Question

which shows nucleophilic aromatic substitution Rxn a (Aniline) b (phenois) c (benzene) d (nitro benzene)​

Answer 1

(Aniline)

The attacking species (CH3O–) is the nucleophile, and the ring is the electrophile. Since the nucleophile is the attacking species, this type of reaction has come to be known as nucleophilic aromatic substitution.

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Answer 2

Answer:

The extra stability means that benzene will less readily undergo addition reactions. The more loosely held electrons are open to attack by electrophiles. Hence, the characteristic reaction of benzene is electrophilic substitution

2.Lewis Acids Accelerate The Rate of Electrophilic Aromatic Substitution Reactions. The reaction of Cl2 with benzene is faster than toenail growth, but not by much [ref] (It is, however, much faster with more electron-rich aromatics such as toluene and phenol).