Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
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Chapter 30.8, Problem 9P

When a 2, 6-disubstituted allyl phenyl ether is heated in an attempted Claisen rearrangement, migration occurs to give the p-allyl product as the result of two sequential pericyclic reactions. Explain.

Chapter 30.8, Problem 9P, When a 2, 6-disubstituted allyl phenyl ether is heated in an attempted Claisen rearrangement,

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As we will learn in Chapter 9, an epoxide is an ether with an oxygen atom in a three-membered ring. Epoxides can be made by intramolecular SN2 reactions of intermediates that contain a nucleophile and a leaving group on adjacent carbons, as shown.Assume that each of the following starting materials can be converted to an epoxide by this reaction. Draw the product formed (including stereochemistry) from each starting material. Why might some of these reactions be more difficult than others in yielding nucleophilic substitution products?
Please provide the steps that each carbonation will undergo to form a carbonation that is more stable. Use arrows to explain the steps and provide the product for each.
Provide reagents/conditions to accomplish the following transformations. Label each reaction type in the steps you provide. OEt MeO OMe
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