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 :

  • A
    $242.5$
  • B
    $83.7$
  • C
    $145.5$
  • D
    $97$

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Similar Questions

The crystal field theory is successful in explaining which of the following?
$I.$ Ligands as point charges;
$II.$ Formation and structures of complexes.
$III.$ Colour;
$IV.$ Magnetic properties;
$V.$ Covalent character of metal-ligand bonding.

The total number of unpaired electrons present in the $d^3$, $d^4$ (low spin), $d^5$ (high spin), $d^6$ (high spin), and $d^7$ (low spin) octahedral complex systems is . . . . . . .

The correct order of decreasing field strength of the below given ligands is
$I$. $NCS^{-}$$II$. $S^{2-}$
$III$. $en$$IV$. $SCN^{-}$

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

The electronic spectrum of $[Ti(H_2O)_6]^{3+}$ gives a single broad peak with a maxima at $20300 \, cm^{-1}$. The crystal field stabilization energy is equal to .......... $kJ \, mol^{-1}$

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