Carbon donor ligands are strong ligands and usually form low spin complexes. Among the complexes given below,select the high spin complex.

  • A
    $[Fe(CN)_6]^{3-}$
  • B
    $[Fe(CN)_6]^{4-}$
  • C
    $[Fe(C_2O_4)_3]^{3-}$
  • D
    none of these

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Similar Questions

$[Fe(CN)_{6}]^{4-}$ and $[Fe(H_{2}O)_{6}]^{2+}$ are of different colours in dilute solutions. Why?

The values of the crystal field stabilization energies for a high spin $d^{6}$ metal ion in octahedral and tetrahedral fields,respectively,are :

The wavelengths of light absorbed by the complexes $[Ni(H_2O)_6]^{2+}$,$[Ni(en)_3]^{2+}$,and $[Ni(H_2O)_4en]^{2+}$ are $\lambda_1$,$\lambda_2$,and $\lambda_3$ respectively. The correct order of wavelengths is:

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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The number of unpaired $d$-electrons in $[Co(H_2O)_6]^{3+}$ is $\qquad$

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