Question: 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.

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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