I don't know, it wanst solid, have you ever shaken up those little computer mice or somethig like that with a blue oil and a toy boad and water inside, the blue "ocean" breaks up into tiny bubbles, tolounene's and ethanol/methanol's (it was a mix of both) viscosity are low so it makes sense that there are tiny little bubbles of toloene in the MeOH and EtOH solution, they are just so small they appear as a white cloudiness that distorts light around the edges of the spherical bubles, perhaps my HCl was so electrophilic it attacked the benzene ring and formed a carbocation, relesed an extra H+ and this might have formed some weird shit, I just don't know were that proton would go, primary alcohols like MeOH and EtOH need high temperatures to decompose into water or an alkene with an acid catalyst, could I have some form of oxonium ion?
Perhaps if this happened the p,o[/I-]chloro-tolouene delocalized like a salt in the alcohols? I just dont realy see how that could happen though as the chlorine would take an an extra electron with it and fuck up the aromatic structure, highly unfavorable