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What is the nature of the bonding in anhydrous $\mathrm{AlCl}_3$ and hydrated $\mathrm{AlCl}_3$ respectively?
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Covalent and ionic
Many simple compounds of elements such as $\mathrm{AlCl}_3, \mathrm{GaCl}_3$ and $\mathrm{InCl}_3$ are covalent while anhydrous but in aqueous solution, these are ionic in nature. In anhydrous condition, the (charge/radius) ratio, i.e. polarisability of $\mathrm{Al}^{3+}$ is high and hence, according to Fajans' rule, $\mathrm{Al}^{3+}$ polarises $\mathrm{Cl}^{-}$ions to large extent, there introducing covalent character in the compound, i.e. $\mathrm{AlCl}_3$ behaves as a covalent compound in anhydrous conditions.
In aqueous medium the ions get hydrated, because the amount of hydration enthalpy released exceeds, the sum total of ionisation enthalpy required.
Since, the (charge/radius ratio of hydrated aluminium ion is much smaller as compared to that of $\mathrm{Al}^{3+}$, the tendency of $\left[\mathrm{Al}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{3+}$ to polarise hydrated $\mathrm{Cl}^{\ominus}$ ion decreases and the resulting hydrated compound is ionic in nature.
In aqueous medium the ions get hydrated, because the amount of hydration enthalpy released exceeds, the sum total of ionisation enthalpy required.
Since, the (charge/radius ratio of hydrated aluminium ion is much smaller as compared to that of $\mathrm{Al}^{3+}$, the tendency of $\left[\mathrm{Al}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{3+}$ to polarise hydrated $\mathrm{Cl}^{\ominus}$ ion decreases and the resulting hydrated compound is ionic in nature.
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