Practice Problem: Crossed Aldol Products

The video tutorial explains the aldol condensation reaction involving acetone and a two-carbon aldehyde in the presence of sodium hydroxide. It covers the formation of enolates from both aldehyde and acetone, leading to four possible aldol condensation products. The tutorial emphasizes the concept of crossed aldol reactions, where both compounds can act as nucleophiles and electrophiles, resulting in different products. The video also provides insights into the mechanisms of these reactions, highlighting the role of alpha protons and the formation of new carbon-carbon bonds.

What new insight or understanding did you gain from this video?

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