Step 1: Recall the property of coordination compounds.
Coordination compounds are mainly formed by transition metal ions because they have vacant d-orbitals available for coordination with ligands.
Step 2: Analyze each ion.
- (A) Na$^{+}$: Belongs to group 1 (s-block). It has no vacant d-orbitals and does not form coordination compounds.
- (B) Cr$^{2+}$: Transition metal ion, forms complexes (e.g., [Cr(H$_2$O)$_6$]$^{2+}$).
- (C) Co$^{2+}$: Transition metal ion, forms complexes (e.g., [Co(NH$_3$)$_6$]$^{2+}$).
- (D) Cr$^{3+}$: Transition metal ion, forms complexes (e.g., [Cr(H$_2$O)$_6$]$^{3+}$).
Step 3: Conclusion.
Only Na$^{+}$ does not form coordination compounds because it lacks d-orbitals.
\[
\boxed{\text{Na}^{+}}
\]
The correct IUPAC name of \([ \text{Pt}(\text{NH}_3)_2\text{Cl}_2 ]^{2+} \) is:
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
What is crystal field splitting energy?
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
On the basis of CFT, explain why [Ti(H$_2$O)$_6$]Cl$_3$ complex is coloured? What happens on heating the complex [Ti(H$_2$O)$_6$]Cl$_3$? Give reason.