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What is Aromatic Nuclophilic Substitution Reactions about?

Aromatic nucleophilic substitution reactions require high activation energy and are generally slow, but can be facilitated by strong electron withdrawing groups (EWGs). The reactivity of halides increases with more EWGs, and different mechanisms such as SN1Ar and SRN (Sandmeyer) reactions can occur, particularly with diazonium salts. The formation of benzyne intermediates also plays a crucial role in these reactions, leading to various substitution products depending on the substituents present.

Author

deepikamurugadosslakshmi

Language

EN