Stereochemical Outcomes in Transformations
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What is the absolute stereochemistry of the asymmetric carbon in compound O? When compound O is treated with lithium diisopropyl amide, followed by allyl bromide, compound P is produced as a single stereoisomer. What is the absolute stereochemistry of the newly produced asymmetric carbon in P? Provide concise explanations for the stereochemical outcomes observed in the O to P and P to Q transformations.
See the attached file.
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Please refer to attachment.
i) Lithium coordination between the two oxygens gives you a rigio enolate
ii) The double bond of the enolate has two faces: one above and one below the place of the page. The bottom face of ...
Solution Summary
The solution is provided in an attachment regarding stereochemical outcome in transformations.
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