What is the simplest aromatic hydrocarbon?
Benzene (C6H6)
Why is benzene unusually stable?
It’s π electrons are delocalised over the ring, forming a conjugated system.
Why does benzene not undergo addition reactions?
Addition would break the delocalised π system and reduce stability.
What is a phenyl group?
A benzene ring with one hydrogen replaced (-C6H5)
What reactions do benzene rings undergo?
Electrophilic substitution reactions.
Why does benzene undergo substitution rather than addition?
Substitution preserves the delocalised ring, addition would destroy it.
What catalyst is used for halogenation of benzene?
What is alkylation of benzene?
Reaction with a haloalkane using AlCl3 to form an alkylbenzene.
What reagents are used for nitration of benzene?
Concentrated nitric acid and concentrated sulfuric acid.
What reagent is used for sulfonation of benzene?
Concentrated sulfuric acid.
What bonding model describes benzene?
sp2 hybridisation, σ bonds in the ring, and a delocalised π system above and below the plane.