Chemistry, 12.12.2020 17:10 darkshaders11

Starting with (2R,3R)-2-chloro-3,4-dimethylpentan e, a) draw the expected major product for each step, including regiochemical and stereochemical details when needed. In addition, b) briefly explain the mechanistic rationale for each transformation. i. t-BuOK/t-BuOH, heat
ii. MCPBA/CH2Cl2
iii. H3O

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Starting with (2R,3R)-2-chloro-3,4-dimethylpentan e, a) draw the expected major product for each step, including regiochemical and stereochemical details when needed. In addition, b) briefly explain the mechanistic rationale for each transformation. i. t-BuOK/t-BuOH, heat ii. MCPBA/CH2Cl2 iii. H3O

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Starting with (2R,3R)-2-chloro-3,4-dimethylpentan e, a) draw the expected major product for each step, including regiochemical and stereochemical details when needed. In addition, b) briefly explain the mechanistic rationale for each transformation. i. t-BuOK/t-BuOH, heat
ii. MCPBA/CH2Cl2
iii. H3O