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Chapter 8: Q31P (page 350)

What products would be obtained from the reaction of 1,3,5-hexatriene with one equivalent of HBr? Disregard stereoisomers.

Short Answer

Expert verified

First HBr breaks into H+ and Br-where it will do markoniv addition.

But here three double bond are present so these ions can attach with any double bond. So here three products will form.

Step by step solution

01

How reaction proceed

First HBr breaks into H+ and Br-where it will do markoniv addition.

But here three double bond are present so these ions can attach with any double bond. So here three products will form.

02

Final answer

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Most popular questions from this chapter

Rank the indicated hydrogen in the following compounds from most acidic to least acidic:

What diene and what dienophile should be used to synthesize the following?

Which of the following compounds could be protonated without destroying its aromaticity?

The heat of hydrogenation of 2,3-pentadiene, a cumulated diene, is 70.5 kcal/mol. What are the relative stabilities of cumulated, conjugated, and isolated dienes?

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a. 2,3-dimethyl-1,3-pentadiene

b. 2,4-dimethyl-1,3-pentadiene
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