Reactivity 3.4 – Electron-pair sharing reactions

R3.4.5 – Electrophilic addition of alkenes

  • Alkenes are unsaturated hydrocarbons with a C=C double bond
  • The double bond is electron dense which enables it to undergo reactions with electrophiles
  • The pi bond in the double bond is selectively broken to form two new single bonds. This enables addition reactions
  • Addition reactions only have a single product
  • Adding water across the double bond in an alkene is known as hydration
  • Highly concentrated sulphuric acid is used as a catalyst for this reaction due to water’s weak properties as an electrophile
  • The product of hydration of an alkene is an alcohol with the same number of carbons (eg. ethene becomes ethanol)
  • Addition of halogens produces dihalogeno compounds
  • The pi bond breaks and forms two new single bonds which each bond to one halogen atom
  • Addition of hydrogen halides produces halogenoalkanes
  • All hydrogen halides can undergo addition reactions with alkenes but the order of the halogens varies
  • HI reacts most readily followed by HBr then HCl