How is aniline prepared commercially? Describe carbylamines tes

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 Multiple Choice QuestionsLong Answer Type

181.

Identify the substances A and B in each of the following sequences of reactions:



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 Multiple Choice QuestionsShort Answer Type

182.

Identify the substances A and B in each of the following sequences of reactions:
CH3CONH2 is a weaker base than CH3CH2NH2

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183.

ROH is a stronger acid than RNH2.

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184.

Show how p-amino azobenzene can be prepared from aniline?

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185.

Explain the following reactions by taking one suitable example in each case:
Hoffmann's bromamide reaction.

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186.

Explain the following reactions by taking one suitable example in each case:
Gattermann’s reaction.

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187.

How is ethylamine prepared from acetonitrile? Compare its basic character with that of ammonia.

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 Multiple Choice QuestionsLong Answer Type

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188.

How is aniline prepared commercially? Describe carbylamines test for primary amines.


Aniline is prepared commercially by the reduction of nitrobenzene using iron and hydrochloric acid.



Because of the presence of hydrochloric acid in the reaction mixture actually aniline hydrochloride (C
6H5NH3+Cl-) is obtained. This on treatment with aqueous sodium carbonate gives aniline.



Carbylamine test for primary amines:
Primary amines, both aliphatic and aromatic, give carbylamines having a pungent smell, when heated with chloroform and alcoholic potash.


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189.

Describe the method for the identification of primary, secondary and tertiary amines. Also write chemical equations of the reactions involved.

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 Multiple Choice QuestionsShort Answer Type

190. Write IUPAC names of following and classify them into primary, secondary, tertiary amines:
(CH3)2CHNH2
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