The products formed when Aniline reacts with water, and will be, respectively:
1. | p-Bromoaniline; p-Chloroaniline |
2. | 2,4,6-Tribromoaniline; p-Chloroaniline |
3. | 2,4,6-Tribromoaniline; Benzenediazoniumchloride |
4. | p-Bromoaniline; Benzenediazoniumchloride |
The reaction which gives isocyanide is:
1. Reimer Tiemann reaction.
2. Carbylamine reaction.
3. Hoffmann bromamide reaction.
4. None of the above.
If D is N-methyl aniline in the reaction below, then A is:
\(\text A\xrightarrow{\bf\text{ reduction }}\text B\xrightarrow{\bf\text {CHCl}_3\text{/KOH}}\text C\xrightarrow{\bf\text{ reduction }}\text D\)
1. | 2. | ||
3. | CH3NH2 | 4. |
The final product C, obtained in this reaction, would be:
1. | 2. | ||
3. | 4. |
Aniline when diazotized in cold and then treated with dimethyl aniline gives a coloured product. Its structure would be:
1. | |
2. | |
3. | |
4. |
Electrolytic reduction of nitrobenzene in weakly acidic medium gives:
1. Aniline
2. p-Hydroxy aniline
3. N-Phenyl hydroxyl amine
4. Nitroso benzene
Aniline in a set of reactions yielded a product D
The structure of the product D would be:
1.
2.
3.
4.