1. The dibenzalacetone preparation reaction is almost all reversible. However, good product performance is easily obtained. Explain. 2. State why the reaction between acetone and 2-pentanone would not be a good method for preparing 4-methyl-3-hepten-2-one. 3. Write down the reaction of the congestion of benzaldehyde with acetophenone. 4. Suggest a way to modify the procedure used in the laboratory so that the reaction produces benzalacetone instead of dibenzalacetone
1. The dibenzalacetone preparation reaction is almost all reversible. However, good product performance is easily obtained....
Indicate why the reaction between acetone and 2-pentanone would not be a good method to prepare 4-methyl-3-hepten-2-one 3. Indique por qué la reacción entre acetona y 2-pentanona no sería un buen método para preparar 4-metil-3-hepten-2-ona.
Justify why 1. What is the product of the chromic acid oxidation of the compound shown in the box? 2. What is the product of reduction with excess lithium aluminum hydride, followed by medium treatment aqueous acid, of the compound shown in the box? 3. What is the product of the reaction with excess methyl magnesium bromide, followed by treatment in aqueous acidic medium, of the compound shown in the box? 1. ¿Cuál es el producto de la oxidación con...