Thanks for replying. Could you elaborate on the respect in which you consider the equation for change in Gibbs free energy is misleading? I appreciate it relates to changes occurring at constant pressure (H = U + PV), which is why chemists use it so much, as it is appropriate for the conditions of a great many chemical reactions in the lab. Enthalpy change is thus the sum of change in chemical energy plus any incidental "PV" work done on, or by, the atmosphere during the change. But how is it misleading, exactly?
$$U$$ represents the system's total intrinsic energy, not chemical energy. Changes in $$H$$ represent changes in $$U$$ after subtracting the work done in changing volume, which usually leaves heat + chemical/electrical work. My objection to your formula is that it obscures the fact that $$H$$ and $$S$$ are themselves functions of temperature and pressure, so you can't simply use this formula with the values quoted in tables at SATP in order to say whether a reaction occurs or not. You can however either refer to experimental values determined for the required pressure and temperature, or else use the system's thermodynamic equation of state to theoretically calculate these values based on known values at some other pressure and temp.
Secondly, I do not follow why you mention electrical work. If we talk about the energy state of a crystalline solid and compare it to either the corresponding liquid (as I did) or to a dissolved solution (as it seems you are doing), where does electrical work come into it?
Well let's not get confused over the crystals we're speaking of. Captain Kremmen was talking about the crystals that form out of solution at increased entropy. As for electrical work, any chemical reaction involves the exchange of electric charge, and so in theory the remaining energy left over from a reversible reaction (after volume work done on/by the atmosphere and heat exchanged) can be harnessed as electrical work, or electrical work can be performed to force the reaction.