Alkenes are unsaturated hydrocarbons General formula is CnH2n Alkenes contain a carbon- carbon double bond somewhere in their structure C C H H H H Ethene C C H H H C H H H Propene Numbers need to be added to the name when positional isomers can occur C H H C C C H H H H H H But-1-ene But-2-ene C=C double covalent bond consists of one sigma (σ) bond and one pi (π) bond. π bonds are exposed and have high electron density. They are therefore vulnerable to attack by species which ‘like’ electrons: these species are called electrophiles. C C C C H H H H H H H H N Goalby chemrevise.org 1 The π bond is formed by sideways overlap of two p orbitals on each carbon atom forming a π-bond above and below the plane of molecule. The π bond is weaker than the σ bond. p orbitals C-C sigma bond C-C pi bond C-C sigma bond C-C pi bond The arrangement of bonds around the >C=C< is planar and has the bond angle 120o Formation of π bond C C H H H H
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4.1.3 Alkenes
Properties of alkenes (a) alkenes as unsaturated hydrocarbons containing a C=C bond comprising a π-bond (sideways overlap of adjacent p-orbitals above and below the bonding C atoms) and a σ-bond (overlap of orbitals directly between the bonding atoms) (see also 4.1.2 a); restricted rotation of the π-bond Hybridisation is not required. HSW1 Use of model of orbital overlap to explain covalent bonding in organic compounds. (b) explanation of the trigonal planar shape and bond angle around each carbon in the C=C of alkenes in terms of electron pair repulsion (see also 2.2.2 g–h, 4.1.2 b) M4.1, M4.2