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
Chapter9: Alkynes: An Introduction To Organic Synthesis
Section9.SE: Something Extra
Problem 49AP: Occasionally, a chemist might need to invert the stereochemistry of an alkene—that is, to convert...
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Refer to image, answer all parts and explain. Will rate!
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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