MCQMediumJEE 2026Crystal Field Theory

JEE Chemistry 2026 Question with Solution

Given below are two statements :

Statement I : Crystal Field Stabilization Energy (CFSE) of [Cr(H2O)6]2+[Cr(H_2O)_6]^{2+} is greater than that of [Mn(H2O)6]2+[Mn(H_2O)_6]^{2+}.

Statement II : Potassium ferricyanide has a greater spin-only magnetic moment than sodium ferrocyanide.

In the light of the above statements, choose the correct answer from the options given below :

  • A

    Statement I is true but Statement II is false

  • B

    Statement I is false but Statement II is true

  • C

    Both Statement I and Statement II are true

  • D

    Both Statement I and Statement II are false

Answer

Correct answer:C

Step-by-step solution

Standard Method

Given: Two statements about CFSE and spin-only magnetic moment are to be checked.

Find: Which option correctly identifies the truth values of Statement I and Statement II.

For octahedral complexes,

CFSE=[0.4n(t2g)+0.6n(eg)]Δo\text{CFSE} = \left[-0.4\,n(t_{2g}) + 0.6\,n(e_g)\right]\Delta_o

and spin-only magnetic moment depends on the number of unpaired electrons nn:

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

Statement I:

In [Cr(H2O)6]2+[Cr(H_2O)_6]^{2+}, chromium is Cr2+Cr^{2+}, so it is a d4d^4 ion. Since H2OH_2O is a weak field ligand, the complex is high spin.

t2g3eg1t_{2g}^3 e_g^1

Therefore,

CFSE=[3(0.4)+1(0.6)]Δo=0.6Δo\text{CFSE} = \left[3(-0.4) + 1(0.6)\right]\Delta_o = -0.6\Delta_o

In [Mn(H2O)6]2+[Mn(H_2O)_6]^{2+}, manganese is Mn2+Mn^{2+}, so it is a d5d^5 ion. With weak field ligand H2OH_2O, it is also high spin.

t2g3eg2t_{2g}^3 e_g^2

Therefore,

CFSE=[3(0.4)+2(0.6)]Δo=0\text{CFSE} = \left[3(-0.4) + 2(0.6)\right]\Delta_o = 0

The magnitude of CFSE for [Cr(H2O)6]2+[Cr(H_2O)_6]^{2+} is greater than that for [Mn(H2O)6]2+[Mn(H_2O)_6]^{2+}. So Statement I is true.

Statement II:

Potassium ferricyanide is K3[Fe(CN)6]K_3[Fe(CN)_6]. Here iron is in the +3+3 oxidation state, so it is d5d^5. Since CNCN^- is a strong field ligand, the complex is low spin.

t2g5eg0t_{2g}^5 e_g^0

Number of unpaired electrons is n=1n=1.

Sodium ferrocyanide is Na4[Fe(CN)6]Na_4[Fe(CN)_6]. Here iron is in the +2+2 oxidation state, so it is d6d^6. With strong field ligand CNCN^-, the complex is low spin.

t2g6eg0t_{2g}^6 e_g^0

Number of unpaired electrons is n=0n=0.

Since ferricyanide has more unpaired electrons than ferrocyanide, its spin-only magnetic moment is greater. So Statement II is true.

Therefore, both Statement I and Statement II are true. The correct option is C.

Concept Breakdown

Given: Weak field ligand H2OH_2O and strong field ligand CNCN^- are involved.

Find: Compare CFSE values and magnetic moments.

A weak field ligand gives a high spin complex, while a strong field ligand gives a low spin complex.

  1. For [Cr(H2O)6]2+[Cr(H_2O)_6]^{2+}:
  • Cr2+d4Cr^{2+} \to d^4
  • High spin octahedral arrangement: t2g3eg1t_{2g}^3 e_g^1
  • CFSE:
[3(0.4)+1(0.6)]Δo=0.6Δo[3(-0.4) + 1(0.6)]\Delta_o = -0.6\Delta_o
  1. For [Mn(H2O)6]2+[Mn(H_2O)_6]^{2+}:
  • Mn2+d5Mn^{2+} \to d^5
  • High spin octahedral arrangement: t2g3eg2t_{2g}^3 e_g^2
  • CFSE:
[3(0.4)+2(0.6)]Δo=0[3(-0.4) + 2(0.6)]\Delta_o = 0

So, Statement I is true.

  1. For K3[Fe(CN)6]K_3[Fe(CN)_6]:
  • Iron oxidation state =+3= +3
  • Fe3+d5Fe^{3+} \to d^5
  • Strong field, low spin: t2g5eg0t_{2g}^5 e_g^0
  • Unpaired electrons =1=1
  1. For Na4[Fe(CN)6]Na_4[Fe(CN)_6]:
  • Iron oxidation state =+2= +2
  • Fe2+d6Fe^{2+} \to d^6
  • Strong field, low spin: t2g6eg0t_{2g}^6 e_g^0
  • Unpaired electrons =0=0

Hence ferricyanide has greater magnetic moment than ferrocyanide. Statement II is also true.

Therefore, the correct option is C.

Common mistakes

  • Assuming H2OH_2O is a strong field ligand is incorrect because it usually produces high spin octahedral complexes. Use weak-field splitting for [Cr(H2O)6]2+[Cr(H_2O)_6]^{2+} and [Mn(H2O)6]2+[Mn(H_2O)_6]^{2+}.

  • Comparing signed CFSE values without considering magnitude can cause confusion. Here 0.6Δo-0.6\Delta_o represents greater stabilization than 00, so the magnitude of stabilization is larger for the chromium complex.

  • Using the free-ion electron count of iron without first finding oxidation state gives wrong magnetic moments. Determine Fe3+Fe^{3+} in ferricyanide and Fe2+Fe^{2+} in ferrocyanide before writing d5d^5 and d6d^6 configurations.

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