Chemical Reactions of Diazonium Salts

Author:Embibe Experts
JEE Main/Advance
IMPORTANT

Important Questions on Chemical Reactions of Diazonium Salts

EASY
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Benzenediazonium chloride can be converted into benzene on treatment with

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Statement-1: Aniline on reaction with NaNO2/HCl at 0 °C followed by coupling with β-naphthol gives a dark blue precipitate.

Statement-2 : The colour of the compound formed in the reaction of aniline with NaNO2/HCl at 0 °C followed by coupling with β-naphthol is due to the extended conjugation.

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Which of the following statement is CORRECT about product?

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Observe the following reaction and determine True statement

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C6H5N2ClSnCl2/HClAC6H5CHOB

The product (B) in the above sequence of reaction is

MEDIUM
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Complete reduction of benzene-diazonium chloride with Zn/HCl gives:

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The major product of the following reaction is:

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Coupling reaction takes place when benzene diazonium chloride is treated with:

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Ph-NO2Sn/HClHCl, 0°C-5°CNaNO2Ph-OHBasic medium Product Y

Find the molecular weight of Y report your answer as Molecular weight2.

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Question Image Product Z

Find the molecular weight of Z.

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How many toluidines on reaction with NaNO2/HCl followed by H3PO2 treatment gives toluene.

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The major product Y in the following sequence of reaction is:

Aniline (ii) CuCN/KCN(i) NaNO2/HCl, 273 K(X)(ii) H2O(i) DIBAL-H(Y)

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The structure of the final product (Y) formed in the following reaction sequence is:

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Para toluidine is treated with HNO2 at ice-cold conditions and then boiled with water. The final product obtained is:

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C6H5NH20-5°CNaNO2XH2OY, the product Y is:

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A solution contains 1 g mol each of p-toluene diazonium chloride and p-nitrophenyl diazonium chloride. To this 1 g mol of an alkaline solution of phenol is added. Predict the major product. Explain your answer. 

MEDIUM
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Which of the following compound will not undergo azo coupling reaction with benzene diazonium chloride.