In previous syntheses involving equilibria (like the Fischer esterification), one reactant was used as a solvent to achieve maximum conversion of the other to product. In the case of our crossed aldol condensation, using acetone as the solvent is not expected to achieve the desired goal. Explain why this is so by hand-drawing the major product which may form from this week’s synthesis when a large excess of acetone is mixed with the other reagents at the start of the reaction.