The value for crystal field stabilisation energy is zero for:
(A) ${ K }_{ 2 }\left[ Mn{ F }_{ 6 } \right]$
(B) ${ K }_{ 3 }\left[ Fe(CN)_{ 6 } \right]$
(C) ${ K }_{ 3 }\left[ Fe{ F }_{ 6 } \right]$
(D) ${ K }_{ 4 }\left[ Fe(CN)_{ 6 } \right]$
Answer
249.6k+ views
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 ${ e }_{ g }$ 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 ${ K }_{ 3 }\left[ Fe{ F }_{ 6 } \right]$ is;

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

Atomic number of Fe = ${ 26 }$
Electronic configuration = $\left[ Ar \right] { 3d }^{ 6 }{ 4s }^{ 2 }$
For, ${ Fe }^{ +3 } = \left[ Ar \right] { 3d }^{ 5 } or { t }_{ 2g }^{ 3 }{ e }_{ g }^{ 2 }$
The crystal field splitting energy for octahedral complexes are given by;
CFSE = ${ -0.4\times }{ t }_{ 2g }{ +0.6\times }{ e }_{ g }$
By putting the values, we get
CFSE = ${ -0.4\times 3 }{ +0.6\times 2 }$
CFSE = 0
Now, for ${ K }_{ 2 }\left[ Mn{ F }_{ 6 } \right]$
Atomic number of Mn = ${ 25 }$
Electronic configuration = $\left[ Ar \right] { 3d }^{ 5 }{ 4s }^{ 2 }$
For, ${ Mn }^{ +3 } = \left[ Ar \right] { 3d }^{ 4 }or { t }_{ 2g }^{ 3 }{ e }_{ g }^{ 1 }$
The crystal field splitting energy for octahedral complexes are given by;
CFSE = ${ -0.4\times }{ t }_{ 2g }{ +0.6\times }{ e }_{ g }$
By putting the values, we get
CFSE = ${ -0.4\times 3 }{ +0.6\times 1 }$
CFSE = ${ -0.6 } \Delta _{ 0 }$
Hence, we can say that the value for crystal field stabilization energy is zero for ${ K }_{ 3 }\left[ Fe{ F }_{ 6 } \right]$.
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.
Recently Updated Pages
JEE Isolation, Preparation and Properties of Non-metals Important Concepts and Tips for Exam Preparation

Isoelectronic Definition in Chemistry: Meaning, Examples & Trends

Ionisation Energy and Ionisation Potential Explained

Iodoform Reactions - Important Concepts and Tips for JEE

Introduction to Dimensions: Understanding the Basics

Instantaneous Velocity Explained: Formula, Examples & Graphs

Trending doubts
JEE Main 2026: Exam Dates, Session 2 Updates, City Slip, Admit Card & Latest News

Hybridisation in Chemistry – Concept, Types & Applications

JEE Main 2026 Application Login: Direct Link, Registration, Form Fill, and Steps

Understanding the Electric Field of a Uniformly Charged Ring

Derivation of Equation of Trajectory Explained for Students

JEE Main Marking Scheme 2026- Paper-Wise Marks Distribution and Negative Marking Details

Other Pages
CBSE Class 12 Chemistry Question Paper 2026 PDF Download (All Sets) with Answer Key

NCERT Solutions For Class 12 Chemistry Chapter 10 Biomolecules - 2025-26

JEE Advanced Marks vs Ranks 2025: Understanding Category-wise Qualifying Marks and Previous Year Cut-offs

NCERT Solutions For Class 12 Chemistry Chapter 2 Electrochemistry - 2025-26

NCERT Solutions For Class 12 Chemistry Chapter 1 Solutions - 2025-26

NCERT Solutions For Class 12 Chemistry Chapter 3 Chemical Kinetics - 2025-26

