The correct increasing order of basic strength for the following compounds is:

   (I)       (II)       (III)

1. II < III < I

2. III < I < II

3. III < II < I

4. II < I < III

Subtopic:  Amines - Preparation & Properties |
 86%
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Methylamine reacts with HNO2 to form-

1. CH3-O-N=O 2. CH3-O-CH3
3. CH3-OH 4. CH3CHO
Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 74%
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The gas evolved when methylamine reacts with nitrous acid is .............

1. NH3
2. N2
3. H2
4. C2H6

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 85%
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In nitration of benzene using a mixture of conc. H2SO4 and conc. HNO3, the species that initiates the reaction is :

1. NO2
2. NO+
3. NO2+
4. NO2-

Subtopic:  Urea & Nitro Compound |
 78%
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Reduction of aromatic nitro compounds using Fe and HCl gives:

1.  Aromatic oxime

2.  Aromatic hydrocarbon

3.  Aniline

4.  Aromatic amide

Subtopic:  Amines - Preparation & Properties |
 90%
From NCERT
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The most reactive amine towards dilute hydrochloric acid is:

1. 2.
3. 4.
Subtopic:  Amines - Preparation & Properties |
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Acid anhydrides on reaction with primary amines give:

1.  Amide

2.  Imide

3.  Secondary amine

4.  Imine

Subtopic:  Mechanism |
 66%
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The following reaction is named as:

\(\mathrm{Ar} \mathrm{N}_2^{+} \mathrm{Cl}^{-} \xrightarrow{\mathrm{Cu}/ \mathrm{HCl}} \mathrm{ArCl}+\mathrm{N}_2+\mathrm{CuCl}\)
1. Sandmeyer reaction
2. Gattermann reaction
3. Claisen reaction
4. Carbylamine reaction

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 73%
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Which of the following compound will not undergo azo coupling reaction with benzene diazonium chloride?

1.  Aniline

2.  Phenol

3.  Anisole

4.  Nitrobenzene

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 64%
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A compound among the following that does not undergo an azo coupling reaction with benzene diazonium chloride is:

1. Aniline

2. Phenol

3. Anisole

4. Nitrobenzene

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 60%
From NCERT
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