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NEET-UG and JEE Main Chemistry · Class 11

Electrophiles, nucleophiles and stability of intermediates — NEET & JEE Questions

Electrophiles, nucleophiles and stability of intermediates is a topic in Some Basic Principles of Organic Chemistry, a Class 11 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 36 published NEET-UG and JEE Main questions on Electrophiles, nucleophiles and stability of intermediates, each with the marking scheme of the real paper.

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Electrophiles, nucleophiles and stability of intermediates MCQs with solutions

10 of the 36 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

    A nucleophile is a species that

    • A. donates an electron pair
    • B. accepts an electron pair
    • C. contains no electrons
    • D. must always be positively charged
  2. Question 2 · difficulty L2 · understanding

    Given below are two statements : Statement I : On the basis of inductive effect, the order of stability of alkyl carbanions is CH3−>CH3−CH2−>(CH3)2CH−>(CH3)3C−\mathrm{CH}_3{ }^{-}>\mathrm{CH}_3-\mathrm{CH}_2{ }^{-}>\left(\mathrm{CH}_3\right)_2 \mathrm{CH}^{-}>\left(\mathrm{CH}_3\right)_3 \mathrm{C}^{-}. Statement II : Allyl and benzyl carbanions are more stabilised by inductive effect and not by resonance effect. In the light of the above statements, choose the correct answer from the options given below :

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

    Given below are two statements : Statement I : In , the carbocation is stabilised by +R effect of –OCH 3 group. Statement II : In , the carbanion is stabilised by –R effect of –NO 2 group. In the light of the above statements, choose the correct answer from the options given below :

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

    CORRECT order of stability for the following is CH2=CH−,CH3−CH2−,CH≡C−\mathrm{CH}_2=\mathrm{CH}^{-}, \mathrm{CH}_3-\mathrm{CH}_2^{-}, \mathrm{CH} \equiv \mathrm{C}^{-}

    • A. CH≡C−>CH3−CH2−>CH2=CH−\mathrm{CH} \equiv \mathrm{C}^{-}>\mathrm{CH}_3-\mathrm{CH}_2^{-}>\mathrm{CH}_2=\mathrm{CH}^{-}
    • B. CH2=CH−>CH≡C−>CH3−CH2−\mathrm{CH}_2=\mathrm{CH}^{-}>\mathrm{CH} \equiv \mathrm{C}^{-}>\mathrm{CH}_3-\mathrm{CH}_2^{-}
    • C. CH≡C−>CH2=CH−>CH3−CH2−\mathrm{CH} \equiv \mathrm{C}^{-}>\mathrm{CH}_2=\mathrm{CH}^{-}>\mathrm{CH}_3-\mathrm{CH}_2^{-}
    • D. CH3−CH2−>CH2=CH−>CH≡C−\mathrm{CH}_3-\mathrm{CH}_2^{-}>\mathrm{CH}_2=\mathrm{CH}^{-}>\mathrm{CH} \equiv \mathrm{C}^{-}
  5. Question 5 · difficulty L2 · understanding

    Given below are two statements : Statement I : (CH3)3C⊕\left(\mathrm{CH}_3\right)_3 \stackrel{\oplus}{\mathrm{C}} is more stable than C⊕H3\stackrel{\oplus}{\mathrm{C}} \mathrm{H}_3 as nine hyperconjugation interactions are possible in (CH3)3C⊕\left(\mathrm{CH}_3\right)_3 \stackrel{\oplus}{\mathrm{C}}. Statement II : C⊕H3\stackrel{\oplus}{\mathrm{C}}\mathrm{H}_3 is less stable than (CH3)3C⊕\left(\mathrm{CH}_3\right)_3 \stackrel{\oplus}{\mathrm{C}} as only three hyperconjugation interactions are possible in C⊕H3\stackrel{\oplus}{\mathrm{C}} \mathrm{H}_3. In the light of the above statements, choose the correct answer from the options given below

    • A. Statement I is false but Statement II is true
    • B. Statement I is true but Statement II is false
    • C. Both Statement I and Statement II are true
    • D. Both Statement I and Statement II are false
  6. Question 6 · difficulty L2 · understanding

    Match the LIST-I with LIST-II LIST-I LIST-II A. Carbocation I. Species that can supply a pair of electrons. B. C-Free radical II. Species that can receive a pair of electrons. C. Nucleophile III. sp 2 hybridized carbon with empty p-orbital. D. Electrophile IV. sp 2 /sp 3 hybridized carbon with one unpaired electron. Choose the correct answer from the options given below:

    • A. A-IV, B-II, C-III, D-I
    • B. A-II, B-III, C-I, D-IV
    • C. A-III, B-IV, C-I, D-II
    • D. A-III, B-IV, C-II, D-I
  7. Question 7 · difficulty L2 · understanding

    Given below are two statements : Statement I : Hyperconjugation is not a permanent effect. Statement II : In general, greater the number of alkyl groups attached to a positively charged Cation, greater is the hyperconjugation interaction and stabilization of the cation. In the light of the above statements, choose the correct answer from the options given below

    • A. Statement I is false but Statement II is true
    • B. Statement I is true but Statement II is false
    • C. Both Statement I and Statement II are false
    • D. Both Statement I and Statement II are true
  8. Question 8 · difficulty L2 · understanding

    A species having carbon with sextet of electrons and can act as electrophile is called

    • A. pentavalent carbon
    • B. carbon free radical
    • C. carbanion
    • D. carbocation
  9. Question 9 · difficulty L2 · understanding

    In the following carbocation, H/CH3_3 that is most likely to migrate to the positively charged carbon is :

    • A. CH3_3 at C-4
    • B. H at C-4
    • C. CH3_3 at C-2
    • D. H at C-2
  10. Question 10 · difficulty L2 · understanding

    The total number of contributing structure showing hyper-conjugation (involving C-H bonds) for the following carbocation is _________.

Common mistakes in Electrophiles, nucleophiles and stability of intermediates

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 positively charged species are better electron-pair donors.
  • Confuses the electrophile with a nucleophile or base.
  • Uses steric hindrance alone to rank carbocation stability.
  • Ranks intermediates only by degree of substitution and ignores resonance.

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