p-chloronitrobenzene undergoes nucleophilic substitution faster than chlorobenzene. Give reason.

p-Chloronitrobenzene undergoes nulceophilic substitution faster than chlorobenzene. Explain giving the resonating structures as well.

(A) 4-Nitrochlorobenzene undergoes nucleophilic substitution more readily than chlorobenzene. (R) Chlorobenzene undergoes nucleophilic while 4-nitro chlorobenzene undergoes nucleophilic substitution by addition elimination mechanism.

Phenol undergoes aromatic substitution to give

Which of the following undergoes electrophilic substitution reactions faster than benzene?

Assertion: tert-butylbromide undergoes S_(N)1 nucleophilic substitution readily than n-butyl bromide. Reason: It proceeds by the formation of stable carbocation.

Assertion: tert-butylbromide undergoes S_(N)1 nucleophilic substitution readily than n-butyl bromide. Reason: It proceeds by the formation of stable carbocation.

Phenol does not undergo nucleophilic substitution reaction easily due to: