|  | Chapter 11 : Arenes and Aromaticity |  | 
  
Reactions of the Benzylic position 
Functional groups in a benzylic position are generally more reactive than the 
  related isolated functional group. 
  - Benzylic C-H can easily be radically halogenated since the benzylic radical is 
    resonance stabilised.
- Benzylic C-H bonds of alkyl benzenes can be oxidised 
    to give benzoic acids
- Benzylic halides readily undergo nucleophilic substitution reactions even with weak nucleophiles.
- Benzylic halides or alcohols readily eliminate to give conjugated alkenes.
- Alkenylbenznes undergo addition reactions to give typical addition products.
These reactions are summarised in the following table: