The correct order for wavelengths of absorption in the visible region for the following complexes will be

  • A
    $[Ni(NH_3)_6]^{2+} < [Ni(H_2O)_6]^{2+} < [Ni(NO_2)_6]^{4-}$
  • B
    $[Ni(NO_2)_6]^{4-} < [Ni(NH_3)_6]^{2+} < [Ni(H_2O)_6]^{2+}$
  • C
    $[Ni(NH_3)_6]^{2+} < [Ni(NO_2)_6]^{4-} < [Ni(H_2O)_6]^{2+}$
  • D
    $[Ni(NO_2)_6]^{4-} < [Ni(H_2O)_6]^{2+} < [Ni(NH_3)_6]^{2+}$

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Similar Questions

Match List-$I$ with List-$II$:
List-$I$ (Complex) List-$II$ ($CFSE$ in $\Delta_0$)
$A$. $[Ti(H_2O)_6]^{2+}$ $I$. $-1.2$
$B$. $[V(H_2O)_6]^{2+}$ $II$. $-0.8$
$C$. $[Mn(H_2O)_6]^{3+}$ $III$. $-0.6$
$D$. $[Fe(H_2O)_6]^{3+}$ $IV$. $0$

The electronic configuration of a metal ion in its complex is $[Ar] 3d^4$. For this metal complex,$\Delta_o < P$ ($P=$ energy required for electron pairing in a single orbital). The distribution of electrons in the complex is:

The metal $d-$orbitals that directly face the ligands in $K_3[Co(CN)_6]$ are:

The transition metal complex with the highest value of crystal field splitting $(\Delta_{0})$ is ........ .

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

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