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NEET-UG and JEE Main Chemistry · Class 12

Valence bond theory and crystal field theory — NEET & JEE Questions

Valence bond theory and crystal field theory is a topic in Coordination Compounds, a Class 12 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 133 published NEET-UG and JEE Main questions on Valence bond theory and crystal field theory, each with the marking scheme of the real paper.

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Valence bond theory and crystal field theory MCQs with solutions

10 of the 133 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

    Crystal field theory explains splitting of d-orbital energies mainly through

    • A. electrostatic interaction between metal ions and surrounding ligands
    • B. nuclear fission
    • C. hydrogen bonding between ligands only
    • D. complete electron transfer to ligands
  2. Question 2 · difficulty L2 · understanding

    The ratio of spin-only magnetic moment values μeff [Cr(CN)6]3−/μeff [Cr(H2O)6]3+\mu_{\text {eff }}\left[\mathrm{Cr}(\mathrm{CN})_{6}\right]^{3-} / \mu_{\text {eff }}\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+} is _________.

  3. Question 3 · difficulty L2 · understanding

    For a metal ion, the calculated magnetic moment is 4.90 BM4.90 ~\mathrm{BM}. This metal ion has ___________ number of unpaired electrons.

  4. Question 4 · difficulty L2 · understanding

    [Ti(H 2 O) 6 ] 3+ absorbs light of wavelength 498 nm during a d −- d transition. The octahedral splitting energy for the above complex is ____________ ×\times 10 −-19 J. (Round off to the Nearest Integer). h = 6.626 ×\times 10 −-34 Js; c = 3 ×\times 10 8 ms −-1

  5. Question 5 · difficulty L2 · understanding

    Given below are two statements: Statement I: Each electron in eg\mathrm{e}_{\mathrm{g}} orbitals destabilizes the orbitals by +0.6Δo+0.6 \Delta_{\mathrm{o}} and each electron in the t2gt_{2 g} orbitals stabilizes the orbitals by −0.4Δ0-0.4 \Delta_0 in an octahedral field on the basis of crystal field theory. Statement II: All the d - orbitals of the transition metals have the same energy in their free atomic state but when a complex is formed the ligands destroy the degeneracy of these orbitals on the basis of crystal field theory. 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
  6. Question 6 · difficulty L2 · understanding

     Match the LIST-I with LIST-II  \text { Match the LIST-I with LIST-II } List-I Complex ion List-II Calculated spin only magnetic moment (BM) A. [Cr(H2O)6]2+ \left[\mathrm{Cr}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+} I. 3.87 B. [Co(H2O)6]2+ \left[\mathrm{Co}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+} II. 5.92 C. [Cu(H2O)6]2+ \left[\mathrm{Cu}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+} III. 4.90 D. [Mn(H2O)6]2+ \left[\mathrm{Mn}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+} IV. 1.73 Choose the correct answer from the options given below :

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

    Match List - I with List - II. List - I Chromium (III) Complexes (en = ethylene diamine) List - II Δ₀ (cm⁻¹) A [Cr(CN)₆]³⁻ I. 15,060 B [CrF₆]³⁻ II. 17,400 C [Cr(H₂O)₆]³⁺ III. 22,300 D [Cr(en)₃]³⁺ IV. 26,600 Choose the correct answer from the options given below:

    • A. A-I, B-II, C-III, D-IV
    • B. A-II, B-III, C-IV, D-I
    • C. A-III, B-IV, C-I, D-II
    • D. A-IV, B-I, C-II, D-III
  8. Question 8 · difficulty L2 · understanding

     Match the LIST-I with LIST-II  \text { Match the LIST-I with LIST-II } LIST-I (Molecules/ion) LIST-II (Hybridisation of central atom) A. PF5 \mathrm{PF}_5 I dsp2 \mathrm{dsp}^2 B SF6 \mathrm{SF}_6 II sp3 d \mathrm{sp}^3 \mathrm{~d} C Ni(CO)4 \mathrm{Ni}(\mathrm{CO})_4 III sp3 d2 \mathrm{sp}^3 \mathrm{~d}^2 D [PtCl4]2− \left[\mathrm{PtCl}_4\right]^{2-} IV sp3 \mathrm{sp}^3  Choose the correct answer from the options given below:  \text { Choose the correct answer from the options given below: }

    • A. A-IV, B-I, C-II, D-III
    • B. A-III, B-I, C-IV, D-II
    • C. A-II, B-III, C-IV, D-I
    • D. A-I, B-II, C-III, D-IV
  9. Question 9 · difficulty L2 · understanding

    Given below are two statements : Statement (I) : In octahedral complexes, when Δ0<P\Delta_0<\mathrm{P} high spin complexes are formed. When Δ0>P\Delta_0>P low spin complexes are formed. Statement (II) : In tetrahedral complexes because of Δt<P\Delta_t < P, low spin complexes are rarely formed. In the light of the above statements, choose the most appropriate answer from the options given below :

    • A. Both Statement I and Statement II are incorrect
    • B. Statement I is correct but Statement II is incorrect
    • C. Statement I is incorrect but Statement II is correct
    • D. Both Statement I and Statement II are correct
  10. Question 10 · difficulty L2 · understanding

    The correct order of ligands arranged in increasing field strength.

    • A. F−<Br−<I−<NH3\mathrm{F}^{-}<\mathrm{Br}^{-}<\mathrm{I}^{-}<\mathrm{NH}_3
    • B. H2O<−OH<CN−<NH3\mathrm{H}_2 \mathrm{O}<\mathrm{^{-}OH}<\mathrm{CN}^{-}<\mathrm{NH}_3
    • C. Br−<F−<H2O<NH3\mathrm{Br}^{-}<\mathrm{F}^{-}<\mathrm{H}_2 \mathrm{O}<\mathrm{NH}_3
    • D. Cl−<−OH<Br−<CN−\mathrm{Cl}^{-}<\mathrm{^{-}OH}<\mathrm{Br}^{-}<\mathrm{CN}^{-}

Common mistakes in Valence bond theory and crystal field theory

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.

  • Ignores the competition between crystal-field splitting and pairing energy.

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