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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 Organic Compounds Containing Nitrogen

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What are the starting reagents needed to make the azo compound shown below?

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Which of the following reactions is used to prepare aryl fluorides from diazonium salts and fluoroboric acid?
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Coupling of benzene diazonium chloride with 1-naphthol in alkaline medium will give:
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Reaction of aniline with NaNO2+ dil. HCl at 0o C followed by reaction with CuCN yields
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In a set of reactions p- nitrotoluene yielded a product E

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Product E would be:

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For the identification of β -naphthol using dye test, it is necessary to use
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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
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Benzene diazonium chloride on reaction with aniline in the presence of dilute hydrochloric acid gives:
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The reaction of Benzene diazonium chloride with aniline yields a yellow dye. The name of the yellow dye is
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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?
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The reagent (s) used for the conversion of benzene diazonium hydrogensulfate to benzene is/are
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Products A and B formed in the following reactions are respectively:

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