Step 1: Understanding the Question:
We need to find the specific orbital hybridization of the central Cobalt (Co) ion in the octahedral coordination complex ion $[\text{CoF}_6]^{3-}$ using Valence Bond Theory (VBT).
Step 2: Detailed Explanation:
Let's systematically evaluate the electronic state of the central metal atom:
1.
Determine the oxidation state of Co:
Let the oxidation state of Co be $x$. Flouride ($\text{F}^-$) is a monodentate anionic ligand with a $-1$ charge.
$$ x + 6(-1) = -3 \implies x = +3 $$
Thus, Cobalt exists as a $\text{Co}^{3+}$ ion.
2.
Electronic Configuration:
Atomic number of $\text{Co} = 27$: $[\text{Ar}] 3\text{d}^7 4\text{s}^2$
For $\text{Co}^{3+}$ ion: $[\text{Ar}] 3\text{d}^6 4\text{s}^0 4\text{p}^0 4\text{d}^0$
3.
Nature of the Ligand:
Fluoride ($\text{F}^-$) is a well-known
weak field ligand. According to spectrochemical series behavior, it does not possess enough field energy to force pairing of the electrons inside the $3\text{d}$ subshell. Therefore, the six $3\text{d}$ electrons remain distributed according to Hund's rule (one paired orbital and four unpaired electrons).
4.
Orbital Hybridization:
Since the inner $3\text{d}$ orbitals are unavailable for bonding, the complex must utilize outer shell empty valence orbitals to accommodate 6 pairs of incoming ligand electrons.
The metal ion mixes one $4\text{s}$, three $4\text{p}$, and two $4\text{d}$ atomic orbitals:
$$ 4\text{s} + 4\text{p}_x + 4\text{p}_y + 4\text{p}_z + 4\text{d}_{z^2} + 4\text{d}_{x^2-y^2} \rightarrow \text{sp}^3\text{d}^2 $$
This configuration gives six empty $\text{sp}^3\text{d}^2$ outer-orbital hybrid paths to form an outer-orbital high-spin complex.
Step 3: Final Answer:
The hybridization exhibited is $\text{sp}^3\text{d}^2$, which corresponds directly to option (B).