To determine the hybridization, we calculate the steric number (SN) for the central atom in each species. The steric number is the sum of the number of atoms bonded to the central atom and the number of lone pairs on the central atom. It can be calculated using the formula: SN = (Valence electrons of central atom + electrons from ligands - charge) / 2.
The hybridization corresponds to the steric number as follows:
| Species | Central Atom | Valence e- | Bonds with F | Charge | SN Calculation (VE + Ligands - Charge) / 2 | Steric Number (SN) | Lone Pairs (SN - Bonds) | Hybridization |
| $XeF_6$ | Xe | 8 | 6 | 0 | (8 + 6 - 0) / 2 | 7 | 1 | $sp^3d^3$ |
| $BrF_6^+$ | Br | 7 | 6 | +1 | (7 + 6 - 1) / 2 | 6 | 0 | $sp^3d^2$ |
| $IF_5$ | I | 7 | 5 | 0 | (7 + 5 - 0) / 2 | 6 | 1 | $sp^3d^2$ |
| $XeF_4$ | Xe | 8 | 4 | 0 | (8 + 4 - 0) / 2 | 6 | 2 | $sp^3d^2$ |
Based on the calculations:
Therefore, $XeF_6$ is the species where $sp^3d^2$ hybridization is not associated.
The calculated magnetic moment for low spin $[Ru(EDTA)]^-$ is
Nickel combines with a uninegative monodentate ligand (X−) to form a paramagnetic complex [NiX4]2−. The hybridisation involved and number of unpaired electrons present in the complex are respectively
Which of the following statements is incorrect ?
The crystal field splitting energy of $[\text{Co(oxalate)}_3]^{3-}$ complex is '$n$' times that of the $[\text{Cr(oxalate)}_3]^{3-}$ complex. Here '$n$' is ___________. (Assume $\Delta_o >> P$)