Talk:Module1:doushinidecuoqingyiaishangwo

1.2.1 Cp Dimers: Well layed out and clearly stated answer, good work! Nice to see Jmol structures. The individual energy contributions for 3/4 are actually different enough for a comparison to be made. Relating these contributions to structural features of the molecules actually allows us to determine the reasons behind kinetic/thermodynamic selectivity. What do you think these would be? Of note, it's rather odd to give energies for MM calculations in Hartrees. In the future, you probably don't have to bother.

1.2.2 NAD: Answer is largely fine.

1.2.3 Taxol: An explanation as to the origin of hyperstability would have been welcome. Exactly what particular structural features of the alkene make it hyperstable?

1.3.1 Carbene: Pi orbital, not pie! Nice discussion on reactivity. Could have used a little more when discussing the IR stretches, particularly in relating them to your answer on the reactivity.

Mini-Project: Never use wikipedia as a reference! No matter what for, ever! Website referencing shold be avoided at all costs and if you have to reference a website make sure you indluce the date and time you last visited it. Good choice of molecule though. Although it is good to quantitatively compare the calculated and literature spectra, it is often more helpful to compare the deviations themselves (bar charts are particularly useful here). A little lacking in analysis, otherwise good.