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

  • A
    $I > II > IV > III$
  • B
    $III > II > IV > I$
  • C
    $III > I > IV > II$
  • D
    $III > IV > I > II$

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Similar Questions

Complete removal of both the axial ligands (along the $z-$ axis) from an octahedral complex leads to which of the following splitting patterns? (relative orbital energies not on scale)

Match the electronic configurations in List-$I$ with appropriate metal complex ions in List-$II$ and choose the correct option.
[Atomic Number: $Fe=26, Mn=25, Co=27$]
List-$I$ List-$II$
$P$. $t_{2g}^6 e_g^0$ $1$. $[Fe(H_2O)_6]^{2+}$
$Q$. $t_{2g}^3 e_g^2$ $2$. $[Mn(H_2O)_6]^{2+}$
$R$. $e^2 t_2^3$ $3$. $[Co(NH_3)_6]^{3+}$
$S$. $t_{2g}^4 e_g^2$ $4$. $[FeCl_4]^{-}$
$5$. $[CoCl_4]^{2-}$

Why are low spin tetrahedral complexes not formed?

Crystal field splitting energy $(CFSE)$ for $[CoCl_6]^{4-}$ is $18000 \ cm^{-1}$. The crystal field splitting energy $(CFSE)$ for $[CoCl_4]^{2-}$ will be (in $cm^{-1}$)

Which of the following ligands will cause the smallest crystal field splitting?

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