The crystal field stabilization energy (CFSE) depends on the oxidation state and the ligand field strength.
Generally:
- The higher the oxidation state of the metal, the stronger the ligand field and the higher the CFSE.
- \( \text{NH}_3 \) is a stronger field ligand than \( \text{en} \) (ethylenediamine).
Thus: - \( [\text{Co(NH}_3)_4]^{2+} \) will have the lowest CFSE, as it is in a lower oxidation state.
- \( [\text{Co(NH}_3)_6]^{2+} \) has a higher CFSE compared to \( [\text{Co(NH}_3)_4]^{2+} \).
- \( [\text{Co(NH}_3)_6]^{3+} \) has a higher oxidation state, leading to higher CFSE.
- \( [\text{Co(en)}_3]^{3+} \) has the highest CFSE due to the strong ligand field of \( \text{en} \).
Hence, the correct order is:
\[[\text{Co(NH}_3)_4]^{2+} < [\text{Co(NH}_3)_6]^{2+}<[\text{Co(NH}_3)_6]^{3+} < [\text{Co(en)}_3]^{3+}\]Based on Crystal Field theory, match the Complex ions listed in Column I with the electronic configuration in the d orbitals of the central metal ion listed in Column II.
Let A be a 3 × 3 matrix such that \(\text{det}(A) = 5\). If \(\text{det}(3 \, \text{adj}(2A)) = 2^{\alpha \cdot 3^{\beta} \cdot 5^{\gamma}}\), then \( (\alpha + \beta + \gamma) \) is equal to:
Let \( \alpha, \beta \) be the roots of the equation \( x^2 - ax - b = 0 \) with \( \text{Im}(\alpha) < \text{Im}(\beta) \). Let \( P_n = \alpha^n - \beta^n \). If \[ P_3 = -5\sqrt{7}, \quad P_4 = -3\sqrt{7}, \quad P_5 = 11\sqrt{7}, \quad P_6 = 45\sqrt{7}, \] then \( |\alpha^4 + \beta^4| \) is equal to: