The correct order of the following complexes in terms of their crystal field stabilization energies $(CFSE)$ is:

  • A
    $[Co(NH_3)_4]^{2+} < [Co(NH_3)_6]^{2+} < [Co(en)_3]^{3+} < [Co(NH_3)_6]^{3+}$
  • B
    $[Co(NH_3)_4]^{2+} < [Co(NH_3)_6]^{2+} < [Co(NH_3)_6]^{3+} < [Co(en)_3]^{3+}$
  • C
    $[Co(NH_3)_6]^{2+} < [Co(NH_3)_6]^{3+} < [Co(NH_3)_4]^{2+} < [Co(en)_3]^{3+}$
  • D
    $[Co(en)_3]^{3+} < [Co(NH_3)_6]^{3+} < [Co(NH_3)_6]^{2+} < [Co(NH_3)_4]^{2+}$

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Similar Questions

The crystal field splitting energy for octahedral $\Delta _0$ and tetrahedral $\Delta _t$ complexes is related as

$\left[ Ti \left( H_{2} O \right)_{6} \right]^{3+}$ absorbs light of wavelength $498 \, nm$ during a $d-d$ transition. The octahedral splitting energy for the above complex is $....... \times 10^{-19} \, J$. (Round off to the Nearest Integer). Given: $h = 6.626 \times 10^{-34} \, Js$,$c = 3 \times 10^{8} \, ms^{-1}$.

The increasing order of field strength of ligands is:

The correct order of energy of absorption for the following metal complexes is
$A: [Ni(en)_3]^{2+}, B: [Ni(NH_3)_6]^{2+}, C: [Ni(H_2O)_6]^{2+}$

The value of $CFSE$ in a tetrahedral complex having a $3d^4$ configuration of the metal ion,surrounded by strong field ligands,will be:

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