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Chapter 7: Q36P (page 315)

Draw the mechanism for the following reaction

Short Answer

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Step by step solution

01

Step 1:

Addition of Br₂ to the triple bond in the presence of H₂O forms an enol that immediately tautomerizes to a ketone.

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Most popular questions from this chapter

Which alkyne would be the best one to use for the synthesis of each of the following ketones?

What is each compound’s systematic name?

Draw all the enol tautomers for each of the ketones in Problem 15.

What reagents would you use for the following synthesis?

a. (Z)-3-hexene from 3-hexyne

b. (E)-3-hexene from 3-hexyne

c. hexane from 3-hexyne

Which carbocation is more stable?

See all solutions

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