Home
Class 12
CHEMISTRY
Crystal field stabilization energy for h...

Crystal field stabilization energy for high spin `d^4` octahedral complex is

A

`-1.8Delta_(0)`

B

`-1.6Delta_(0)+P`

C

`-1.2Delta_(0)`

D

`-0.6Delta_(0)`

Text Solution

Verified by Experts

The correct Answer is:
D

(d) Key Idea In case of high spin complex, `Delta_(o)` is small. Than the pairing energy. That means, the energy required to pair up the fourth electorn with the electrons of lower energy d-orbitals would be higher than that required to place the electrons in the higher d-orbital Thus, painng does not occur. For high spin `d^(4)` octahedral complex.

`therefore` Crystal field stabilisation energy
`=(-3xx0.4+1xx0.6)Delta_(o)`
`=(-1.2+0.6)Delta_(o)=-0.6Delta_(o)`
Promotional Banner

Similar Questions

Explore conceptually related problems

The values of the crystal field stabilization energies for a high spin d^6 metal ion in octahedral and tetrahedral fields, respectively, are :

Crystal field stabilization energy of high spin complex cation having d_5 configuration in an octahedral field is

The magnitude of crystal field stabilisation energy (CFSE of Delta_(1) ) in tetrahedral complexes is considerably less than that in the octahderal field. Because

The magnitude of crystal field stabilisation energy (CFSE of Delta_(1) ) in tetrahedral complexes is considerably less than that in the octahderal field. Because

Statement-1: [Co^(II)(NH)_(3))_(6)]^(2+) is not readily oxidized to [Co^(III)(NH_(3))_(6)]^(3+) when air is bubbled through it. Statement-2: Crystal field stabilization energy of Co(+III) with a d^(6) configuration is higher then for Co(+III) with a d^(7) arrangement.

The complex ion that will lose its crystal field stabilization energy upon oxidation of its metal to +3 state is :

In which structure crystal field splitting energey (CFSE) for octahedral complex will be zero when DeltaltP .

The value of CFSE (Crystal field stabilisation energy) for Na_4[FeF_6] complex is (ignore pairing energy)

The enthalpy of hydration of the Fe^(2+) ion is 11.4kcal//mol higher than would be expected if there were no crystal field stabillisation energey Assuming the equo complex to be high spin estimate the magnitude of Delta_(0) for [Fe(H_(2)O)_(6)]^(2+) ion .

Using CFT depict the electronic configuration of the rhodium ion (Rh^(2+)) in an octahedral field for which the crystal field splitting Delta_(0) is greater than the pairing eneryg P (b) Calculate the crystal field stabilisation energy for this configuration (in terms of Delta andP) .