Which one of the following statements is correct for $d^4$ ions $(P = \text{pairing energy})$?

  • A
    When $\Delta_0 > P$,low-spin complex forms
  • B
    When $\Delta_0 < P$,low-spin complex forms
  • C
    When $\Delta_0 > P$,high-spin complex forms
  • D
    When $\Delta_0 < P$,both high-spin and low-spin complexes form

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Similar Questions

For which of the following pairs of complexes is the crystal field splitting energy $\Delta_0$ for $II > \Delta_0$ for $I$?
$I$ $II$
$(a). [Cr(H_2O)_6]^{2+}$ $[Cr(H_2O)_6]^{3+}$
$(b). [Fe(H_2O)_6]^{3+}$ $[Fe(CN)_6]^{3-}$
$(c). [Fe(CN)_6]^{3-}$ $[Ru(CN)_6]^{3-}$
$(d). [NiF_6]^{4-}$ $[NiF_6]^{2-}$

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The crystal field stabilization energy of $[Co(NH_3)_6]Cl_3$ is $......... \Delta_0$

Which of the following will have maximum stabilization due to crystal field?

Calculate the Crystal Field Stabilization Energy $(CFSE)$ for a high-spin $d^4$ tetrahedral complex.

The electronic spectrum of $[Ti(H_2O)_6]^{3+}$ shows a single broad peak with a maximum at $20,300 \, cm^{-1}$. The crystal field stabilization energy $(CFSE)$ of the complex ion,in $kJ \, mol^{-1}$,is :

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