Select the option with correct property -
Match List I with List II
| List - I (Complex ion) |
List - II (Electronic Configuration) |
||
|---|---|---|---|
| (A) | $$\mathrm{[Cr(H_2O)_6]^{3+}}$$ | (I) | $$t_{2 g}{ }^2 e_g^0$$ |
| (B) | $$\left[\mathrm{Fe}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{3+}$$ | (II) | $$t_{2 g}{ }^3 e_g{ }^0$$ |
| (C) | $$\left[\mathrm{Ni}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+}$$ | (III) | $$t_{2 g}{ }^3 e_g{ }^2$$ |
| (D) | $$\left[\mathrm{V}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{3+}$$ | (IV) | $$t_{2 g}{ }^6 e_g^2$$ |
Choose the correct answer from the options given below:
The correct statements from following are:
A. The strength of anionic ligands can be explained by crystal field theory.
B. Valence bond theory does not give a quantitative interpretation of kinetic stability of coordination compounds.
C. The hybridization involved in formation of $$\left[\mathrm{Ni}(\mathrm{CN})_4\right]^{2-}$$ complex is $$\mathrm{dsp}^2$$.
D. The number of possible isomer(s) of cis- $$\left[\mathrm{PtCl}_2(\mathrm{en})_2\right]^{2+}$$ is one
Choose the correct answer from the options given below:
The coordination geometry around the manganese in decacarbonyldimanganese $$(0)$$ is
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