JEE Challenger
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Determine Spin Only Magnetic Moments of Chromium and Copper Complexes

Calculate the spin-only magnetic moments (in BM\text{BM}) for [Cr(NH3)6]3+[\text{Cr(NH}_3)_6]^{3+} and [CuF6]3−[\text{CuF}_6]^{3-}, respectively. (Note: The atomic numbers of Cr\text{Cr} and Cu\text{Cu} are 2424 and 2929, respectively)

Options

A

3.873.87 and 2.842.84

Correct
B

4.904.90 and 1.731.73

C

3.873.87 and 1.731.73

D

4.904.90 and 2.842.84

Step-by-Step Solution

To determine the spin-only magnetic moments of the given coordination complexes, we calculate the number of unpaired electrons (nn) present in the central metal ion of each complex using Crystal Field Theory (CFT).


1. Complex 1: [Cr(NH3)6]3+[\text{Cr(NH}_3)_6]^{3+}

  • Oxidation State of Chromium (Cr\text{Cr}): Let the oxidation state of Cr\text{Cr} be xx. Since NH3\text{NH}_3 is a neutral ligand: x+6(0)=+3  ⟹  x=+3x + 6(0) = +3 \implies x = +3 Thus, the central metal ion is Cr3+\text{Cr}^{3+}.

  • Electronic Configuration:

    • Ground state configuration of Cr\text{Cr} (Z=24Z = 24): [Ar] 3d54s1[\text{Ar}] \, 3d^5 4s^1
    • Configuration of Cr3+\text{Cr}^{3+}: [Ar] 3d3[\text{Ar}] \, 3d^3
  • Crystal Field Splitting in Octahedral Field: For a d3d^3 metal ion in an octahedral complex, the three electrons enter the lower energy t2gt_{2g} orbitals according to Hund's rule: Electronic configuration=t2g3 eg0\text{Electronic configuration} = t_{2g}^3 \, e_g^0

    • Number of unpaired electrons, n=3n = 3.
  • Spin-Only Magnetic Moment (μs.o.\mu_{\text{s.o.}}): μs.o.=n(n+2) BM\mu_{\text{s.o.}} = \sqrt{n(n + 2)} \text{ BM} μs.o.=3(3+2)=15≈3.87 BM\mu_{\text{s.o.}} = \sqrt{3(3 + 2)} = \sqrt{15} \approx 3.87 \text{ BM}


2. Complex 2: [CuF6]3−[\text{CuF}_6]^{3-}

  • Oxidation State of Copper (Cu\text{Cu}): Let the oxidation state of Cu\text{Cu} be yy. Since F−\text{F}^- has a charge of −1-1: y+6(−1)=−3  ⟹  y=+3y + 6(-1) = -3 \implies y = +3 Thus, the central metal ion is Cu3+\text{Cu}^{3+}.

  • Electronic Configuration:

    • Ground state configuration of Cu\text{Cu} (Z=29Z = 29): [Ar] 3d104s1[\text{Ar}] \, 3d^{10} 4s^1
    • Configuration of Cu3+\text{Cu}^{3+}: [Ar] 3d8[\text{Ar}] \, 3d^8
  • Crystal Field Splitting in Octahedral Field: For a d8d^8 metal ion in an octahedral complex, the distribution of 8 electrons between t2gt_{2g} and ege_g orbitals is fixed regardless of ligand strength: Electronic configuration=t2g6 eg2\text{Electronic configuration} = t_{2g}^6 \, e_g^2

    • The t2gt_{2g} set is completely filled (6 paired electrons).
    • The ege_g set contains 2 electrons which occupy the degenerate dx2−y2d_{x^2-y^2} and dz2d_{z^2} orbitals singly.
    • Number of unpaired electrons, n=2n = 2.
  • Spin-Only Magnetic Moment (μs.o.\mu_{\text{s.o.}}): μs.o.=n(n+2) BM\mu_{\text{s.o.}} = \sqrt{n(n + 2)} \text{ BM} μs.o.=2(2+2)=8≈2.84 BM\mu_{\text{s.o.}} = \sqrt{2(2 + 2)} = \sqrt{8} \approx 2.84 \text{ BM}


Conclusion:

The calculated spin-only magnetic moments of [Cr(NH3)6]3+[\text{Cr(NH}_3)_6]^{3+} and [CuF6]3−[\text{CuF}_6]^{3-} are 3.87 BM3.87 \text{ BM} and 2.84 BM2.84 \text{ BM}, respectively.

This matches Option (A).