To solve the problem, we need to calculate the spin-only magnetic moment of the Cr$^{3+}$ ion. The formula for the spin-only magnetic moment is given by:
1. Determining the Electron Configuration of Cr$^{3+}$:
The atomic number of Cr is 24, so the ground-state electron configuration of Cr is [Ar] 3d5 4s1. For Cr$^{3+}$, we remove three electrons. The configuration becomes [Ar] 3d3, meaning Cr$^{3+}$ has 3 unpaired electrons in its 3d orbital.
2. Formula for Spin-Only Magnetic Moment:
The spin-only magnetic moment is given by:
$ \mu_{\text{spin}} = \sqrt{n(n+2)} $
where $n$ is the number of unpaired electrons. In this case, $n = 3$.
3. Substituting the Value of $n$:
Substituting $n = 3$ into the formula:
$ \mu_{\text{spin}} = \sqrt{3(3+2)} = \sqrt{3 \times 5} = \sqrt{15} \approx 3.87 \, \mu_{\text{B}} $
Final Answer:
The spin-only magnetic moment of Cr$^{3+}$ ion is approximately $3.87 \, \mu_{\text{B}}$.
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.