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- Define Dehydration of the Aldol Product ?Draw structures for the carbonyl electrophile and enolate nucleophile that give the enone presentedBenzalacetone is a side product formed in the aldol condensation of dibenzalacetone. Show the reaction mechanism of how this side product, Benzalacetone, is formed.
- Write the structure(s) for the aldehyde(s) and/or ketone(s) that undergo an aldol addition reaction to form the product shown here. OH 2 HDraw the structure of the aldol that will form when cyclohexanone reacts with one mole ofbenzaldehyde. What is the name of this compound?1. Each of the following compounds can be prepared by a mixed aldol condensation reaction. Give the structures of the aldehyde and/or ketone precursors for each aldol product shown. so
- Give the products of the following substitution reactions. For every reaction, show electron pairs on both nucleophile and leaving group.Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below.Assume that attached starting materials can be converted to an epoxide by this reaction. Draw the product formed (including stereochemistry) from each starting material. Why might some of these reactions be more difficult than others in yielding nucleophilic substitution products?