This question requires analyzing the provided coordination complexes to determine the electron count in the \( t_{2g} \) orbitals of the most stable complex ion.
The given complexes are analyzed as follows:
- \([Fe(NH_3)_6]^{3+}\):
- Ligand: Ammonia (\( NH_3 \)) is a strong field ligand.
- Iron oxidation state: \( +3 \).
- \( Fe^{3+} \) electronic configuration: \( [Ar] \, 3d^5 \).
- Strong field ligands induce d-orbital splitting (\( t_{2g} \) and \( e_g \)) and electron pairing.
- The \( t_{2g} \) orbitals are filled before \( e_g \). In this case, 4 electrons occupy the \( t_{2g} \) orbitals.
- \([Fe(Cl)_6]^{3-}\):
- Ligand: Chloride (\( Cl^- \)) is a weak field ligand.
- Iron oxidation state: \( +3 \).
- \( Fe^{3+} \) electronic configuration: \( [Ar] \, 3d^5 \).
- Weak field ligands do not cause electron pairing.
- \([Fe(C_2O_4)_3]^{3-}\):
- Ligand: Oxalate (\( C_2O_4^{2-} \)) is a strong field ligand.
- Iron oxidation state: \( +3 \).
- \( Fe^{3+} \) electronic configuration: \( [Ar] \, 3d^5 \).
- Electron pairing occurs with strong field ligands.
- \([Fe(H_2O)_6]^{3+}\):
- Ligand: Water (\( H_2O \)) is a weak field ligand.
- Iron oxidation state: \( +3 \).
- \( Fe^{3+} \) electronic configuration: \( [Ar] \, 3d^5 \).
- No electron pairing occurs.
Based on the analysis, \( [Fe(C_2O_4)_3]^{3-} \) is the most stable complex due to the maximum electron occupation in the \( t_{2g} \) orbitals, resulting in a \( t_{2g}^5 \) configuration.
The second part of the question concerns the nature of the vanadium oxide \( V_2O_x \).
Vanadium exhibits multiple oxidation states, leading to various oxides:
- For \( x=5 \) in \( V_2O_5 \), the oxide is amphoteric, exhibiting both acidic and basic properties.
The nature of this oxide is Amphoteric.