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Chemistry

NEET Chemistry / AI question bank / NCERT Class 12 / Organic Compounds Containing Nitrogen

Amines: NEET questions with solutions

NEET tests the basicity order of amines in water and in the gas phase, Gabriel and Hoffmann methods, the carbylamine and Hinsberg tests, why aniline gives meta product on nitration, and diazonium salt reactions such as Sandmeyer and coupling. Marks are lost on the aqueous basicity order and on which amine class a test identifies.

Also called: amines and diazonium salts · basicity of amines

Questions

10 questions / answers after you pick

  1. Q1Which compound gives a foul-smelling isocyanide when warmed with chloroform and alcoholic KOH?

    Reactions of aminesEasySingle correct

  2. Q2Why can Gabriel phthalimide synthesis not be used to prepare aniline?

    Preparation of aminesEasySingle correct

  3. Q3Propanamide (CH₃CH₂CONH₂) is treated with Br₂ and aqueous NaOH. What amine forms?

    Preparation of aminesEasySingle correct

  4. Q4Which order of basic strength in aqueous solution is correct?

    Basic character of aminesMediumSingle correct

  5. Q5Why is aniline a weaker base than methanamine?

    Basic character of aminesMediumSingle correct

  6. Q6Direct nitration of aniline with a nitrating mixture gives a considerable amount of meta-nitroaniline. Why?

    Electrophilic substitution in anilineMediumSingle correct

  7. Q7Benzenesulphonyl chloride (Hinsberg's reagent) is used to tell apart primary, secondary and tertiary amines. Judge the Assertion (A) and the…

    Hinsberg's testMediumAssertion–Reason

  8. Q8Arenediazonium salts are prepared from aromatic amines and used widely in synthesis. Which of the statements below are correct?

    Diazonium saltsMediumStatement based

  9. Q9Benzenediazonium chloride is treated with each reagent in List I. Match each reagent with the main organic product in List II.

    Reactions of diazonium saltsHardMatch the following

  10. Q10Which sequence converts aniline into 1,3,5-tribromobenzene?

    Diazonium salts in synthesisHardSingle correct

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