i had one amino acid question and it was along the lines of what faulknce was talking about.
the question goes like this:
at ph 1, what will be the resonance state of a certain given amino acid. and you will see that the correct response for this answer will be protonated amino group nh3+ and protonated carboxilic groups cooh. why, because at low ph their is an excess of (h+) due to the acidity of the solution and those groups will be protonated. the reverse would be high ph/basic medium and in that case the carboxilic group would be deprotonated by the excess base and the amino group would be in its native form.
if i screwed that up anyone, please correct me if i'm wrong.
the only other aa question i could think of would be:
are all aa's chiral? and the answer would be no be glycine i believe is the lone achiral aa because its got a h r group
their may be others but i found the ochem section to be fairly straight forward - do know a bit about separation techniques though - that could have been one of the ones i missed and its easy if you study it a bit. i wasn't prepared for it
good luck
bloomer