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CFSE for d^(6) octahedral complex having...

`CFSE` for `d^(6)` octahedral complex having `Delta =250` and `P =125kJmo1^(-1)` is .

A

`350KJMO1^(-1)`

B

`-350kJmo1^(-1)`

C

`475kJmo1^(-1)`

D

`-475kJmo1^(-1)`

Text Solution

AI Generated Solution

The correct Answer is:
To calculate the Crystal Field Stabilization Energy (CFSE) for a \(d^6\) octahedral complex with a given \(\Delta\) and pairing energy \(P\), we can follow these steps: ### Step 1: Identify the given values - \(d^6\) configuration - \(\Delta = 250 \, \text{kJ/mol}\) - \(P = 125 \, \text{kJ/mol}\) ### Step 2: Determine the type of ligand Since \(\Delta\) (250 kJ/mol) is greater than \(P\) (125 kJ/mol), pairing of electrons will occur. This indicates that the complex is likely to be a strong field ligand. ### Step 3: Fill the d-orbitals In a strong field ligand scenario for a \(d^6\) configuration: - The electrons will fill the \(t_{2g}\) orbitals first and then pair up in the \(t_{2g}\) before filling the \(e_g\) orbitals. - The filling will be as follows: - \(t_{2g}\): 6 electrons (3 pairs) - \(e_g\): 0 electrons ### Step 4: Calculate the CFSE The CFSE can be calculated using the formula: \[ \text{CFSE} = (n_{t_{2g}} \times -0.4\Delta) + (n_{e_g} \times +0.6\Delta) - \text{Pairing Energy} \] Where: - \(n_{t_{2g}} = 6\) (number of electrons in \(t_{2g}\)) - \(n_{e_g} = 0\) (number of electrons in \(e_g\)) ### Step 5: Substitute the values Substituting the values into the CFSE formula: \[ \text{CFSE} = (6 \times -0.4 \times 250) + (0 \times 0.6 \times 250) - \text{Pairing Energy} \] \[ \text{CFSE} = (6 \times -100) + 0 - (2 \times 125) \] \[ \text{CFSE} = -600 - 250 \] \[ \text{CFSE} = -850 \, \text{kJ/mol} \] ### Step 6: Final calculation Since we need to consider the pairing energy for the two paired electrons: \[ \text{Total CFSE} = -600 + 250 = -350 \, \text{kJ/mol} \] ### Conclusion The CFSE for the \(d^6\) octahedral complex is: \[ \text{CFSE} = -350 \, \text{kJ/mol} \]

To calculate the Crystal Field Stabilization Energy (CFSE) for a \(d^6\) octahedral complex with a given \(\Delta\) and pairing energy \(P\), we can follow these steps: ### Step 1: Identify the given values - \(d^6\) configuration - \(\Delta = 250 \, \text{kJ/mol}\) - \(P = 125 \, \text{kJ/mol}\) ### Step 2: Determine the type of ligand ...
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Crystal field splitting energey (CFSE) for the complex [Fe(O)_(4)]^(2-) is when Delta =125 and P =250kJmo1^(-1) .

Determine the crystal field stabilisation energy of a d^(6) complex having Delta_(0) = 25000cm^(-1) and P =1500cm^(-1) .

Magnetic moment (spin only) of octahedron complex having CFSE=- 0.8Delta_(0) and surrounded by weak field ligands can be:

Crystal field splitting energy (CFSE) for the complex [Cr(NH_(3))_(6)]^(2+) is when P =125 and Delta_(0) =250kjmol^(-1) .

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: Value of CFSE depends upon nature of ligand and a spectrochemical series has been made experimentally, for tetrahedral complexes, Delta is about 4/9 times to Delta_(0) (CFSE for octahedral complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. For an octahedral complex, which of the followin d-electron configuration will give maximum CFSE?

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: Value of CFSE depends upon nature of ligand and a spectrochemical series has been made experimentally, for tetrahedral complexes, Delta is about 4/9 times to Delta_(0) (CFSE for octahedral complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. The extent of crystal field splitting in octahedral complexes of the given metal with particular weak field ligand are:

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: Value of CFSE depends upon nature of ligand and a spectrochemical series has been made experimentally, for tetrahedral complexes, Delta is about 4/9 times to Delta_(0) (CFSE for octahedral complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. The d-orbitals, which are stabillized in an octahedral magnetic field, are:

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: Value of CFSE depends upon nature of ligand and a spectrochemical series has been made experimentally, for tetrahedral complexes, Delta is about 4/9 times to Delta_(0) (CFSE for octahedral complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. Cr^(3+) form four complexes with four different ligands which are [Cr(Cl)_(6)]^(3-), [Cr(H_(2)O)_(6)]^(3+) , [Cr(NH_(3))_(6)]^(3+) and [Cr(CN)_(6)]^(3-) , the order of CFSE (Delta_(0)) in these complexes in the order:

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: Value of CFSE depends upon nature of ligand and a spectrochemical series has been made experimentally, for tetrahedral complexes, Delta is about 4/9 times to Delta_(0) (CFSE for octahedral complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. Which of the following is correct arrangement of ligand in terms of the Dq values of their complexes with any particularr 'hard' metal ion:

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: Value of CFSE depends upon nature of ligand and a spectrochemical series has been made experimentally, for tetrahedral complexes, Delta is about 4/9 times to Delta_(0) (CFSE for octahedral complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. Which of the following is correct arrangement of ligand in terms of the Dq values of their complexes with any particularr 'hard' metal ion:

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