Match the following complexes in List-$I$ with their electronic configurations in List-$II$.
List-$I$ (Complex)List-$II$ (Electronic configuration of metal/ion)
$A. [Co(NH_3)_6]^{3+}$$I. t_{2g}^5 e_g^0$
$B. [CoF_6]^{3-}$$II. t_{2g}^6 e_g^0$
$C. [Ni(CO)_4]$$III. t_{2g}^4 e_g^2$
$D. [Fe(CN)_6]^{3-}$$IV. t^4 e^6$

  • A
    $A-II, B-III, C-IV, D-I$
  • B
    $A-III, B-IV, C-II, D-I$
  • C
    $A-IV, B-III, C-I, D-II$
  • D
    $A-II, B-I, C-IV, D-III$

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Similar Questions

Arrange the following in increasing order of their crystal field splitting energy:
$I. [Co(H_2O)_6]^{3+}$
$II. [Co(NH_3)_6]^{3+}$
$III. [Co(CN)_6]^{3-}$
$IV. [CoF_6]^{3-}$

Which among the following complexes is associated with the maximum wavelength of light absorbed?

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Identify the weak field ligand from the following.

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.

The crystal field stabilisation energy $(CFSE)$ and the spin-only magnetic moment in Bohr Magneton $(BM)$ for the complex $K_3[Fe(CN)_6]$ are,respectively

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