Product Q in the above reaction is

1.

2.

3.

4.

Subtopic: Cyanides & Isocyanides |

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The final product C in the below mentioned reaction is:
$\xrightarrow[]{Ac_2O}\ A\ \xrightarrow[CH_3COOH]{Br_2}\ B\ \xrightarrow[H^+]{H_2O}\ C$

1.		2.
3.		4.

Subtopic: Mechanism |

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Aniline when diazotised in cold and then treated with dimethylaniline, gives a coloured product. Its structure would be :

Subtopic: Diazonium Salts: Preparation, Properties & Uses |

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Aniline in a set of the following reactions yielded a coloured product Y.

$\to_{(273 - 278 K)}^{{NaNO}_{2} / HCl} X \overset{N, N - dimethylaniline}{\to} Y$

The structure of Y would be

Subtopic: Amines - Preparation & Properties |

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What is the end product in the following sequences of operations;

Acetamide $\overset{P_{2} O_{5}}{\to} A \overset{4 H}{\to} B$ ?

1. CH₃NH₂

2. C₂H₅NH₂

3. CH₃CN

4. CH₃COONH₄

Subtopic: Mechanism |

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Name the end product in the following series of reactions,

CH₃COOH $\overset{{NH}_{3}}{\to}$ A $\overset{∆}{\to}$ B $\overset{P_{2} O_{5}}{\to}$ C:

1. CH₄

2. CH₃OH

3. acetonitrile

4. ammonium acetate

Subtopic: Amines - Preparation & Properties |

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are ........... isomers.

1.Chain

2. functional

3. position

4. all of these

Subtopic: Amines - Preparation & Properties | Urea & Nitro Compound |

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Primary nitroalkanes on hydrolysis give:

1. RCOOH + NH₂OH

2. RCOOH

3. NH₂OH

4. RCOR

Subtopic: Mechanism |

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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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The type of isomerism shown by C₆H₅CN and C₆H₅NC is:

1. Position

2. Functional

3. enantiomer

4. Tautomerism

Subtopic: Amines - Preparation & Properties |

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Select Question Set:

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Product Q in the above reaction is

1.

2.

3.

4.

Select Question Set:

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Product Q in the above reaction is 1. 2. 3. 4.

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Product Q in the above reaction is

1.

2.

3.

4.