MCQEasyJEE 2023Crystal Field Theory

JEE Chemistry 2023 Question with Solution

The magnetic moment is measured in Bohr Magneton (BM\text{BM}). Spin only magnetic moment of Fe in [Fe(H2O)6]3+[Fe(H_2O)_6]^{3+} and [Fe(CN)6]3[Fe(CN)_6]^{3-} complexes respectively is:

  • A

    3.873.87 B.M. and 1.7321.732 B.M.

  • B

    6.926.92 B.M. in both

  • C

    5.925.92 B.M. and 1.7321.732 B.M.

  • D

    4.894.89 B.M. and 6.926.92 B.M.

Answer

Correct answer:C

Step-by-step solution

Standard Method

Given: The complexes are [Fe(H2O)6]3+[Fe(H_2O)_6]^{3+} and [Fe(CN)6]3[Fe(CN)_6]^{3-}.

Find: The spin only magnetic moments of Fe in both complexes.

For Fe3+Fe^{3+}, the electronic configuration is [Ar]3d5[Ar]3d^5.

In [Fe(H2O)6]3+[Fe(H_2O)_6]^{3+}, H2OH_2O is a weak field ligand, so no pairing occurs. Hence the number of unpaired electrons is n=5n=5.

The spin-only magnetic moment is

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

Substituting n=5n=5,

μ=5(5+2)=355.92BM\mu = \sqrt{5(5+2)} = \sqrt{35} \approx 5.92 \, \text{BM}

In [Fe(CN)6]3[Fe(CN)_6]^{3-}, CNCN^- is a strong field ligand, so pairing occurs. Hence the number of unpaired electrons is n=1n=1.

Again using

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

Substituting n=1n=1,

μ=1(1+2)=31.732BM\mu = \sqrt{1(1+2)} = \sqrt{3} \approx 1.732 \, \text{BM}

Therefore, the spin-only magnetic moments are 5.92BM5.92 \, \text{BM} and 1.732BM1.732 \, \text{BM} respectively. The correct option is C.

Electron Configuration Explanation

Given: Both complexes contain Fe3+Fe^{3+}.

Find: How ligand strength changes the number of unpaired electrons and hence the magnetic moment.

Neutral Fe has configuration [Ar]3d64s2[Ar]3d^64s^2. Removing three electrons gives

Fe3+:[Ar]3d5Fe^{3+} : [Ar]3d^5

For [Fe(H2O)6]3+[Fe(H_2O)_6]^{3+}, H2OH_2O is a weak field ligand, so the complex is high spin. Thus all five 3d3d electrons remain unpaired.

For [Fe(CN)6]3[Fe(CN)_6]^{3-}, CNCN^- is a strong field ligand, so the complex is low spin. The electrons pair as much as possible, leaving only one unpaired electron.

Now apply

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

For the first complex, n=5n=5 gives μ5.92BM\mu \approx 5.92 \, \text{BM}. For the second complex, n=1n=1 gives μ1.732BM\mu \approx 1.732 \, \text{BM}.

Hence the correct choice is C. The solution says option A, but its worked values clearly match option C. Therefore the worked solution determines the answer.

Common mistakes

  • Assuming both complexes have the same magnetic moment because Fe is in the +3+3 oxidation state in both is incorrect. Ligand strength changes the number of unpaired electrons. Always determine whether the ligand is weak field or strong field before counting unpaired electrons.

  • Using the neutral Fe configuration instead of Fe3+Fe^{3+} is wrong. First remove electrons to get Fe3+:[Ar]3d5Fe^{3+} : [Ar]3d^5, then analyze the crystal field splitting.

  • Treating H2OH_2O as a strong field ligand or CNCN^- as a weak field ligand gives the wrong spin state. Remember that H2OH_2O usually forms a high-spin complex, while CNCN^- usually forms a low-spin complex.

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