Draw 2 Neutral product(s) of oxymercuration. Clearly show stereochemistry. Hg (oоссH,), Н,О, THF Alcohol product(s) of demercuration. Include stereoisomers, if any. Select all that apply: The alcohol product(s) of the reaction is characterized as being R,R. NaBH R,S (and/or S,R) S,S Но- achiral racemic diastereomers R. S.

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Alkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.

Draw 2 Neutral product(s) of oxymercuration. Clearly show stereochemistry.
Hg (oоссH,),
Н,О, THF
Alcohol product(s) of demercuration. Include stereoisomers, if any.
Select all that apply: The alcohol product(s)
of the reaction is characterized as being
R,R.
NaBH
R,S (and/or S,R)
S,S
Но-
achiral
racemic
diastereomers
R.
S.
Transcribed Image Text:Draw 2 Neutral product(s) of oxymercuration. Clearly show stereochemistry. Hg (oоссH,), Н,О, THF Alcohol product(s) of demercuration. Include stereoisomers, if any. Select all that apply: The alcohol product(s) of the reaction is characterized as being R,R. NaBH R,S (and/or S,R) S,S Но- achiral racemic diastereomers R. S.
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