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Chapter 24: Q.14. (page 962)

Question: What cyclic product is formed when each 1,5-dicarbonyl compound is treated with aqueous $O H$ ?

Short Answer

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Answer

Step by step solution

Dehydration reaction

The removal of water from a compound yields alkene. This reaction is termed a dehydration reaction.

Formation of products

a. The reaction is shown below:

Product formation in a

b. The reaction is shown below:

Product formation in b

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Most popular questions from this chapter

Question: 2-Pentylcinnamaldehyde, commonly called flosal, is a perfume ingredient with a jasmine-like odor. Flosal is an $α, β$ -unsaturated aldehyde made by a crossed aldol reaction between benzaldehyde $(C_{6} H_{5} C H O)$ and heptanal $(C H_{3} C H_{2} C H_{2} C H_{2} C H_{2} C H_{2} C H O)$ , followed by dehydration. Draw a stepwise mechanism for the following reaction that prepares flosal.

Question:What starting materials are needed to prepare each compound using a Michael reaction?

Question: 4-Methylpyridine reacts with benzaldehyde $(C_{6} H_{5} C H O)$ in the presence of a base to form A.

(a) Draw a stepwise mechanism for this reaction.

(b) Would you expect 2-methylpyridine or 3-methylpyridine to undergo a similar type of condensation reaction? Explain why or why not.

Question: Which carbonyl compounds do not undergo an aldol reaction when treated with OH^- in H₂O ?

Question: Draw the product formed from an aldol reaction with the given starting material(s) using $O H, H_{2} O$ .

See all solutions

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Question: What cyclic product is formed when each 1,5-dicarbonyl compound is treated with aqueous OH?

Short Answer

Step by step solution

Dehydration reaction

Formation of products

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Most popular questions from this chapter

Recommended explanations on Chemistry Textbooks

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Question: What cyclic product is formed when each 1,5-dicarbonyl compound is treated with aqueous $O H$ ?