(a)
Interpretation: The product formed by the hydrolysis of given compound is to be determined.
Concept introduction:
(b)
Interpretation: The product formed by the hydrolysis of given compound is to be determined.
Concept introduction: Aldehyde or ketone on reaction with secondary amine forms enamine. The nucleophilic attack of secondary amine on carbonyl carbon results in the formation of intermediate carbinolamine. This intermediate loses water to form an enamine. In this case the elimination occurs across two adjacent carbon atoms to form new carbon-carbon double bond.
(c)
Interpretation: The product formed by the hydrolysis of given compound is to be determined.
Concept introduction: Aldehyde or ketone on reaction with secondary amine forms enamine. The nucleophilic attack of secondary amine on carbonyl carbon results in the formation of intermediate carbinolamine. This intermediate loses water to form an enamine. In this case the elimination occurs across two adjacent carbon atoms to form new carbon-carbon double bond.
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Chapter 18 Solutions
Organic Chemistry (6th Edition)
- Can you List and number the necessary reagents needed for each reactionarrow_forwardAnswer the following questions about atomoxetine, a drug used to treatattention deficit hyperactivity disorder (ADHD). a.) What amides can be reduced to form atomoxetine?b.) What starting materials can be used to form atomoxetine by reductiveamination? Draw all possible methods.c.) What products are formed by Hofmann elimination of atomoxetine?arrow_forwardWhat amine is formed by reduction of each amide?arrow_forward
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- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
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