Overview of the alkenes topic in chemistry.
Presented by Chris Harris from AllerTutors.com.
Designed to ensure students understand the relevant information and specifications related to alkenes.
PowerPoint materials available for purchase in the video description for further revision.
Alkenes are hydrocarbons that contain at least one carbon-carbon double bond (C=C).
General formula for alkenes: CnH2n.
Examples include ethene (C2H4) and propene (C3H6).
Unsaturation: Alkenes are unsaturated due to the presence of double bonds, unlike alkanes, which are saturated.
Reactivity: Alkenes are more reactive than alkanes due to the double bond.
They undergo addition reactions where reactants add to the carbon atoms involved in the double bond.
Addition Reactions:
Hydrogenation: Addition of hydrogen (H2) to form alkanes.
Halogenation: Reaction with halogens (e.g., Br2) to form dihaloalkanes.
Hydrohalogenation: Addition of hydrogen halides (e.g., HCl) to form haloalkanes.
Hydration: Addition of water (H2O), typically in the presence of an acid, to form alcohols.
Geometric Isomerism: Arises due to the restricted rotation around the double bond, leading to cis-trans isomers.
Structural Isomerism: Different connectivity of the carbon atoms in the molecule, leading to variations such as chain isomers.
Alkenes are used as starting materials for the synthesis of plastics, alcohols, and other chemicals.
Ethene is a key raw material in the production of polyethylene, one of the most widely used plastics.
They play a significant role in organic synthesis and the petrochemical industry.