Talk:Organic:Alexandra
Cyclopentadiene: Good results. You could have made more of kinetic vs thermodynamic control in the discussion, and analyse how you might address the issue.
Prolinol: Good results, but since you did not include any 3D models, its difficult to tell what your conformations are, especially the second system. A dihedral of eg 125 is no good unless a clear definition of it is provided (or a 3D model).
Taxol: I can sort of find results for 9, but cannot see 10 mentioned anywhere? As far as I can see, the energy you report is actually for 10, not 9! I was confused here.
Dichlorocarbene. Your LUMO and particularly LUMO+1 look quite wrong (the latter should be oriented along the C-Cl bond and it clearly is not). You quote this interaction, but your results do not bear it out. If you get funny results for one method, try another method! A lot of discussion about basis sets in the vibrational section could probably be omitted. Good results, reasonable discussion.
Project: You appear to have forgotten the results for cyclopentadiene, since here too MM2 predicts the exo to be more stable. What about the energy difference at the MPW1PW91 DFT level? You do not appear to report this one! 13C: Did you apply an ester/amide correction to your results (mentioned in the instructions)? Lots of good effort in this project (you probably did more than was really expected).