Step 1: Find number of unpaired electrons from \(\mu_{\text{so}}\).
Spin-only formula: \(\mu_{\text{so}}=\sqrt{n(n+2)}\,\mathrm{BM}\). Given \(5.9\,\mathrm{BM}\) \(\Rightarrow\) \(n(n+2)\approx(5.9)^2\approx34.8\). The nearest integer solution is \(n=5\) (since \(\sqrt{5(5+2)}=\sqrt{35}=5.92\,\mathrm{BM}\)).
Step 2: Determine metal oxidation state and \(d\)-count.
Let oxidation state of Mn be \(x\): \(x+4(-1)=-2 $\Rightarrow$ x=+2\). Thus \(\mathrm{Mn^{2+}}\) is \(d^5\).
Step 3: Decide geometry.
\(\mathrm{Br^-}\) is a weak-field ligand, so pairing is unfavorable; a \(d^5\) ion remains high spin with 5 unpaired electrons—consistent with the observed \(\mu\). Four-coordinate \(\mathrm{Mn^{2+}}\) with weak-field ligands prefers tetrahedral over square planar (which is typical for \(d^8\) ions and would require strong-field stabilization).
\[
\boxed{\text{Geometry of }[\mathrm{MnBr}_4]^{2-}\ \text{is tetrahedral.}}
\]
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.