Please help! The Michael reaction is a conjugate addition reaction between a stable nucleophilic enolate ion (the donor) and an
α,β-unsaturated carbonyl compound (the acceptor). 1.) Draw the structure of the product of the Michael reaction between ethyl propenoate and 3-oxobutanenitrile.2.)The Michael reaction is a conjugate addition reaction between a stable nucleophilic enolate ion (the donor) and an α,β-unsaturated carbonyl compound (the acceptor). Draw the structure of the product of the Michael reaction between propenamide and 2,4-pentanedione.
1 answer:
Answer:
See explaination andd attachment
Explanation:
Treatment of aldehydes and ketones with a suitable base can lead to the formation of a nucleophilic species called an enolate that reacts with electrophiles. These C nucleophiles are useful for making new carbon-carbon bonds.
Please kindly see attachment for the drawings.
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