Reactions of Alkenes (Edexcel International A Level Chemistry)

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Alkenes - Reactions

  • The double bond in alkenes is an area of high electron density (there are four electrons found in this double bond)
  • This makes the double bond susceptible to attack by electrophiles (electron-loving species)
  • An electrophilic addition is the addition of an electrophile to a double bond
  • The C-C double bond is broken, and a new single bond is formed from each of the two carbon atoms
  • Electrophilic addition reactions include the addition of:
    • Hydrogen (also known as hydrogenation reaction)
    • Steam (H2O (g))
    • Hydrogen halide (HX)
    • Halogen

Hydrocarbons Electrophilic Addition Reactions, downloadable AS & A Level Chemistry revision notes

The diagram shows an overview of the different electrophilic addition reactions alkenes can undergo

Oxidation

  • Alkenes can also be oxidised by acidified potassium manganate(VII) (KMnO4) which is a very powerful oxidising agent
  • When shaken with cold dilute KMnO4 the pale purple solution turns colourless and the product is a diol
    • This colour change means this reaction can be used, like bromine, to distinguish alkanes from alkenes (alkanes do not have double bonds and so are not oxidised in this way)

screenshot-2022-03-14-133409

  • Although you do not need to know the full details of the working of this reaction you can think of it as an oxidation followed by an addition
    • The potassium manganate provides an oxygen atom (oxidation) 
    • Then water in the solution provides another oxygen atom and two hydrogen atoms, so there is addition of two OH groups across the double bond

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Sonny

Author: Sonny

Expertise: Chemistry

Sonny graduated from Imperial College London with a first-class degree in Biomedical Engineering. Turning from engineering to education, he has now been a science tutor working in the UK for several years. Sonny enjoys sharing his passion for science and producing engaging educational materials that help students reach their goals.