Originally posted by TroutBum
Yes, there were a lot of synthesis problems. However, recognizing that 1, 5 carbonyls are the result of a Michael addition is the type of general principle that we needed to be familiar with. Nobody is claiming that there's no memorization. But, the idea was to do synthesis problems by recognizing the releveant reaction mechanisms at play, not by memorizing ofhundreds different reactions and then reproducing them.
We hardly did ANY problems filling in reagents and solvents. For us, it was the other way around--you end up with this product, with this added in and this added in in such and such steps. How did you get there? It required you to think through the reactions, not just memorize that adding SOCL2 gives you RCOCL, although you did need the basics memorized.
To mattorama, we're not solving the kinetics of new mechanisms here, we're talking about doing intro level Orgo.
But I agree when you say that you need to memorize the basics reactions generalized to some group reacting with another group. That's the whole trick to it. A lot of people try to memorize all the different possible reactions, without bothering to recognize the common features in any of them. For example, people might memorize "ketone plus hydroxyl yields secondary alcohol" without really knowing what's going on during the reaction--where the electrons go and why. That's what I'm talking about when I say you need to know the basics--for any reaction (brand new or not), knowing where the electrons go and why, and that involves a level of understanding beyond mere memorization, and I think it serves you better because then you can understand new reactions much better.