To determine the decreasing order of unpaired electrons in the low spin octahedral complexes of the transition metal ions \( \text{Mn}^{3+}, \text{Cr}^{3+}, \text{Fe}^{3+}, \) and \( \text{Co}^{3+} \), we need to consider their electronic configurations and the effect of crystal field splitting in a low spin configuration.
In a low spin octahedral complex, the strong field ligands cause a significant splitting of the \(d\)-orbitals, leading to a preference for electrons to pair up in the lower energy \(t_{2g}\) orbitals before occupying the higher energy \(e_g\) orbitals. Let's examine each ion:
Based on the calculated number of unpaired electrons:
| Ion | Unpaired Electrons |
|---|---|
| \( \text{Cr}^{3+} \) | 3 |
| \( \text{Mn}^{3+} \) | 2 |
| \( \text{Fe}^{3+} \) | 1 |
| \( \text{Co}^{3+} \) | 0 |
Thus, the correct decreasing order of unpaired electrons in their respective \( d \)-orbitals of the complexes is \(\text{Cr}^{3+} > \text{Mn}^{3+} > \text{Fe}^{3+} > \text{Co}^{3+}\). This matches the given correct answer.

For an ideal gas, a cyclic process ABCA as shown in the P–T diagram. When represented in P–V plot, it would be 