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Question: The value for crystal field stabilisation energy is zero for: (A) \({ K }_{ 2 }\left[ Mn{ F }_{ 6 ...

The value for crystal field stabilisation energy is zero for:
(A) K2[MnF6]{ K }_{ 2 }\left[ Mn{ F }_{ 6 } \right]
(B) K3[Fe(CN)6]{ K }_{ 3 }\left[ Fe(CN)_{ 6 } \right]
(C) K3[FeF6]{ K }_{ 3 }\left[ Fe{ F }_{ 6 } \right]
(D) K4[Fe(CN)6]{ K }_{ 4 }\left[ Fe(CN)_{ 6 } \right]

Explanation

Solution

Hint: Crystal field stabilization energy: Crystal field stabilization energy is the energy of electronic configuration in the ligand field - Electronic configuration in the isotropic field.

Complete answer step-by-step:

The splitting pattern in each complex compound is octahedral. If a strong field ligand is present, then back pairing will take place as in the case of B and D, and splitting energy can never be zero, since no electron can go into eg{ e }_{ g } orbitals.
But if a strong field is not present, then back pairing will not take place as in the case of A and C.
The splitting pattern in K3[FeF6]{ K }_{ 3 }\left[ Fe{ F }_{ 6 } \right] is;

Atomic number of Fe = 26{ 26 }
Electronic configuration = [Ar]3d64s2\left[ Ar \right] { 3d }^{ 6 }{ 4s }^{ 2 }
For, Fe+3=[Ar]3d5ort2g3eg2{ Fe }^{ +3 } = \left[ Ar \right] { 3d }^{ 5 } or { t }_{ 2g }^{ 3 }{ e }_{ g }^{ 2 }
The crystal field splitting energy for octahedral complexes are given by;
CFSE = 0.4×t2g+0.6×eg{ -0.4\times }{ t }_{ 2g }{ +0.6\times }{ e }_{ g }
By putting the values, we get
CFSE = 0.4×3+0.6×2{ -0.4\times 3 }{ +0.6\times 2 }
CFSE = 0
Now, for K2[MnF6]{ K }_{ 2 }\left[ Mn{ F }_{ 6 } \right]
Atomic number of Mn = 25{ 25 }
Electronic configuration = [Ar]3d54s2\left[ Ar \right] { 3d }^{ 5 }{ 4s }^{ 2 }
For, Mn+3=[Ar]3d4ort2g3eg1{ Mn }^{ +3 } = \left[ Ar \right] { 3d }^{ 4 }or { t }_{ 2g }^{ 3 }{ e }_{ g }^{ 1 }
The crystal field splitting energy for octahedral complexes are given by;
CFSE = 0.4×t2g+0.6×eg{ -0.4\times }{ t }_{ 2g }{ +0.6\times }{ e }_{ g }
By putting the values, we get
CFSE = 0.4×3+0.6×1{ -0.4\times 3 }{ +0.6\times 1 }
CFSE = 0.6Δ0{ -0.6 } \Delta _{ 0 }
Hence, we can say that the value for crystal field stabilization energy is zero for K3[FeF6]{ K }_{ 3 }\left[ Fe{ F }_{ 6 } \right].
The correct option is C.

Note: The possibility to make a mistake is that you may use the crystal field splitting energy formula for tetrahedral, not octahedral. But all the compounds are octahedral so do not confuse between them.