An aromatic primary amine with cold nitrous acid leads to the formation of:

(a) alcohol

(b) nitrite

(c) diazonium salt

(d) benzene

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 80%
Level 1: 80%+
Hints

Product P in the above reaction is 

[2002]

Subtopic:  Cyanides & Isocyanides |
 70%
Level 2: 60%+
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In the reaction sequence:

CH3CN+2HSnCl2HClXBoilingH2OY,
What is the compound Y?

1. Acetone

2. Ethanamine

3. Acetaldehyde

4. Dimethyl amine

Subtopic:  Cyanides & Isocyanides |
 63%
Level 2: 60%+
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X and Y in the given reaction are:

(a) CH3COOH+(CH3)2NH

(b) CH3CONH2+CH3OH

(c) CH3CHO+(CH3)2NH

(d) CH3COCH3+CH3NH2

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
 75%
Level 2: 60%+
Hints

Which of the following statements about primary amines is false ?

[2010]

(1) Alkyl amines are stronger bases than aryl amines

(2) Alkyl amines react with nitrous acid to produce alcohols

(3) Aryl amines react with nitrous acid to produce phenols

(4) Alkyl amines are stronger bases than ammonia

Subtopic:  Amines - Preparation & Properties |
 74%
Level 2: 60%+
AIPMT - 2010
Hints

Among the following, the strongest base is:

1. C6H5NH2

2. p-NO2-C6H4NH2

3. m-NO2-C6H4NH2

4. CH3CH2NH2

Subtopic:  Amines - Preparation & Properties |
 79%
Level 2: 60%+
Hints

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An amine reacts with C6H5SO2Cl and the product is soluble in alkali, amine is:

(a) 1°

(b) 2°

(c) 3°

(d) all of those

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
 87%
Level 1: 80%+
Hints

Among following reactions, the reaction does not yield an amine is-

1. 

2. 

3. 

4. 

Subtopic:  Cyanides & Isocyanides |
 66%
Level 2: 60%+
Hints

The end product in the following sequence of reactions is

C2H5NH2HNO2APCl5BNH3C?

1. Ethyl cyanide

2. Ethylamine

3. Methylamine

4. Acetamide

Subtopic:  Amines - Preparation & Properties |
 83%
Level 1: 80%+
Hints

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Identfy X in the sequence,

XHNO2C3H8OH2SO4K2Cr2O7C3H6O2 :

(a) CH3-NH-CH2-CH3

(b) CH3-CH2-CH2-NH2

(c) (CH3)3N

(d) none of the above

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
 85%
Level 1: 80%+
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