If the CFSE of $\left[ Ti \left( H _2 O \right)_6\right]^{3+}$ is $-960 kJ / mol$, this complex will absorb maximum at wavelength ___$nm$ (nearest integer) Assume Planck's constant $( h )=64 \times 10^{-34} Js$, Speed of light $( c )=30 \times 10^8 m / s$ and Avogadro's Constant $\left( N _{ A }\right)=6 \times 10^{23} / mol$
For the complex \( [ \text{Ti}^{3+} (\text{H}_2\text{O})_6 ]^{3+} \), the electronic configuration is \( \text{Ti}^{3+}: 3d^1 \). The CFSE (Crystal Field Stabilization Energy) is given as -96.0 kJ/mol.
The formula for the CFSE is:
\[ \text{CFSE} = -0.4 \Delta_0 \]
Where \( \Delta_0 \) is the crystal field splitting energy. Using the given data:
\[ \text{CFSE} = -96 \times 10^3 \, \text{J/mol} \]
Now, solving for \( \Delta_0 \):
\[ \Delta_0 = \frac{96 \times 10^3}{6 \times 10^{23}} \quad \Rightarrow \quad \Delta_0 = 1.6 \times 10^{-19} \, \text{J} \]
Now, using the formula for the wavelength of absorption:
\[ \frac{hc}{\lambda} = \Delta_0 \]
Substitute the known values:
\[ \frac{6.4 \times 10^{-34} \times 3.0 \times 10^8}{\lambda} = 1.6 \times 10^{-19} \]
Solving for \( \lambda \):
\[ \lambda = \frac{6.4 \times 10^{-34} \times 3.0 \times 10^8}{1.6 \times 10^{-19}} = 480 \times 10^{-9} \, \text{m} \]
Thus, the wavelength is \( 480 \, \text{nm} \).


