consider the following synthesis: HN HN -OH N H₂SO4 H₂O, heat || Excessive hydrolysis and heating yields the product II;

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Consider The Following Synthesis Hn Hn Oh N H So4 H O Heat Excessive Hydrolysis And Heating Yields The Product Ii 1 (126.14 KiB) Viewed 55 times

consider the following synthesis: HN HN -OH N H₂SO4 H₂O, heat || Excessive hydrolysis and heating yields the product II; what is its identity? NH₂ you HN OH HN HN A. HN B. C. Select the structure of the product in the following reaction. ΝΗ s Mild acid heat A. B. صل C. D. NH₂ D. Sodium borohydride, via nucleophilic addition, converts acetoacetic acid into which product? NaBH3 OH OH OH OH AGOH BOH OH Dhom A. B. C. D. OH Why is an amide less reactive to nucleophilic acyl substitution than an acid chloride? O A) Chloride is a better leaving group. O B) Nitrogen is better at donating electron density into the carbonyl with added resonance stability. OC) Chloride is a better leaving group and nitrogen is better at donating electron density into the carbonyl with added resonance stability. O D) The amide anion is less basic.