Predict the major organic product(s) of each reaction below. For reagents over the arrow, assume there is an excess of reagent. Be precise in your answer and pay particular attention to stereochemistry when appropriate., 8. h. j. 1. 03, CH₂Cl2, -78 °C 2. S(CH3)2, CH₂Cl2 -78-23 °C H3CO OH (hv high energy light) 1. CH₂l2, Zn/Cu Et₂0, 30 °C 2. MeSO₂Cl, pyridine 3. t-BuOK, t-BuOH HBr, hv стводан 1. Mg, THF 2. D₂0 1. KMnO4, H₂O, KOH acetone 2. HglO, HOẶc

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Predict the major organic product(s) of each reaction below. For reagents over the arrow, assume
there is an excess of reagent. Be precise in your answer and pay particular attention to
stereochemistry when appropriate..
f.
g.
h.
i.
j.
1. 03, CH₂Cl₂, -78 °C
2. S(CH3)2, CH₂Cl₂
-78-23 °C
H₂CO
OH
(hv high energy light)
1. CH₂l2, Zn/Cu
Et₂0, 30 °C
HBr, hv
словдань
. Br
2. MeSO₂Cl, pyridine
3. t-BuOK, t-BuOH
1. Mg, THF
2. D₂0
1. KMnO4, H₂O, KOH
acetone
2. HylOs, HOAC
Transcribed Image Text:Predict the major organic product(s) of each reaction below. For reagents over the arrow, assume there is an excess of reagent. Be precise in your answer and pay particular attention to stereochemistry when appropriate.. f. g. h. i. j. 1. 03, CH₂Cl₂, -78 °C 2. S(CH3)2, CH₂Cl₂ -78-23 °C H₂CO OH (hv high energy light) 1. CH₂l2, Zn/Cu Et₂0, 30 °C HBr, hv словдань . Br 2. MeSO₂Cl, pyridine 3. t-BuOK, t-BuOH 1. Mg, THF 2. D₂0 1. KMnO4, H₂O, KOH acetone 2. HylOs, HOAC
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