Quote:
Originally Posted by ha ha
if i only have, for example, 91% sulfuric acid, or... 69% sulfuric acid, will the synthesis simply not work?
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Well, that depends...
Ignoring ionic disassociation for a sec, let's presume your titrating a base to a nice, balanced salt. Not a "synth," but good enough for this discussion for a sec.
If things are calling for 10ml of 91% sulfuric acid, and you throw in 69ml of 69% sulfuric acid... you will have much, much less H2SO4. This means... much less of the salt is formed, much greater unreacted byproducts are befouling your cleanup, etc...
Now, let's make this even moar bitchin'. Let's say you've got 2 mols of monobromobenzene, 'n 1 mol of paraquinone. Fun, huh? 'n let's say, you've found a solvent which magnesium will actually dissolve in. Probably a wierd-ass freaking solvent, maybe mercury, but we'll presume it works and is inert.
Now... let's say that instead of the volume of 3 mols of solvent at the temperature and pressure of measurement, at 66% concentration, you throw in 3 mols at... 11% concentration...
Normally, you'd think "oh... no problem... just... 1/3rd the yield and a bunch of crap that I hope I'll have to clean up." But... no, no that is not the case.
For starters, any oxygen present is running around contaminating your magnesium while the bromobenzene is floating around this sparse, sparse sea trying to look for what's barely there. There's a risk that you'll get
zip for yield, if there's enough oxygen.
Worse still, in the reaction given... the reagent you left unreacted is going to run the risk of brutally attacking the theoretical final product, a triphenyldiol with a partially dearomatized central ring. 'n it's your fault for leaving it in there. So, even if you pull off some yields in spite of degredation at such a low-ass concentration and diluted reaction rate, you could still lose it all.
So, factoring in what we dropped in the first paragraph...
- dilution might retard the reaction while accelerating degradation.
- dilution might prevent concentration required for proper ionization in pH dependent reactions.
...and, the main thing I wrote too many paragraphs about...
- dilution may fuck up your weights and quantities if you don't fucking account for it.
That last one is the big important one, and the rest can be obscenely important, or completely unimportant, depending on the reaction. Know your reaction, and exactlywhat is going on.
...but other times, as long as you standardize to the same molar ratios, it doesn't really fucking matter. All varies from reaction to reaction. Have fun.