
Consider the above reactions, the product A and product B, respectively are




The question provides two chemical reactions, and we need to identify products A and B.
**Reaction 1: Formation of Product A**
The first reaction involves converting the amide to a product using KOBr (Potassium hypobromite). This is a classic example of the Hofmann rearrangement, where an amide is converted into an amine with the loss of one carbon atom.
The intermediate is an isocyanate, which hydrolyzes to give a primary amine.
Therefore, product A is a primary amine corresponding to the aromatic group.
**Reaction 2: Formation of Product B**
In the second reaction, LiAlH_4 followed by hydrolysis is used. Lithium aluminium hydride is a strong reducing agent that reduces amides to amines.
This reaction preserves the number of carbon atoms, converting the amide carbonyl group to a methylene group.
Therefore, product B is the respective amine without carbon atom loss.
**Conclusion:**
The products are determined as follows:
The correct answer, considering the reactions provided, is: