Lewis Acid Catalysis
Lewis acids are used to catalyse a wide variety of reactions. The mechanism steps are:
- Lewis acid forms a polar coordinate with a basic site on the reactant (such as an O or N)
- Its electrons are drawn towards the catalyst, thus activating the reactant
- The reactant is then able to be transformed by a substitution reaction or addition reaction
- The product dissociates and catalyst is regenerated
Common Lewis acids include aluminium chloride, ferric chloride and boron trifluoride. These reactions are usually carried out in organic solvents; AlCl3, for example, reacts violently with water. Typical solvents are dichloromethane and benzene.
Read more about this topic: Lanthanide Trifluoromethanesulfonates
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