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

  • A
    $a, b, c$
  • B
    $b, c, d$
  • C
    $a, b, c, d$
  • D
    $c, d$

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Similar Questions

The correct statements among $I$ to $III$ are:
$I$. Valence bond theory cannot explain the color exhibited by transition metal complexes.
$II$. Valence bond theory can predict quantitatively the magnetic properties of transition metal complexes.
$III$. Valence bond theory cannot distinguish ligands as weak and strong field ones.

Arrange the following complex ions in increasing order of crystal field splitting energy $(\Delta_{0}):$ $[Cr(Cl)_{6}]^{3-}, [Cr(CN)_{6}]^{3-}, [Cr(NH_{3})_{6}]^{3+}$

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Write a note on crystal field theory.

Identify the complex ion with electronic configuration $t_{2g}^3 e_g^2$.

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

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