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.

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.

periodic trends is an atom that gets larger as the number of electronic shells increase, the radius of atoms increases as you go down a certain group in the periodic table of elements. in general, the size of an atom will decrease as you move from left to right of a certain period.