1. Draw the general reaction that occurs between benzaldehyde and acetophenone and propose a mechanism for the formation of chalcones from these reagents in the presence of NaOH.
2.
a. Why does the enolate ion preferentially react with the benzaldehyde and not with the acetophenone in this reaction?
b. Briefly explain the advantages of eliminating the reaction solvent.
c. Can you think of any complications that may result as a consequence of eliminating the reaction solvent?
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