I asked that because as far as I know and our textbook suggests, the concentration of liquids and solids is always the same during a reaction and I'm facing some kind of irony here!
this is kind of generalized...
in
most reactions you might ignore the change of (excess of) solvent , and the change in (enough) undissolved solids ref. resulting active surface thereof,
if you were into LMA calculations (!)
with the example at hand , you've reached the limit of above approximations
So unfortunately, I haven't even seen this reaction or any other reaction with my eyes. I have no idea how these reactions occur or how, for example, MgCO3 turns into MgO...
It's pretty much the same setup you use when you wish to turn CaCO
3 into CaO :
"calcination"talking reality:
- in a technical setup, the speed of the process is next to perfect 0.th order, as it completely depends on energy input
- if it wasn't for energy input running the show, the process would be of "negative" (!) order in the beginning , i.e. increase speed once it started ( I know, this sounds absurd, but that's how it is: at ~ 800°C with the carbon dioxide forming, the material becomes porous, even might bloat, and will increase it's effective, reactive surface drastically, overcompensating the effect of MgO forming and MgCO
3 loss)
- after that (still without energy input ruling the game) the other effects will beginn to kick in, and you would switch to first order kinetics incrementally.
- by the end of the day, MgCO
3 "incorporated" in MgO would have a hard time to outgas , which would provoke still another type of kinetics, ruled by the effective outgassing properties of the aggregates forming
so much for reality
Anyway, don't be too harsh with your books here: it's very hard to find a good (pseudo) first order kinetics in school, for teaching purposes.
maybe the reaction of Mg ribbons in aq. HCl , in the beginning of the reaction
regards
Ingo