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Question: Benzamide on treatment with \({\text{POC}}{{\text{l}}_{\text{3}}}\)gives: A. Aniline B. Benzonit...

Benzamide on treatment with POCl3{\text{POC}}{{\text{l}}_{\text{3}}}gives:
A. Aniline
B. Benzonitrile
C. Chlorobenzene
D. Benzyl amine

Explanation

Solution

In the above question, it is asked what happened when benzamide is treated with POCl3{\text{POC}}{{\text{l}}_{\text{3}}}. Since, POCl3{\text{POC}}{{\text{l}}_{\text{3}}} is a dehydrating agent, it dehydrates benzamide to form a cyanide.

Complete step-by-step answer: Phosphoryl chloride is a colourless liquid with the formula POCl3{\text{POC}}{{\text{l}}_{\text{3}}}. It hydrolyses in moist air and releases phosphoric acid and fumes of hydrogen chloride. POCl3 is a commonly used dehydrating agent in chemical laboratories. It is used as a dehydrating agent for the preparation of nitriles from primary amides.
Benzamide is a white solid with chemical formula C6H5CONH2{{\text{C}}_{\text{6}}}{{\text{H}}_{\text{5}}}{\text{CON}}{{\text{H}}_{\text{2}}}. It is the simplest amide derived from benzoic acid. It is soluble in organic solvents and water. These are organic compounds which contain a carboxamido substituent which is attached to a benzene ring. Benzamide is an extremely weak basic compound.
When benzamide reacts with POCl3{\text{POC}}{{\text{l}}_{\text{3}}}, dehydration reaction take place, which means H2O{{\text{H}}_{\text{2}}}{\text{O}} is lost from the compound which results in the formation of benzonitrile. Benzonitrile is used as an intermediate for rubber chemicals and as a solvent for nitrile rubber.
The reaction of conversion of benzamide on treatment with POCl3{\text{POC}}{{\text{l}}_{\text{3}}} to give benzonitrile is given below:

So, we can say that Benzonitrile is formed when benzamide reacts with POCl3{\text{POC}}{{\text{l}}_{\text{3}}}.

Hence, the correct option is option B.

Note: Benzo nitriles react with amine to form N-substituted benzamide after hydrolysis.
Benzo nitriles ligands are readily displaced by stronger ligands making benzo nitriles complexes useful synthetic intermediates.
Nitrile-hydrolysing enzymes were generally unstable for commercial use in the isolated or purified state.