Explain how the class I carbonyl compound reacts?What will be the product when ethylamine and propyl amine reacts with acetyl chloride?Why only one amide obtained after the reaction of acetyl chloride with a mixture of ethylamine and trimethylamine? Excess amine is required in the reaction of acetyl chloride with amine whereas excess alcohol is not required in the reaction of acetyl chloride and alcohol. Why?List the following ester in order of decreasing reactivities towards hydrolysis with reason:Methyl benzoate, p-nitro methyl benzoate and p-methoxy methyl benzoate

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Answered: Explain how the class I carbonyl

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section: Chapter Questions

Problem 19.57P

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Explain how the class I carbonyl compound reacts?
What will be the product when ethylamine and propyl amine reacts with acetyl chloride?
Why only one amide obtained after the reaction of acetyl chloride with a mixture of ethylamine and trimethylamine?
Excess amine is required in the reaction of acetyl chloride with amine whereas excess alcohol is not required in the reaction of acetyl chloride and alcohol. Why?
List the following ester in order of decreasing reactivities towards hydrolysis with reason:

Methyl benzoate, p-nitro methyl benzoate and p-methoxy methyl benzoate

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