When (R)-3-buten-2-ol is treated with a peroxy acid, two stereoisomeric epoxides are formed in a 60:40 ratio.

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When (R)-3-buten-2-ol is treated with a peroxy acid, two stereoisomeric epoxides are formed in a 60:40 ratio. The minor stereoisomer has the structure shown.

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Organic Chemistry

ISBN: 978-0072905014

4th edition

Authors: Francis A. Carey

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Question Posted: Nov 17, 2009 05:37 AM

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When (R)-3-buten-2-ol is treated with a peroxy acid, two stereoisomeric epoxides are formed in a 60:40 ratio.

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a Oxygen may be transferred to either the front face or the back face of the double bond when R...View the full answer

Organic Chemistry

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