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Benzene diazonium chloride on reaction with aniline in the presence of dilute hydrochloric acid gives

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Important Questions on Amines

EASY
Benzene diazonium chloride on reaction with aniline in the presence of dilute hydrochloric acid gives:
HARD
In the reaction,

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The product E is
MEDIUM
Coupling of benzene diazonium chloride with 1-naphthol in alkaline medium will give:
MEDIUM
Reaction of aniline with NaNO2+ dil. HCl at 0o C followed by reaction with CuCN yields
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HARD

Consider the following reaction:
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The product 'X' is used:

HARD

The major product of the following reaction is

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EASY
Action of NaNO2 with dilute HCl on ArNH2 yields ArN2+Cl-. A similar reaction with cyclohexylamine will yield
HARD

In a set of reactions p- nitrotoluene yielded a product E

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Product E would be:

MEDIUM
Fluorination of an aromatic ring is easily accomplished by treating a diazonium salt with HBF4. Which of the following conditions is correct about this reaction?
EASY
Which of the following is a Gattermann reaction?
HARD
Products A and B formed in the following reactions are respectively:

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MEDIUM
In the following reaction, the product (A)
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EASY
The reaction of Benzene diazonium chloride with aniline yields a yellow dye. The name of the yellow dye is
EASY
C6H5N2Cl in presence of KCN and CuCN gives an organic compound, which on acid hydrolysis gives ' X ' The compound ' X ' may be
EASY
Which of the following is not a chromophore?
MEDIUM
For the identification of β -naphthol using dye test, it is necessary to use
MEDIUM
The reagent (s) used for the conversion of benzene diazonium hydrogensulfate to benzene is/are
HARD
A given nitrogen-containing aromatic compound A reacts with Sn/HCl, followed by HNO2 to give an unstable compound B. B on treatment with phenol, forms a beautiful coloured compound C with the molecular formula C12H10N2O. The structure of compound A is