The chemical test used to distinguish between aniline and benzylamine is-

1. Nitrous acid.

2. Reduction Reaction

3. Hinsberg reagent

4. None of above

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
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The chemical test used to distinguish between aniline and N-methyl aniline is-

1. Carbylamine test 

2. Hoffmann bromamide reaction

3. Acetylation

4. None of above

 

 

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
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The chemical test used to distinguish between methylamine and dimethylamine is-

1. Hoffmann bromamide reaction

2. Hinsberg's reagent 

3. Carbylamine test

4. Both 2 and 3

 

 

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
 76%
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X, Y, and Z in the above sequence are -

1. X= Fe/HCl, Y= Br2/FeCl3, and Z = H2O/ warm

2. X= Br2/FeCl3, Y= Fe/HCl, and Z = H2O/ warm

3.  X= HBr/ hv, Y= Fe/HCl, and Z = H3PO2

4. X = HBr/ hv Y = Br2/FeCl3, and Z = H3PO2

 

Subtopic:  Amines - Preparation & Properties |
 86%
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X, and Y in the following sequence are :

1. X =  Br2 / CS2 , and Y =  
2. X =  Br2 / H2O  and Y =
3. X =  Br2 / CS2 , and Y = 
4. X =  Br2 / H2O  and Y = 

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 83%
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Benzyl chloride KCN X LiAlH4 Y

The product X and Y are -

1. 2-Phenylethanenitrile and Benzoic acid

2. Benzonitrile and Benzoic acid

3. 2-Phenylethanenitrile and 2-Phenylethanamine

4. Benzonitrile and 2-Phenylethanamine

Subtopic:  Amines - Preparation & Properties |
 55%
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The IUPAC name of X and Y in the following reaction sequence are:

Chlorobenzene HNO3, H2SO4 X H2/Pd Y

1. 1-Chloro-4-nitrobenzene, and Nitrobenzene

2. 1-Chloro-3-nitrobenzene, and 4-Chloroaniline

3. 1-Chloro-4-nitrobenzene, and 4-Chloroaniline

4. 1-Chloro-3-nitrobenzene, and Nitrobenzene

Subtopic:  Mechanism |
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Benzamide  Br2, NaOH A 2. H3PO21. HNO2 Benzene CH3Cl, AlCl3
B

A and B in the above reaction sequence are -

1. Chlorobenzene and aniline

2. Aniline and toluene

3. p-Methylaniline and chlorobenzene

4. None of the above

 

 

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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\(\small{\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{I} \xrightarrow[]{NaCN} \mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CN}\xrightarrow[]{{OH}^{-},Partial hydrolysis} A \xrightarrow[NaOH]{{Br}_2} \mathrm{B}}\)

The molecular formulae of A, and B in the above reaction are-

1. CH3CH2COOH, and CH3CH(Br)COOH
2. CH3CH2COOH, and CH3CH2COBr
3. CH3CH2CONH2, and CH3CH2NH2
4. CH3CH2CONH2, and CH3CH2CH2NH2

Subtopic:  Mechanism |
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The formula of A and B in the following reaction is -

C6H5N2Cl  CuCN C6H5CN  H2O /H+  A NH3 ,B

 1. C6H5COOH, and C6H5CONH2
2. C6H5COOH, and C6H5NH2
3. C6H5CH2NH2, and C6H5CH2N=NH
4. C6H5CH2NH2, and  C6H5CH2N=NH

Subtopic:  Amines - Preparation & Properties |
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