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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

Draw the major products obtained from the reaction of one equivalent of HCl with the following compounds. For each reaction, indicate the kinetic and thermodynamic products.

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

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

A student obtained two products from the reaction of 1,3-cyclohexadiene with Br2 (disregarding stereoisomers). His lab partner was surprised when he obtained only one product from the reaction of 1,3-cyclohexadiene with HBr (disregarding stereoisomers). Account for these results.

a. Why does deuterium add to C-1 rather than to C-4 in the preceding reaction?

b. Why was DCl rather than HCl used in the reaction?

What are the products of the following reactions?

Classify the following species as aromatic, nonaromatic, or antiaromatic:
See all solutions

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