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NEET-UG and JEE Main Chemistry · Class 12

Oxidation, reduction and distinguishing tests — NEET & JEE Questions

Oxidation, reduction and distinguishing tests is a topic in Organic Compounds Containing Oxygen, a Class 12 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 26 published NEET-UG and JEE Main questions on Oxidation, reduction and distinguishing tests, each with the marking scheme of the real paper.

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Oxidation, reduction and distinguishing tests MCQs with solutions

10 of the 26 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

    Controlled oxidation of a primary alcohol can first produce an

    • A. aldehyde
    • B. ketone
    • C. alkane
    • D. ether
  2. Question 2 · difficulty L2 · understanding

    A student is given one compound among the following compounds that gives positive test with Tollen's reagent. The compound is :

    • A. B
    • B. D
    • C. A
    • D. C
  3. Question 3 · difficulty L2 · understanding

    Which of the following compounds will give silver mirror with ammoniacal silver nitrate? A. Formic acid B. Formaldehyde C. Benzaldehyde D. Acetone Choose the correct answer from the options given below :

    • A. B and C only
    • B. C and D only
    • C. A, B and C only
    • D. A only
  4. Question 4 · difficulty L2 · understanding

    Which among the above compound/s does/do not form Silver mirror when treated with Tollen's reagent?

    • A. (I), (III) and (IV) only
    • B. Only (IV)
    • C. Only (II)
    • D. (III) and (IV) only
  5. Question 5 · difficulty L2 · understanding

    2, 4-DNP test can be used to identify :

    • A. ether
    • B. amine
    • C. aldehyde
    • D. halogens
  6. Question 6 · difficulty L2 · understanding

    The spin only magnetic moment of the complex present in Fehling's reagent is __________ B.M. (Nearest integer).

  7. Question 7 · difficulty L2 · understanding

    In Tollen's test for aldehyde, the overall number of electron(s) transferred to the Tollen's reagent formula [Ag(NH 3 ) 2 ] + per aldehyde group to form silver mirror is ___________. (Round off to the Nearest Integer).

  8. Question 8 · difficulty L3 · understanding

    An optically active alkyl bromide C4H9Br\mathrm{C}_4 \mathrm{H}_9 \mathrm{Br}, reacts with ethanolic KOH to form major compound [A][\mathrm{A}] which reacts with bromine to give compound [B][\mathrm{B}]. Compound [B][\mathrm{B}] reacts with ethanolic KOH and sodamide to give compound [C]. One molecule of water adds to compound [C] on warming with mercuric sulphate and dilute sulphuric acid at 333 K to form compound [D]. The functional group in compound D will be confirmed by :

    • A. Haloform test
    • B. Lucas test
    • C. Silver mirror test
    • D. Benedict test
  9. Question 9 · difficulty L3 · understanding

     Given below are the four isomeric compounds (P,Q,R, S) \text { Given below are the four isomeric compounds }(\mathrm{P}, \mathrm{Q}, \mathrm{R}, \mathrm{~S}) Identify correct statements from below. A. Q,R\mathrm{Q}, \mathrm{R} and S will give precipitate with 2, 4-DNP. B. PP and QQ will give positive Bayer's test. C. Q and R will give sooty flame. D. R and S will give yellow precipitate with I2/NaOH\mathrm{I}_2 / \mathrm{NaOH}. E. Q alone will deposit silver with Tollen's reagent Choose the correct option.

    • A. C and E only
    • B. A and E only
    • C. A, B, D and E only
    • D. A, C and E only
  10. Question 10 · difficulty L3 · understanding

    The unsaturated ether on acidic hydrolysis produces carbonyl compounds as shown below :- Based on this, predict the solution/reagent that will help to distinguish "P" and "Q" obtained in the following reaction :-

    • A. Saturated NaHSO3\mathrm{NaHSO}_3 solution
    • B. Fehling solution
    • C. Lucas reagent
    • D. 2, 4 - DNP reagent

Common mistakes in Oxidation, reduction and distinguishing tests

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.

  • Assumes aldehydes and ketones behave identically toward mild oxidants.
  • Assigns typical aldehyde oxidation behaviour to a ketone.
  • Assumes all carbonyl compounds give the same oxidation test.

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