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d. CH2OH H2 Pd/C (a catalyst) `CH3 е. CH3 i) R2BH H3C ii) NaOH, HOOH Note: The reagent in step ii) is a separate oxidation step, not a work-up. Please refer to the 07-28-2021 lecture. f. Br2 CH3OH

d. CH2OH H2 Pd/C (a catalyst) `CH3 е. CH3 i) R2BH H3C ii) NaOH, HOOH Note: The reagent in step ii) is a separate oxidation step, not a work-up. Please refer to the 07-28-2021 lecture. f. Br2 CH3OH

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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01. Give the expected major product or products in each of the following electrophilic addition transformations. Clearly show stereochemistry where appropriate (e.g., by using wedged or dashed bond lines, or by writing axial or equatorial bonds). If no reaction is expected, write "NR". In cases where a chiral product is formed, only one enantiomer of the racemic mixture needs to be showRKI pts) а. W I WA - d. CH2OH H2 Pd/C (a catalyst) CH3 е. CH3 i) R2BH H3C i) NaOH, HOOН Note: The reagent in step ii) is a separate oxidation step, not a work-up. Please refer to the 07-28-2021 lecture. f. Br2 CH3OH
Transcribed Image Text:01. Give the expected major product or products in each of the following electrophilic addition transformations. Clearly show stereochemistry where appropriate (e.g., by using wedged or dashed bond lines, or by writing axial or equatorial bonds). If no reaction is expected, write "NR". In cases where a chiral product is formed, only one enantiomer of the racemic mixture needs to be showRKI pts) а. W I WA - d. CH2OH H2 Pd/C (a catalyst) CH3 е. CH3 i) R2BH H3C i) NaOH, HOOН Note: The reagent in step ii) is a separate oxidation step, not a work-up. Please refer to the 07-28-2021 lecture. f. Br2 CH3OH
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