Primary, Secondary and tertiary amines may be separated by using:

1. ethanoyl chlorode

2. diethyl oxalate

3. thionyl chlorode

4. none of these

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
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The numbers of primary amines posible for the formula C4H11N is -

1. 1

2. 2

3. 3

4. 4

Subtopic:  Amines - Preparation & Properties |
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Aniline in a set of reactions yielded a product

[2005]

   

The structure of the product D would be

1. C6H5CH2NH2

2.  C6H5NHCH2CH3

3. C6H5NHOH

4. C6H5CH2OH

Subtopic:  Cyanides & Isocyanides | Diazonium Salts: Preparation, Properties & Uses |
 69%
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The IUPAC name of the compound having formula,

 O=CCHCH2
      |       |        |
    OH    NH2    OH is :

1. 3-Aminohydroxypropionic acid

2. 2-Amino-propan-3-oic acid

3. Amino hydroxy propionic acid

4. 2-Amino-3-hydroxy propanoic acid

Subtopic:  Amines - Preparation & Properties |
 85%
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X and Y in the given reaction are:

 

1. CH3COOH + (CH3)2NH

2. CH3CONH2 + CH3OH

3. CH3CHO + (CH3)2NH

4. CH3COCH3 + CH3NH2

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
 75%
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Dehydration of an amide gives:

1. Cyanide

2. Amine

3. Isocyanide

4. Fatty acid

Subtopic:  Cyanides & Isocyanides |
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Which can't give Hoffman's Rearrangement

1.

 

2.

3.

4.

1. 2.
3. 4.
Subtopic:  Amines - Preparation & Properties |
 63%
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Alkyl isocyanide on hydrolysis produces: 

1. Primary Amine 2. Tertiary Amine
3. Alcohol 4. Aldehyde
Subtopic:  Cyanides & Isocyanides |
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The major product of the following reaction would be

1. 
2.
3.
4.
Subtopic:  Amines - Preparation & Properties |
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C (major product) is

1. 
2.
3.
4. None of the above
Subtopic:  Amines - Preparation & Properties |
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