Question:
The final product C, obtained in this reaction, would be:
The final product C, obtained in this reaction, would be:
Updated On: Apr 27, 2026
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The Correct Option is C
Solution and Explanation
In order to obtain a monobromo compound, the amino group is first subjected to acetylation prior to the bromination step. Following the bromination, bromoacetanilide is then subjected to acid hydrolysis, resulting in the production of the desired halogenated amine.
So, the correct option is (C).
So, the correct option is (C).
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Concepts Used:
Preparation of Haloarenes
- Preparation by Electrophilic Substitution Reaction: Electrophilic Substitution helps in the preparation of Haloarenes like aryl bromides and aryl chlorides by using the halogens such as chlorine and bromine in the presence of Lewis Acid. But for this reaction to be fruitful, it is compulsory that the reaction takes place in the presence of Lewis Acid and must be carried out in dark.
- Preparation by Sandmeyer’s Reaction: In this case, in order to form diazonium salt in the presence of cold mineral water, the primary aromatic amine has to react with sodium nitrate. Here, the reaction of sodium nitrate with HX will prepare HNO2 at a temperature of 273-278 K.
Read More: Haloalkanes and Haloarenes