The ethylation reaction of benzene involves the addition of an ethyl group on the benzene ring. Such a reaction is called a Friedel-Craft alkylation reaction. This reaction takes place in the presence of a Lewis acid.
Any Lewis acid like anhydrous FeCl3, SnCl4, BF3 etc. can be used during the ethylation of benzene.
Give plausible explanation for:
(a) Diazonium salts of aromatic amines are stable.
(b) Aniline does not undergo Friedel-Crafts reaction.
(c) Aniline on nitration gives substantial meta product.
Aromatic hydrocarbons, sometimes known as arenes, are aromatic organic molecules made up entirely of carbon and hydrogen. In aromatic compounds a benzene ring which is named after the simple aromatic chemical benzene, or a phenyl group when part of a larger structure, is the configuration of six carbon atoms.
Read More: Aromaticity
This reaction involves the replacement of one substituent on the ring of an aromatic hydrocarbon, commonly a hydrogen atom, by a different substituent group.
The common types of aromatic substitution reactions are:
In these types of reactions, the coupling of two fragments that have a radical nature is achieved with the help of a metal catalyst