The \(\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{6}^{3+}\) ion is diamagnetic, but \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{2+}\) is paramagnetic. Explain.

Short Answer

Expert verified
The \(\mathrm{Co}(\mathrm{NH}_{3})_{6}^{3+}\) ion is diamagnetic because there are no unpaired electrons in its d-orbitals, as all electrons are paired up in the t₂g orbitals. On the other hand, \(\mathrm{Fe}(H_{2}O)_{6}^{2+}\) is paramagnetic due to the presence of four unpaired electrons in its d-orbitals, caused by the smaller splitting in the weaker ligand field of H₂O.

Step by step solution

01

Writing Electronic Configurations

First, write down the electronic configurations of the central metal ions, Cobalt (Co) and Iron (Fe), considering their respective oxidation states. For Co in \(\mathrm{Co}(\mathrm{NH}_3)_6^{3+}\), the oxidation state of Co is +3. For Fe in \(\mathrm{Fe}(H_2O)_6^{2+}\), the oxidation state of Fe is +2. The electronic configuration of Co and Fe in their neutral states are: Co: [Ar] 4s² 3d⁷ Fe: [Ar] 4s² 3d⁶ Now let's remove the appropriate number of electrons to obtain the electronic configurations of Co³⁺ and Fe²⁺: Co³⁺: [Ar] 3d⁶ Fe²⁺: [Ar] 3d⁴
02

Analysing the Ligand Field in Octahedral Complexes

Now we need to understand the ligand field splitting in the octahedral complexes. The ligands surrounding the metal ions in both complexes cause the d-orbitals to split into two sets of different energies: three orbitals of lower energy (t₂g) and two orbitals of higher energy (e_g). The strong field ligand, NH₃, in Co complex results in a larger splitting, represented by Δ₀ (crystal field splitting energy), causing electrons to first fill the lower energy t₂g orbitals. On the other hand, H₂O is a weaker field ligand in Fe complex leading to smaller splitting, represented by Δ₀, such that electrons might not necessarily fill the lower t₂g orbitals first.
03

Filling the Electrons in the Split Orbitals

Now, fill up the d-electrons with respect to the splitting of the ligand field and Hund's rule (keep electrons unpaired in degenerate orbitals until all orbitals are half-filled): Co³⁺: In the octahedral complex, the t₂g orbitals are completely filled and the e_g orbitals are empty: t₂g↑↓ t₂g↑↓ t₂g↑↓ e_g↑-- e_g↑-- Fe²⁺: In the octahedral complex, the t₂g orbitals are half-filled and one of the e_g orbitals has an unpaired electron: t₂g↑↓ t₂g↑-- t₂g↑-- e_g↑-- e_g↑--
04

Analyzing Magnetic Properties

Now, we can determine the magnetic properties of both complexes: In \(\mathrm{Co}(\mathrm{NH}_3)_6^{3+}\) complex, all the electrons are paired up with no unpaired electrons in its d-orbitals: t₂g↑↓ t₂g↑↓ t₂g↑↓ e_g↑-- e_g↑--. This complex is diamagnetic, having no unpaired electrons. In \(\mathrm{Fe}(H_2O)_6^{2+}\) complex, there are four unpaired electrons in the d-orbitals: t₂g↑↓ t₂g↑-- t₂g↑-- e_g↑-- e_g↑--. This complex is paramagnetic due to the presence of unpaired electrons. In summary, the \(\mathrm{Co}(\mathrm{NH}_{3})_{6}^{3+}\) ion is diamagnetic because there are no unpaired electrons in its d-orbitals, while \(\mathrm{Fe}(H_{2}O)_{6}^{2+}\) is paramagnetic due to the presence of four unpaired electrons in its d-orbitals.

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