MCQEasyJEE 2024Crystal Field Theory

JEE Chemistry 2024 Question with Solution

Consider the following complex ions: P = [FeF6]3[FeF_6]^{3-} Q = [V(H2O)6]2+[V(H_2O)_6]^{2+} R = [Fe(H2O)6]2+[Fe(H_2O)_6]^{2+} The correct order of the complex ions, according to their spin-only magnetic moment values (in B.M.), is:

  • A

    R < Q < P

  • B

    R < P < Q

  • C

    Q < R < P

  • D

    Q < P < R

Answer

Correct answer:C

Step-by-step solution

Standard Method

Given: The complex ions are P=[FeF6]3P = [FeF_6]^{3-}, Q=[V(H2O)6]2+Q = [V(H_2O)_6]^{2+}, and R=[Fe(H2O)6]2+R = [Fe(H_2O)_6]^{2+}.

Find: The correct increasing order of their spin-only magnetic moments.

The spin-only magnetic moment is given by

μs=n(n+2)\mu_s = \sqrt{n(n+2)}

where nn is the number of unpaired electrons.

For P=[FeF6]3P = [FeF_6]^{3-}: iron is in the +3+3 oxidation state, so it is Fe3+=3d5Fe^{3+} = 3d^5. Since FF^- is a weak field ligand, the complex is high spin and all 55 electrons remain unpaired.

μs=5(5+2)=355.92B.M.\mu_s = \sqrt{5(5+2)} = \sqrt{35} \approx 5.92 \, \text{B.M.}

For Q=[V(H2O)6]2+Q = [V(H_2O)_6]^{2+}: vanadium is in the +2+2 oxidation state, so it is V2+=3d3V^{2+} = 3d^3. Water is a weak field ligand, so there are 33 unpaired electrons.

μs=3(3+2)=153.87B.M.\mu_s = \sqrt{3(3+2)} = \sqrt{15} \approx 3.87 \, \text{B.M.}

For R=[Fe(H2O)6]2+R = [Fe(H_2O)_6]^{2+}: iron is in the +2+2 oxidation state, so it is Fe2+=3d6Fe^{2+} = 3d^6. Water is a weak field ligand, so the complex is high spin with 44 unpaired electrons.

μs=4(4+2)=244.90B.M.\mu_s = \sqrt{4(4+2)} = \sqrt{24} \approx 4.90 \, \text{B.M.}

Therefore, the order of magnetic moments is Q<R<PQ < R < P.

The correct option is C.

Common mistakes

  • Treating H2OH_2O as a strong field ligand is incorrect here. In these octahedral complexes, H2OH_2O usually gives high-spin configurations for V2+V^{2+} and Fe2+Fe^{2+}. First determine whether the ligand is weak or strong field before counting unpaired electrons.

  • Using the wrong oxidation state for the metal leads to an incorrect dd-electron count. Always calculate the oxidation state from the overall charge of the complex, then write the correct electronic configuration of the metal ion.

  • Comparing magnetic moments without counting unpaired electrons is risky. The formula depends on nn, the number of unpaired electrons, not directly on the atomic number. Find nn first, then use μs=n(n+2)\mu_s = \sqrt{n(n+2)}.

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