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Question #44582

Difficulty: 8/10 | 🟢 Free

The Question

Consider the following three octahedral complexes at 298 K: P=\ce[Cr(H2O)6]3+P = \ce{[Cr(H2O)6]^{3+}} Q=\ce[Fe(CN)6]3−Q = \ce{[Fe(CN)6]^{3-}} R=\ce[Ni(en)3]2+R = \ce{[Ni(en)3]^{2+}} (where \ceen=ethylenediamine\ce{en} = \text{ethylenediamine})

A common, yet flawed, heuristic derived from a simplified Valence Bond Theory (VBT) states: 'Strong-field ligands always force spin-pairing to form inner-orbital (d2sp3d^2sp^3) complexes, while weak-field ligands always result in outer-orbital (sp3d2sp^3d^2) complexes.'

Which of the following correctly identifies the actual hybridization and spin-only magnetic moment (μeff\mu_{eff}) for PP, QQ, and RR, thereby demonstrating the limitations of this heuristic?

Options

  • A.

    PP: d2sp3d^2sp^3, 3.87 BM∣Q3.87\text{ BM} \mid Q: d2sp3d^2sp^3, 1.73 BM∣R1.73\text{ BM} \mid R: sp3d2sp^3d^2, 2.83 BM2.83\text{ BM}

  • B.

    PP: sp3d2sp^3d^2, 3.87 BM∣Q3.87\text{ BM} \mid Q: d2sp3d^2sp^3, 1.73 BM∣R1.73\text{ BM} \mid R: d2sp3d^2sp^3, 0.00 BM0.00\text{ BM}

  • C.

    PP: sp3d2sp^3d^2, 3.87 BM∣Q3.87\text{ BM} \mid Q: sp3d2sp^3d^2, 5.92 BM∣R5.92\text{ BM} \mid R: d2sp3d^2sp^3, 2.83 BM2.83\text{ BM}

  • D.

    PP: d2sp3d^2sp^3, 3.87 BM∣Q3.87\text{ BM} \mid Q: sp3d2sp^3d^2, 5.92 BM∣R5.92\text{ BM} \mid R: sp3d2sp^3d^2, 2.83 BM2.83\text{ BM}

Check Your Answer

Correct Answer

Step-by-Step Solution

Explanation

How the Examiner Thinks

Exception_Exposure

Learn to identify edge cases and boundary exceptions that JEE examiners hide in math problems.

Concepts Behind This Question

Valence Bond Theory Hybridization|Spin-Only Magnetic Moment|Crystal Field Splitting (Octahedral)

Why This Question Is Tricky

Common Mistakes

The question tests the fundamental limitation of Valence Bond Theory (VBT) and the common student misconception that 'strong-field ligands always form inner-orbital complexes' and 'weak-field ligands always form outer-orbital complexes.' By selecting d3d^3 (\ceCr3+\ce{Cr^{3+}}) and d8d^8 (\ceNi2+\ce{Ni^{2+}}) systems, the problem exposes that for these specific electronic configurations, the availability of inner dd-orbitals dictates the hybridization (d2sp3d^2sp^3 for d3d^3, sp3d2sp^3d^2 for d8d^8), completely independent of the spectrochemical series.

The d5d^5 system (\ceFe3+\ce{Fe^{3+}}) acts as a control where the heuristic actually works, further trapping students who apply the rule blindly across all options.

Quick Facts About This Question

Question Information

SubjectChemistry
ChapterCoordination Compounds - Class 12
ConceptValence Bond Theory Hybridization
Difficulty8
Cognitive Load7
Target Solve Time160 sec
AccessFree