Oxidation State for Chromium in the complex
is (+2) and valance shell electronic configuration is
.
Now d-orbital can have two electronic configuration, such as
high spin
or low spin
depending upon the splitting power of ligands. If the ligand is
weak field ligand, the complex will be high spin complex. If the
ligand is strong field ligand, the complex will be low spin
complex.
Here comes a factor Pairing energy which is the
energy penalty for putting two electrons in the same orbital,
resulting from the electrostatic repulsion between electrons.
For configuration
first three electrons will go to the
orbitals. If
the crystal field splitting energy
is lower than the pairing energy then the fourth electron will go
to the
orbital, hence
generate a high spin complex. If the crystal field splitting energy
is higher than the pairing energy then the fourth electron will go
to the
orbital, hence
we will end up with low spin complex.

In this complex
,
is acting as a
strong field ligand as it is given in the question that the crystal
field splitting energy
is higher than the pairing energy
,
hence the complex is a low spin complex.

Crystal Field Stabilization Energy (CFSE) =
* number of t2g electrons +
* number of eg electrons + P * number of pair of paired
electrons =
* 4 +
* 0 + P * 1 =
=
P
* number of pair of paired electrons = P * 0 = 0 kJ
mol-1
CFSE =
=
[ANSWER]
Calculate the crystal field stabilization energy valiue for the complex Cr(NH)J*. The crystal field splitting energy...
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The wavelength of light (in nanometers) that is absorbed by a complex that has a crystal-field splitting energy of 3.30×102 kJ/mol is _____. (h = 6.626 × 10−34 J·s, c = 3.00 × 108 m/s)