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The products formed when Aniline reacts with Br2 water, and NaNO2/HCl 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
Subtopic:  Amines - Preparation & Properties |
 86%
Level 1: 80%+
AIPMT - 1998
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Which chemical reaction leads to the formation of isocyanide?

1. Reimer Tiemann reaction.
2. Carbylamine reaction.
3. Hoffmann bromamide reaction.
4. None of the above.

Subtopic:  Amines - Preparation & Properties |
 90%
Level 1: 80%+
AIPMT - 1999
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D is N-methyl aniline in the given below sequence of reaction:
\(\text A\xrightarrow{\bf\text{ reduction }}\text B\xrightarrow{\bf\text {CHCl}_3\text{/KOH}}\text C\xrightarrow{\bf\text{ reduction }}\text D\)

Structure of A can be:

1.   2.
3.  
\(\mathrm{CH_3NH_2 }\)
4.
Subtopic:  Amines - Preparation & Properties |
 70%
Level 2: 60%+
AIPMT - 2000
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The final product C, obtained in this reaction, would be:

1. 2.
3. 4.
Subtopic:  Amines - Preparation & Properties |
 75%
Level 2: 60%+
AIPMT - 2003
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Aniline when diazotized in cold and then treated with dimethyl aniline gives a coloured product. Its structure would be:

1.
2.
3.
4.
Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 78%
Level 2: 60%+
AIPMT - 2004
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Electrolytic reduction of nitrobenzene in weakly acidic medium gives:

1. Aniline

2. p-Hydroxy aniline

3. N-Phenyl hydroxyl amine

4. Nitroso benzene

Subtopic:  Urea & Nitro Compound |
 69%
Level 2: 60%+
AIPMT - 2005

Sorry!! currently, the explanation for the question is not provided. If you need further help, please email at support@neetprep.com with subject: Explanation Missing for Question Id: 264091

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Aniline in a set of reactions yielded a product D

 

The structure of the product D would be:

1. C6H5CH2OH

2. C6H5CH2NH2

3. C6H5NHOH

4. C6H5NHCH2CH3

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 76%
Level 2: 60%+
AIPMT - 2005
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