MHT CET202519 Apr 2025Evening ShiftChemistryAldehydes and KetonesActual
Benzonitrile on reduction with stannous chloride in presence of hydrochloric acid followed by acid hydrolysis forms,
Options
- ABenzal chloride
- BBenzoyl chloride
- CBenzophenone
- DBenzaldehyde
Correct answer
D. Benzaldehyde
Step-by-step solution
The Stephen reaction reduces benzonitrile to benzaldehyde through an imine hydrochloride intermediate. Stannous chloride and hydrochloric acid reduce C₆ H₅CN to the imine hydrochloride: C₆ H₅CN + SnCl₂ + 2HCl C₆ H₅CH=NH HCl + SnCl₄ . Acid hydrolysis yields the aldehyde: C₆ H₅CH=NH HCl + H₂ O [H^+] C₆ H₅CHO + NH4Cl . The product is benzaldehyde, corresponding to option D .