Skip to content

NEET-UG and JEE Main Chemistry · Class 11

Ozonolysis and oxidation of alkenes — NEET & JEE Questions

Ozonolysis and oxidation of alkenes is a topic in Hydrocarbons, a Class 11 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 12 published NEET-UG and JEE Main questions on Ozonolysis and oxidation of alkenes, each with the marking scheme of the real paper.

questions
12
shown here
10
Test me on this topic

Five free tests with an account. Your score comes with the result; where you stand is Pro.

Ozonolysis and oxidation of alkenes MCQs with solutions

10 of the 12 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

    Ozonolysis of an alkene followed by reductive workup cleaves the C=C bond to form mainly

    • A. carbonyl compounds
    • B. alkanes only
    • C. alcohols only
    • D. amines
  2. Question 2 · difficulty L2 · understanding

    Ozonolysis is useful in structure determination because it reveals

    • A. the substitution pattern around the original C=C bond
    • B. only the molecular mass
    • C. only the number of hydrogens in the whole molecule
    • D. the boiling point
  3. Question 3 · difficulty L2 · understanding

    Cold dilute alkaline KMnO4KMnO_4 typically converts an alkene into

    • A. a vicinal diol
    • B. an alkane
    • C. an amine
    • D. a nitrile
  4. Question 4 · difficulty L2 · understanding

    Strong oxidative cleavage of an alkene differs from reductive ozonolysis because aldehyde fragments may be further oxidised to

    • A. carboxylic acids
    • B. alkanes
    • C. amines
    • D. ethers
  5. Question 5 · difficulty L3 · application

    Ozonolysis of ethene followed by reductive workup gives

    • A. methanal
    • B. ethanal
    • C. propanone
    • D. methanol
  6. Question 6 · difficulty L3 · application

    Reductive ozonolysis of propene gives

    • A. methanal and ethanal
    • B. two ethanal molecules
    • C. methanal and propanone
    • D. ethanoic acid and methanal
  7. Question 7 · difficulty L3 · application

    Ozonolysis of 2-methylpropene followed by reductive workup gives

    • A. propanone and methanal
    • B. ethanal and methanal
    • C. two molecules of propanone
    • D. propanone and methanol
  8. Question 8 · difficulty L3 · application

    An alkene rapidly decolourises cold dilute alkaline permanganate. This observation is consistent with

    • A. oxidation of the C=C bond to a vicinal diol
    • B. formation of an alkane without oxidation
    • C. absence of unsaturation
    • D. formation of an amide
  9. Question 9 · difficulty L4 · application

    An alkene gives only propanone on reductive ozonolysis. Which alkene is most consistent?

    • A. 2,3-Dimethylbut-2-ene
    • B. But-2-ene
    • C. Propene
    • D. 2-Methylpropene
  10. Question 10 · difficulty L4 · application

    An alkene gives ethanal as the only carbonyl product on reductive ozonolysis. Which alkene is indicated?

    • A. But-2-ene
    • B. Propene
    • C. Ethene
    • D. 2-Methylpropene

Common mistakes in Ozonolysis and oxidation of alkenes

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.

  • Uses carbonyl carbon count without reconstructing substituents on each original alkene carbon.
  • Assumes strong oxidation preserves aldehydes formed in reductive ozonolysis.

Practise this chapter

Reading a question and answering it under a clock are different things. A chapter-length test measures whether the topic went in.