Chapter 15: Q87P (page 737)
Question: What product do you expect to obtain from each of the following reactions?
a.
b.
Short Answer
Answer
a.
b.
Chapter 15: Q87P (page 737)
Question: What product do you expect to obtain from each of the following reactions?
a.
b.
Answer
a.
b.
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Get started for freeWhen a compound with molecular formula undergoes acid-catalyzed hydrolysis, one of the products that is isolated gives the following NMR spectrum. Identify the compound.
An aqueous solution of a primary or secondary amine reacts with an acyl chloride to form an amide as the major product. However, if the amine is tertiary, an amide is not formed. What product isformed? Explain.
Write the mechanism for the acid-catalyzed reaction of an amide with an alcohol to form an ester.
a. Propose a mechanism for the reaction of acetic anhydride with water.
b. How does this mechanism differ from the mechanism for the reaction of acetic anhydride with an alcohol?
If propionyl chloride is added to one equivalent of methylamine, only a 50% yield of N-methylpropanamide is obtained. If, however, the acyl chloride is added to two equivalents of methylamine, the yield of N-methylpropanamide is almost 100%. Explain these observations.
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