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Test for Amines - Practice Questions & MCQ

Edited By admin | Updated on Sep 25, 2023 25:24 PM | #NEET

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  • Test for Amines, Carbylamine Test, Reaction with NaNO2 + HCl is considered one of the most asked concept.

  • 45 Questions around this concept.

Solve by difficulty

Which one of the following methods is neither meant for the synthesis nor for separation of amines?

The product formed by the reaction of an aldehyde with a primary amine is

The reaction of chloroform with alcoholic KOH and p-Toluidine forms

When primary amine reacts with chloroform in ethanolic KOH then the product is

In the chemical reaction, \mathrm{CH_{3}CH_{2}NH_{2}+CHCl_{3}+3KOH\rightarrow (A)+(B)+3H_{2}O,}  the compounds \mathrm{(A)\; and\; (B)} are respectively

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On heating an aliphatic primary amine with chloroform and ethanolic potassium hydroxide, the organic compound formed is:

An organic compound (C3H9N) (A), when treated with nitrous acid, gave an alcohol and N2 gas was evolved. (A) on warming with CHCl3 and caustic potash gave (C) which on reduction gave isopropylmethylamine. Predict the structure of (A).

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The following reaction

is known by the name:

 The final product formed when Methyl  amine is treated with \mathrm{NaNO_2} and \mathrm{HCl} is

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Some reactions of amines are given. Which one is not correct?

Concepts Covered - 4

Test for Amines

Libermann Nitroso Test
While phenol is reacted with NaNO2 and concentrated H2SO4, it provides a deep green or blue colour which changes to red on dilution with water. while generated alkaline along with NaOH original green or blue colour is restored. This reaction is termed as Liebermann's nitroso reaction and is employed as a test of phenol. Libermann's nitroso test is used as a test for secondary amines.

Hoffmann's Test
Separation of primary, secondary and tertiary amines by Hoffmann's method. The mixture of three amines is treated with diethyl oxalate. The primary amine forms a solid oxamide, a secondary amine gives a liquid oxamic ester while tertiary amine does not react.

Hinsberg's Test
The Hinsberg test which is used to distinguish between primary, secondary, and tertiary amines, is based upon sulfonamide formation. In this test, an amine is reacted with benzene sulfonyl chloride. If a product forms, the amine is either a primary or secondary amine, because tertiary amines do not form stable sulfonamides. If this sulfonamide that formed is dissolved in aqueous sodium hydroxide solution, it is a primary amine. But if is insoluble in aqueous sodium hydroxide then it is a secondary amine. The sulfonamide of a primary amine is soluble in an aqueous base because it still possesses an acidic hydrogen on the nitrogen, which can be lost to form a sodium salt.

Hoffmann's Mustard Oil Reaction
When ethylamine is heated with carbon disulphide and mercuric chloride, ethyl isothiocyanate is formed which has smell like mustard oil.

\mathrm{C_{2}H_{5}NH_{2}\: +\: CS_{2}\: +\: HgCl_{2}\: \rightarrow \: C_{2}H_{5}NCS\: +\: HgS\: +\: 2HCl}

Carbylamine Test

When any primary amine(aliphatic or aromatic) is heated with chloroform and alcoholic potassium hydroxide solution, isocyanide(carbylamine) is formed which has a very unpleasant smell. This test is called carbylamine test or isocyanide test. The reactions occur as follows:

\\\mathrm{C_{2}H_{5}NH_{2}\: +\: CHCl_{3}\: +\: 3KOH\: \rightarrow \: C_{2}H_{5}NC\: +\: 3KCl\: +\: 3H_{2}O}\\\\\mathrm{C_{6}H_{5}NH_{2}\: +\: CHCl_{3}\: \rightarrow \: C_{6}H_{5}NC\: +\: 3KCl\: +\: 3H_{2}O}

Alkylation and Acylation of Amines

Alkylation
Amines undergo alkylation with RX and undergo complete methylation and this is called exhaustive methylation, but with Me2SO4 amines undergo monomethylation. 1o and 2o amines are also methylated by heating HCHO and excess of HCOOH at 100oC. This reaction is known as Eschweiler-Clarke methylation. The reaction occurs as follows:

Acylation
1o and 2o aliphatic and aromatic amines react with acid chlorides (RCOCl), anhydrides and esters by SN2 reaction is called acylation reaction. The reaction is carried out in the presence of a base stronger than amine, such as pyridine, which removes HCl so formed and shifts the equilibrium to the product side. The reaction occurs as follows:

Reaction with NaNO2 + HCl

Nitrous acid(HNO2) is obtained in situ by the reaction of sodium nitrite (NaNO2) with dil. HCl. The reaction occurs as follows:

\mathrm{NaNO_{2}\: +\: HCl\: \rightarrow \: HNO_{2}\: +\: NaCl}

1o aliphatic amines react with HNO2 to form aliphatic diazonium salts, which, being unstable, liberate N2 gas quantitatively and alcohols. Quantitative evolution of N2 is used in the estimation of amino acids and proteins. The reaction occurs as follows:

Mechanism

 

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Test for Amines
Carbylamine Test
Alkylation and Acylation of Amines

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Books

Reference Books

Carbylamine Test

Chemistry Part II Textbook for Class XII

Page No. : 401

Line : 1

Alkylation and Acylation of Amines

Chemistry Part II Textbook for Class XII

Page No. : 400

Line : 9

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