Thermal stability of group 2 chlorides follows the order: $\ce{BeCl2>MgCl2>CaCl2}$.
Talking about carbonates of group 2 metals, the thermal stability increases as we move down the group due to decreasing polarizing power of the cations. Why is the similar trend not observed in halides? I found an answer here which had an elaborate explanation of the fazan's rule and effect of polarizability of anions. However, that comparison was made for a single cation bonded with different halogens bonded one on one as one moves down the group. Surely, the stability in that case increases down the group as the charge density on anion decreases. The comparison made here is different. I want to know the trend when the cation is being changed and anion is same. According to Fazan's rule, the trend should be same as that for carbonates: their stability increases on moving down because charge density of cation decreases. But this is not observed in the case of chlorides. Why is that so?
When the ions electron cloud, is less polarized, the bond is less strong, leading to a less stable molecule.. Does that not suffice? – William R. Ebenezer May 16 '19 at 05:53