The type of isomerism shown by C6H5CN and C6H5NC is:

1. Position

2. Functional

3. enantiomer

4. Tautomerism

Subtopic:  Amines - Preparation & Properties |
 84%
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The product D in the following sequence of reactoins is, 

CH3COOH NH3 A Heat B P2O5 C Na + C2H5OH D :

1. Ester

2. Amine

3. Acid

4. Alcohol

Subtopic:  Amines - Preparation & Properties |
 70%
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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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What is the decreasing order of the basicity of 1°, 2° and 3° ethyl amines (in aquous) and ammonia ?

1. NH3>C2H5NH2>(C2H5)2NH>(C2H5)3N

2. (C2H5)3N>(C2H5)2NH>C2H5NH2>NH3

3. (C2H5)2NH>C2H5NH2>(C2H5)3N>NH3

4. (C2H5)2NH>(C2H5)3N>C2H5NH2>NH3

 

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
 61%
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An aromatic primary amine with cold nitrous acid leads to the formation of:

1. alcohol

2. nitrite

3. diazonium salt

4. benzene

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
 73%
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The least basic aqueous solution among the following is:

1. (CH3)2NH

2. CH3NH2

3. (CH3)3N

4. C6H5NH2

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
 61%
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Which one of the following on reduction with LiAlH4 yields a secondary amine ?

[2007]

1. Methyl isocyanide

2. Acetamide

3. Methyl cyanide

4. Nitroethane

Subtopic:  Identification of Primary, Secondary & Tertiary Amines | Cyanides & Isocyanides |
 78%
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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 |
 86%
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In the reaction,

CH3CN+2HSnCl2HClX Boiling H2O Y, the term Y is 

[1999]

1. Acetone

2. Ethanamine

3. Acetaldehyde

4. Dimethyl amine

Subtopic:  Cyanides & Isocyanides |
 56%
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RMgX on reacting with cyanogen chloride gives:

1. R-NC

2. R-Cl

3. R-CN

4. None of the above

Subtopic:  Cyanides & Isocyanides |
 59%
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