In a set of reactions, propanoic acid yielded a compound (D).

\(CH_3CH_2COOH\ \text{(A)} \xrightarrow[]{SOCl_2}\ \text{(B)} \)
\(\ \xrightarrow[]{NH_3}\ \text{(C)}\ \xrightarrow[Br_2]{KOH}\ \text{(D)}\)

The formula for (D) is:

1. CH3CH2CH2NH2

2. CH3CH2CONH2

3. CH3CH2NHCH3

4. CH3CH2NH2

Subtopic:  Amines - Preparation & Properties |
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Aniline in a set of reactions yielded a product D.
\(\xrightarrow[HCl]{NaNO_2}\ A\ \xrightarrow[]{CuCN}\ B\ \xrightarrow[Ni]{H_2}\ C\ \xrightarrow[]{HNO_2}\ D\)

The formula of the product D in the above mentioned reaction is

1. C6H5NHOH

2. C6H5NHCH2CH3

3. C6H5CH2NH2

4. C6H5CH2OH

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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Benzene diazonium chloride on reaction with aniline in the presence of dilute hydrochloric acid gives:

1.  2.  
3.   4.  
 

Subtopic:  Mechanism |
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CH3CH2CO-NH2 can be converted into CH3CH2NH2 in the presence of:

1. LiAlH4 

2. H2/Pt

3. Sn/HCl 

4. NaOBr/OH

Subtopic:  Amines - Preparation & Properties |
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Which of the following compounds, when reduced with lithium aluminium hydride, produces a secondary amine?

1. Nitroethane

2. Methylisocyanide

3. Acetamide

4. Methyl cyanide

Subtopic:  Amines - Preparation & Properties |
 78%
From NCERT
AIPMT - 2007
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The product B in the below mentioned reaction is:
\(Acetamide \overset{P_2O_5}{\longrightarrow}A\ \overset{4H}{\longrightarrow}\ B\)

1. CH3NH                             

2. C2H5NH2

3. CH3CN                                   

4. CH3COONH4

Subtopic:  Amines - Preparation & Properties |
 66%
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Z in the below reaction sequence will be:
\(CH_3CH_2Cl \)\(\xrightarrow[]{NaCN}\ X\ \)\(\xrightarrow[]{Ni/H_2}\ Y \ \)\(\xrightarrow{Ac_2O}\ Z\)
1. \(\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_2 \mathrm{NHCOCH}_3 \)
2. \(\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_2 \mathrm{NH}_2 \)
3. \(\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_2 \mathrm{CONHCH}_3 \)
4. \(\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_2 \mathrm{CONHCOCH}_3\)

Subtopic:  Cyanides & Isocyanides |
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A(C3H9N) reacts with benzenesulfonyl chloride to give an insoluble salt in alkali.

The structure of compound (A) will be:

1. CH3CH2CH2NH2 2. CH3NHCH2CH3
3. 4. None of the above
Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
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What is the correct order of the methyl-substituted amines' basic strength in an aqueous solution?

1. CH3NH> (CH3)2NH > (CH3)3N

2. (CH3)2NH > CH3NH2 > (CH3)3N

3. (CH3)3N > CH3NH2 > (CH3)2NH

4. (CH3)3N > CH3NH2 > (CH3)2NH

Subtopic:  Amines - Preparation & Properties |
 75%
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NEET - 2019
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 The structure of C in the below-mentioned reaction is: 

1. 
2.
3.
4.
Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 85%
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AIPMT - 2008
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