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- What product is formed when each compound is treated first with LDA in THF solution at low temperature, followed by CH3CH2I ?The following isomerization reaction, drawn using D-glucose as starting material, occurs with all aldohexoses in the presence of base. Draw a stepwise mechanism that illustrates how each compound is formed. сно сно сно CH2OH C=0 H- OH H- -OH но- H- но H- "OH но H- Но H- но H- H- -H- H20 H- HO- O- H- -O- H- -OH -O- OH ČHOH CH,OH ČH2OH ČH2OH (recovered starting material) D-glucoseWhat enolate is formed when each ketone is treated with LDA in THF solution? What enolate is formed when these same ketones are treated with NaOCH3 in CH3OH solution?
- What product is formed when 2-acetylcyclopentanone is treated withNaOCH2CH3, followed by CH3I?Tamoxifen is a drug used to prevent and treat breast cancer. What are all the possible metabolic reactions for this drug? Aromatic hydroxylation Epoxidation ON-dealkylation Benzylic hydroxylation O Epoxidation followed by epoxide hydrolysisDraw the products formed (including stereoisomers) when each compound is reduced with NaBH4 in CH3OH.
- What product is formed when each compound is treated with either LiAlH4 (followed by H2O), or NaBH4 in CH3OH?Can you provide amechanism,conditions and reagents needed to reduce ketone and produce R confuguration of OH C c OH H HThe product of oxidation of 1-Hexanol with Dess-Martin Periodinane is: O AL Hexanal O B) 2 Hexanonc OC Hexanoic Acid DHexanC