What is thermodynamic control? (Directing a reaction towards the most stable product. - GS).

Why does having a destabilized nucleophile in an SN2 reaction decrease the free energy of activation? (Because the transition state retains its energy, so the activation barrier is lower. - GS).

How does a polar, protic solvent reduce the free energy of activation and stabilize an intermediate in an SN1 reaction? (By solvation of the very polar transition state - GS). And, why does a stabilized intermediate reduce the energy barrier? (Because the less polar starting compound is not stabilized as efficiently as the transition state - GS).

Can you just briefly explain what a meso compound is? Is it just a compound that hasn't been distinguished between cis and trans?(No. It is an achiral compound with chiral centers. - GS).

Dr. Sereda, I was looking over some of the previous year’s quizzes and in the preparation of 5-methyl-2-hexyne from propyne, what would be the nucleophile? Would it be the same as the alkylating agent? Thanks. (The nucleophile is deprotonated alkyne, which attacks the alkylating agent and kicks out the leaving group from it. Overall, it results in the introduction of the alkyl group to the alkyne. - GS).

How do you know, when looking at a Newman projection, if it is staggered or eclipsed? (Eclipsed conformations have three dihedrals of 0o, staggered conformations have none. - GS).

How do you prove that the Beckmann’s rearrangement pathway where the leaving group and alkyl migration occur simultaneously is prefered over a pathway with a nitrenium ion intermediate? (For the simultaneous pathway, the group in the anti-position with respect to the oxime hydroxyl will migrate. If the nitrenium ion forms, both group will have a good chance to migrate. - GS).