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Coordination Compounds question

2020 · 2 Sep · Shift 1 · Q12
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Coordination Compounds question

2020 · 2 Sep · Shift 1 · Q12

JEE MainChemistryCoordination CompoundsMCQ+4 / −1
Consider that a d6 metal ion (M2+M^{2+}M2+) forms a complex with aqua ligands, and the spin only magnetic moment of the complex is 4.90 BM. The geometry and the crystal field stabilization energy of the complex is
  1. A
    tetrahedral and – 1.6 Δ\DeltaΔ t + 1P
  2. B
    octahedral and –2.4 Δ\DeltaΔ 0 + 2P
  3. C
    tetrahedral and –0.6 Δ\DeltaΔ t
  4. D
    octahedral and –1.6 Δ\DeltaΔ 0
View written solutionFree

Correct answer: C

  1. Find the number of unpaired electrons from magnetic moment

For spin-only magnetic moment,

μ=n(n+2) BM\mu = \sqrt{n(n+2)}\ \text{BM}μ=n(n+2)​ BM

where nnn is the number of unpaired electrons.

Given:

μ=4.90 BM\mu = 4.90\ \text{BM}μ=4.90 BM

Now check:

4(4+2)=24≈4.90\sqrt{4(4+2)} = \sqrt{24} \approx 4.904(4+2)​=24​≈4.90

So, the complex has

n=4n=4n=4

unpaired electrons.


  1. Electronic configuration of a d6d^6d6 ion

The metal ion is d6d^6d6.

We need a geometry that gives 4 unpaired electrons.


  1. Check octahedral case

For octahedral splitting:

  • Lower set: t2gt_{2g}t2g​
  • Upper set: ege_geg​

For a d6d^6d6 ion:

  • High spin octahedral: t2g4eg2t_{2g}^4 e_g^2t2g4​eg2​ → 4 unpaired electrons
  • Low spin octahedral: t2g6eg0t_{2g}^6 e_g^0t2g6​eg0​ → 0 unpaired electrons

Since aqua is a weak field ligand, the octahedral aqua complex would be high spin. Thus configuration is:

t2g4eg2t_{2g}^4 e_g^2t2g4​eg2​

which indeed has 4 unpaired electrons.

Now compute CFSE:

  • each t2gt_{2g}t2g​ electron contributes −0.4Δo-0.4\Delta_o−0.4Δo​
  • each ege_geg​ electron contributes +0.6Δo+0.6\Delta_o+0.6Δo​

So,

CFSE=4(−0.4Δo)+2(+0.6Δo)\text{CFSE} = 4(-0.4\Delta_o) + 2(+0.6\Delta_o)CFSE=4(−0.4Δo​)+2(+0.6Δo​) =−1.6Δo+1.2Δo= -1.6\Delta_o + 1.2\Delta_o=−1.6Δo​+1.2Δo​ =−0.4Δo= -0.4\Delta_o=−0.4Δo​

There is one paired electron pair, so pairing contribution is

+P+P+P

Hence total:

CFSE=−0.4Δo+P\text{CFSE} = -0.4\Delta_o + PCFSE=−0.4Δo​+P

This does not match option B or D.


  1. Check tetrahedral case

For tetrahedral splitting:

  • Lower set: eee
  • Upper set: t2t_2t2​

Tetrahedral complexes are almost always high spin. For d6d^6d6 tetrahedral configuration:

e3t23e^3 t_2^3e3t23​

This gives 4 unpaired electrons, consistent with the magnetic moment.

Now compute CFSE in tetrahedral field:

  • each eee electron contributes −0.6Δt-0.6\Delta_t−0.6Δt​
  • each t2t_2t2​ electron contributes +0.4Δt+0.4\Delta_t+0.4Δt​

Thus,

CFSE=3(−0.6Δt)+3(+0.4Δt)\text{CFSE} = 3(-0.6\Delta_t) + 3(+0.4\Delta_t)CFSE=3(−0.6Δt​)+3(+0.4Δt​) =−1.8Δt+1.2Δt= -1.8\Delta_t + 1.2\Delta_t=−1.8Δt​+1.2Δt​ =−0.6Δt= -0.6\Delta_t=−0.6Δt​

There is one paired electron in e3e^3e3, but CFSE option is usually written separately unless pairing energy is explicitly added. So the correct matching expression is:

−0.6Δt-0.6\Delta_t−0.6Δt​

This matches Option C.


  1. Evaluate options
  • A: tetrahedral and −1.6Δt+1P-1.6\Delta_t + 1P−1.6Δt​+1P ❌ Incorrect CFSE
  • B: octahedral and −2.4Δo+2P-2.4\Delta_o + 2P−2.4Δo​+2P ❌ Incorrect for d6d^6d6 high-spin aqua complex
  • C: tetrahedral and −0.6Δt-0.6\Delta_t−0.6Δt​ ✅ Correct
  • D: octahedral and −1.6Δo-1.6\Delta_o−1.6Δo​ ❌ Incorrect CFSE

  1. Final answer

The complex is tetrahedral with CFSE

−0.6Δt-0.6\Delta_t−0.6Δt​

So the correct option is C.

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