Step 1: Understanding Hoffmann’s bromamide degradation reaction.
Hoffmann’s bromamide degradation reaction involves the reaction of an amide with bromine in the presence of a strong base (usually NaOH). The reaction results in the removal of the acyl group from the amide, forming a primary amine with one less carbon atom.
Step 2: Analyzing the Statements.
- (a) Alkyl amides do not react: This statement is incorrect. Alkyl amides can react in Hoffmann’s bromamide degradation, as long as they are primary amides.
- (b) Secondary amides do not form secondary amides: This statement is correct. Secondary amides do not undergo the same reaction as primary amides in the Hoffmann degradation because they lack the required functional group for the degradation.
- (c) Ratio of NaOH and Br₂ is 4 : 2: This is incorrect. The typical ratio of NaOH to Br₂ used in the Hoffmann degradation reaction is 4 : 1, not 4 : 2.
- (d) Na₂CO₃, NaBr and H₂O also formed along with amine: This is correct. Along with the formation of the primary amine, the reaction also produces sodium carbonate (Na₂CO₃), sodium bromide (NaBr), and water (H₂O).
Step 3: Conclusion.
The correct answer is (C), as statements (b) and (d) are accurate.
Final Answer: b and d only