der Waals forces.
Lighter alkenes are gases; heavier alkenes are solids due to increased van der Waals forces.
Structural Isomers
Isomers like but-1-ene and but-2-ene differ in the position of the C=C bond.
Naming follows IUPAC rules; requires numbering based on the lowest C=C bond position.
Example naming: Pent-1-ene and Pent-2-ene based on carbon chain.
C=C Functional Group
C=C contains a sigma (σ) bond and a pi (π) bond formed from p-orbital overlap.
π-bond is weaker than σ-bond, making alkenes more reactive than alkanes.
Geometric isomers exist due to restricted rotation around C=C bonds.
Geometric Isomers
Designated as cis-trans or E-Z based on arrangements of groups around C=C bond.
cis: Similar groups on the same side; trans: on opposite sides.
E-Z notation used when complex groups are present.
Reactions of Alkenes
Alkenes participate in addition reactions with hydrogen, halogens, and hydrogen halides.
Hydrogenation involves adding H2 across the C=C bond creates alkanes.
For example: Propene + H2 yields propane.
Halogenation forms halogenated alkanes, testing C=C presence by decolorizing bromine water.
Electrophilic addition using HBr follows Markovnikov's Rule, favoring stable carbocation formation.
Polymerization
Polyethene forms from the polymerization of ethene (addition reaction of monomers).
Similar process applies for other alkenes to form polypropene, polyvinylchloride, etc.
Addition polymerization is characterized by forming larger molecules from alkenes sharing double bonds.