Predict the product(s) for the following reaction.           

Bonus question Provide an efficient stepwise synthesis for the following.             The answer should be entered as in the following example: (this is an example!) 1. NaNH2   2. CH3CH2Br   3. H2, Lindlar’s Cat.    4. BH3, THF   5. H2O2, NaOH                          (Keep three spaces between each step) All chemicals and reagents  structures should be correct and with the proper sequence. No partial credit.

Which of the following ketones cannot be prepared using an acetoacetic ester synthesis?

Provide the reactants necessary to prepare the following compound using Robinson annulation.      

Identify the product obtained in the hydrolysis of the following cyclic acid anhydride.

Which of the following compounds is most basic?

Which one of the following esters cannot form an enolate ion?

Which of the following reactions would not yield isopropyl acetate as major product?

What is the structure for ethyl 4-chlorobenzoate?

Which of the following compounds is an enol of compound X drawn below?