Bromination of (Z)-3-hexene yields racemic 3,4-dibromohexane. Provide a detailed mechanism for formation of the (3S,4S)-enantiomer, specifically showing Br₂ addition occurring from the top face of the alkene. Part 1 out of 2 Ľ 2 attempts left Br edit structure... Br₂ X Check my work (35.45.)-dibromohexane Br edit structure... (3R, 4R,)-dibromohexane Next part Br CH3 Br Br2₂ Br+ HBr

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Bromination of (Z)-3-hexene yields racemic 3,4-dibromohexane. Provide a detailed mechanism for
formation of the (3S,4S)-enantiomer, specifically showing Br₂ addition occurring from the top face of
the alkene.
H
H
X-
Part 1 out of 2
Br -Br
edit structure ...
2 attempts left
Br₂
Check my work
(35.45.)-dibromohexane
Br
edit structure ...
(3R, 4R,)-dibromohexane
Next part
Br
CH3Br
Br₂
Br+
HBr
Transcribed Image Text:Bromination of (Z)-3-hexene yields racemic 3,4-dibromohexane. Provide a detailed mechanism for formation of the (3S,4S)-enantiomer, specifically showing Br₂ addition occurring from the top face of the alkene. H H X- Part 1 out of 2 Br -Br edit structure ... 2 attempts left Br₂ Check my work (35.45.)-dibromohexane Br edit structure ... (3R, 4R,)-dibromohexane Next part Br CH3Br Br₂ Br+ HBr
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