Which of the following compound gives dye test

1. Aniline               

2. Methylamine                 

3. Diphenylamine                 

4. Ethylamine

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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Aniline in a set of reactions yield the following products                                                   

The structure of the product D would be -

1. C6H5CH2NH2

2. C6H5NHCH2CH3

3. C6H5NHOH

4. C6H5CH2OH

Subtopic:  Cyanides & Isocyanides | Diazonium Salts: Preparation, Properties & Uses |
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In a reaction of aniline a colored product C was obtained.

The structure of C would be

1. 

2. 

3. 

4. 

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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Aniline when diazotised in cold and then treated with dimethylaniline, gives a coloured product. Its structure would be :                                                                                 

1.

2. 

3. 

4. 

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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An aromatic primary amine with cold nitrous acid leads to the formation of:

1. alcohol

2. nitrite

3. diazonium salt

4. benzene

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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When NaNO2 and dilute HCl were added to an amine at 0°c, a colourless gas was evolved and an ionic compound is formed. The amine is:

1. any primary amine

2. an aromatic primary amine

3. any amine

4. none of the above

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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CH3CH2NH2 contains a basic NH2 group, but CH3CONH2 does not, because;

1. acetamide is amphoteric in character

2. in CH3CH2NH2 the electron pair on N-atom is delocalized by resonance

3. in CH3CH2NH2 there is no resonance, while in acetamide the lone pair of electron on N-atom is delocalized and therefore less available for protonation

4. none of the above

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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The above reaction is an example of....

1. Intermolecular C-N coupling
2. Intramolecular C-N coupling
3. Intermolecular N-N coupling
4. Intramolecular N-N coupling

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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In the below-mentioned reaction, the main byproduct (A) formed is:

1.  2.  
3.   4. None of these
 

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Product (B) of this reaction is:-
1. 

2. 

3. 

4.  

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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