Step 1: 1-Chloro-2,4,6-trinitrobenzene undergoes hydrolysis when warmed with water or aqueous NaOH due to the presence of the electrophilic chlorine atom attached to an aromatic ring. The reaction involves nucleophilic substitution.
Step 2:
- (B) Chloroform does not undergo hydrolysis under normal conditions.
- (C) Bromoethane undergoes nucleophilic substitution, but hydrolysis is not a typical reaction.
- (D) Iodoform undergoes reaction with alkali to give a precipitate, but it is not typically hydrolyzed in the presence of water or NaOH.
Conclusion: 1-chloro-2,4,6-trinitrobenzene undergoes hydrolysis.