In the aldol condensation reaction of a ketone with an aldehyde, both having acidic alpha hydrogens present; what is the major product?
Is it formed from enol of the ketone, or of the aldehyde? Is it from the enol of the ketone, because aldehydes are more reactive towards nucleophilic addition? Confirming, just to be sure.
Furthermore, which aldol condensation products are usually neglected?