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AlCl3 promotes the chlorination of aromatic molecules such as benzene, when chlorine (Cl2) is added. The AlCl3 is regenerated, and HCl is a byproduct. The Friedel-Crafts reaction is also promoted by AlCl3. In Friedel-Crafts acylation, the product is an aromatic ketone, and the byproduct is HCl.
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Not much I suggest. 0-xylene is not significantly soluble in water. In any case rather than acting as acid catalyst, aluminium chloride in water is a rather boring salt which gives cations and anions in solution.
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