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Alkenes can be converted to ethers by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called alkoxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl ether, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final ether 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.

Neutral product(s) of oxymercuration. Include stereoisomers, if any.Map MeOH, THF Ether product(s) of demercuration. Include stereoisomers, if any Select all that apply: The ether product(s) of the reaction is characterized as being NaBH4 □ R,S (and/or S,R). Ho □ achiral □ racemic. □ diastereomers. □R. S.

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Oxy mexeu ration - Demur curation Lelectrophilic addition 1. На-ОАс SP2 THỜ Na BHq (Reducing agent) Choh ? auti alcohol Racmi

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