Chapter 23: Q18P (page 773)
How would you prepare the following compound using a Michael reaction?
Short Answer
By the reaction between pent-1-ene-3-one and nitroethane we can prepare the given compound.
Chapter 23: Q18P (page 773)
How would you prepare the following compound using a Michael reaction?
By the reaction between pent-1-ene-3-one and nitroethane we can prepare the given compound.
All the tools & learning materials you need for study success - in one app.
Get started for freeEthyl dimethyl acetoacetate reacts instantly at room temperature when treated with ethoxide ion to yield two products, ethyl acetate, and ethyl 2-methyl propanoate. Propose a mechanism for this cleavage reaction.
What enone product would you expect from aldol condensation of each of the following compounds?
What product would you expect to obtain from the base treatment of 1,6-cyclo-decanedione?
Propose a mechanism to account for the following reaction of an enamine with an alkyl halide:
Cinnamaldehyde, the aromatic constituent of cinnamon oil, can be synthesized by mixed aldol condensation. Show the starting materials you would use, and write the reaction.
What do you think about this solution?
We value your feedback to improve our textbook solutions.