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Coordination Compounds question

2015 · Shift 1 · Q12
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Coordination Compounds question

2015 · Shift 1 · Q12

JEE AdvancedChemistryCoordination CompoundsNumerical+3 / −1
For the octahedral complexes of Fe3+{}^{3+}3+ in SCN −-− (thiocyana-to-S) and in CN −-− ligand environments, the difference between the spin-only magnetic moments in Bohr magnetons (when approximated to the nearest integer) is ‾\underline{\hspace{2cm}}​. [Atomic number Fe = 26]
Numerical answer
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Correct answer: 4

  1. Find the electronic configuration of Fe3+\mathrm{Fe^{3+}}Fe3+

Fe has atomic number 262626.

Fe:[Ar]3d64s2\mathrm{Fe}: [Ar]3d^6 4s^2Fe:[Ar]3d64s2

For Fe3+\mathrm{Fe^{3+}}Fe3+, remove two 4s4s4s electrons and one 3d3d3d electron:

Fe3+:[Ar]3d5\mathrm{Fe^{3+}}: [Ar]3d^5Fe3+:[Ar]3d5

So, Fe3+\mathrm{Fe^{3+}}Fe3+ is a d5d^5d5 ion.

  1. Case 1: SCN−^-− (thiocyanato-S) ligand environment

SCN−^-− coordinated through sulfur is a weak field ligand. In an octahedral field, a weak field ligand gives a high-spin configuration.

For octahedral high-spin d5d^5d5:

t2g3eg2t_{2g}^3 e_g^2t2g3​eg2​

Number of unpaired electrons:

n=5n = 5n=5

Spin-only magnetic moment:

μ=n(n+2)=5(5+2)=35≈5.92 BM\mu = \sqrt{n(n+2)} = \sqrt{5(5+2)} = \sqrt{35} \approx 5.92\ \text{BM}μ=n(n+2)​=5(5+2)​=35​≈5.92 BM

Approximated to nearest integer:

μ≈6 BM\mu \approx 6\ \text{BM}μ≈6 BM

  1. Case 2: CN−^-− ligand environment

CN−^-− is a strong field ligand. In an octahedral field, it gives a low-spin configuration.

For octahedral low-spin d5d^5d5:

t2g5eg0t_{2g}^5 e_g^0t2g5​eg0​

Number of unpaired electrons:

n=1n = 1n=1

Spin-only magnetic moment:

μ=1(1+2)=3≈1.73 BM\mu = \sqrt{1(1+2)} = \sqrt{3} \approx 1.73\ \text{BM}μ=1(1+2)​=3​≈1.73 BM

Approximated to nearest integer:

μ≈2 BM\mu \approx 2\ \text{BM}μ≈2 BM

  1. Find the required difference

6−2=46 - 2 = 46−2=4

So, the difference between the spin-only magnetic moments is

4\boxed{4}4​

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