Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s) or correct...

Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s) or correct vocabulary word/phrase to complete the description. If a specific stereoisomer (e.g single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g. lines not dashes).

If we used the reagent NaOH, H2O.

The major product is compound ________________ by a(n) ________________ mechanism.

On first inspection, compound ________________ appears incorrectly to be the major product, but it is prevented by difficulty getting into the ________________ transition state. If we want this compound we'd have to start with the (pick one: cis, trans) ________________ diastereomer of the original starting material.

If we convert the reagent to pure H2O.

The primary products of the reaction are compounds ________________ , ________________, and ________________

 which are formed by ________________ and ________________ mechanisms. These products form due to an extra ________________ step in the mechanism. If this extra step did not happen we'd see compounds ________________ , ________________ , and ________________ as products instead.

If we convert the reagent to first 1) CH3COONa, DMSO and then 2) NaOH, H2O:

Initially we'll form ________________ as the product after the first step by ________________ mechanism. Then we'll form the final product ________________ by a ________________ reaction.