$[Fe(CN)_{6}]^{3-}$ is an inner orbital complex. Ignoring the pairing energy,the value of crystal field stabilization energy for this complex is $(-)\;\dots \;\Delta_{o}$.

  • A
    $5$
  • B
    $4$
  • C
    $3$
  • D
    $2$

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Similar Questions

According to crystal field theory, for which of the following coordination entities is $\Delta_o$ maximum?

Match the $LIST$-$I$ with $LIST$-$II$:
List-$I$ (Electronic configuration of tetrahedral metal ion) List-$II$ (Crystal Field Stabilization Energy $(\Delta_t)$)
$A$. $d^2$ $I$. $-0.6$
$B$. $d^4$ $II$. $-0.8$
$C$. $d^6$ $III$. $-1.2$
$D$. $d^8$ $IV$. $-0.4$

Arrange the following Cobalt complexes in the order of increasing Crystal Field Stabilization Energy $(CFSE)$ value.
Complexes: $[CoF_{6}]^{3-}, [Co(H_{2}O)_{6}]^{2+}, [Co(NH_{3})_{6}]^{3+}$ and $[Co(en)_{3}]^{3+}$
$A: [CoF_{6}]^{3-}, B: [Co(H_{2}O)_{6}]^{2+}, C: [Co(NH_{3})_{6}]^{3+}, D: [Co(en)_{3}]^{3+}$
Choose the correct option:

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$

$[Fe(CN)_6]^{4-}$ and $[Fe(H_2O)_6]^{2+}$ show different colours in dilute solution because

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