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NEET-UG and JEE Main Chemistry · Class 12

Diazonium salts - preparation, reactions and synthetic importance — NEET & JEE Questions

Diazonium salts - preparation, reactions and synthetic importance is a topic in Organic Compounds Containing Nitrogen, a Class 12 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 60 published NEET-UG and JEE Main questions on Diazonium salts - preparation, reactions and synthetic importance, each with the marking scheme of the real paper.

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Diazonium salts - preparation, reactions and synthetic importance MCQs with solutions

10 of the 60 published questions on this topic, exactly as they appear in a test. Answers and worked solutions come with your result rather than on this page.

  1. Question 1 · difficulty L1 · recall

    Benzenediazonium chloride is commonly prepared from aniline using nitrous acid generated in situ at

    • A. low temperature, about 0–5°C
    • B. about 100°C
    • C. red heat
    • D. any temperature with no effect
  2. Question 2 · difficulty L2 · understanding

    Given below are two statements I and II. Statement I : Dumas method is used for estimation of "Nitrogen" in an organic compound. Statement II : Dumas method involves the formation of ammonium sulphate by heating the organic compound with conc H2SO4\mathrm{H}_2 \mathrm{SO}_4. In the light of the above statements, choose the correct answer from the options given below

    • A. Statement I is true but Statement II is false
    • B. Statement I is false but Statement II is true
    • C. Both Statement I and Statement II are true
    • D. Both Statement I and Statement II are false
  3. Question 3 · difficulty L2 · understanding

    Given below are two statements : Statement I : Piciric acid is 2,4,6 - trinitrotoluene. Statement II : Phenol - 2,4 - disulphonic acid is treated with Conc. HNO3\mathrm{HNO}_3 to get picric acid. In the light of the above statements, choose the most appropriate answer from the options given below :

    • A. Statement I is incorrect but Statement II is correct
    • B. Both Statement I and Statement II are incorrect
    • C. Both Statement I and Statement II are correct
    • D. Statement I is correct but Statement II is incorrect
  4. Question 4 · difficulty L2 · understanding

    Which of the following nitrogen containing compound does not give Lassaigne's test ?

    • A. Glycene
    • B. Phenyl hydrazine
    • C. Urea
    • D. Hydrazine
  5. Question 5 · difficulty L2 · understanding

    A primary aliphatic amine on reaction with nitrous acid in cold (273 K) and there after raising temperature of reaction mixture to room temperature (298 K), gives a/an

    • A. nitrile
    • B. alcohol
    • C. diazonium salt
    • D. secondary amine
  6. Question 6 · difficulty L2 · understanding

    In the chemical reactions given above A and B respectively are :

    • A. H 3 PO 2 and CH 3 CH 2 Cl
    • B. CH 3 CH 2 OH and H 3 PO 2
    • C. H 3 PO 2 and CH 3 CH 2 OH
    • D. CH 3 CH 2 Cl and H 3 PO 2
  7. Question 7 · difficulty L2 · understanding

    Number of amine compounds from the following giving solids which are soluble in NaOH\mathrm{NaOH} upon reaction with Hinsberg's reagent is _________.

  8. Question 8 · difficulty L2 · understanding

    9.3 g9.3 \mathrm{~g} of pure aniline upon diazotisation followed by coupling with phenol gives an orange dye. The mass of orange dye produced (assume 100% yield/conversion) is ________ g. (nearest integer)

  9. Question 9 · difficulty L2 · understanding

    The compound formed by the reaction of ethanal with semicarbazide contains _________ number of nitrogen atoms.

  10. Question 10 · difficulty L3 · understanding

    Which of the following amino acid will give violet coloured complex with neutral ferric chloride solution?

    • A. Threonine
    • B. Serine
    • C. Tyrosine
    • D. Cysteine

Common mistakes in Diazonium salts - preparation, reactions and synthetic importance

Recorded against questions in this topic that are not shown above, so none of these points at an answer you can see on this page.

  • Treats the diazonium group as unreactive.

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