Talk:Mod:cg507

1.2.1 Cp dimers: jmols? Why is the endo isomer preferred? Why is product 4 preferred? Where is your analysis?

1.2.2 NAD: Sterics are the reason the Grignard reagent attacks on the same side as the carbonyl group? So the carbonyl is on one (unspecified) side of the molecule, why does attack happen on face side only and which face? You do not seem to have put any thought into this.

1.2.3 Taxol: For an explanation of hyperstable alkenes, you have told me to look at an article in JACS?

1.3.1 Carbene: Why does one alkene have a higher electron density than the other?

Mini-project: Lacking any real analysis.

Overall: Where were the jmols?!?! This really didn’t help me assess your structures. And where was your analysis? This is sloppy work.