One of the most important uses for Grignard reagents is their addition to carbonyl compounds to give new carbon-carbon bonds. In this reaction, the carbon of the organometallic compound acts as a nucleophile to add to the positive carbon of the carbonyl forming an alkoxide ion intermediate. Aqueous acid is used in the second step to protonate the alkoxide lon and form the product alcohol. yo 1. CH.MgBr 2. H₂O¹ 3 [References] OH Cots (racemic) Draw the structure of the product(s) of step 1 when the following compound reacts with phenylmagnesium bromide. 500.88 . You should include all products. • You do not have to consider stereochemistry. • Draw cations and anions in separate sketchers. Separate multiple products using the + sign from the drop-down menu.

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One of the most important uses for Grignard reagents is their addition to carbonyl compounds to give new carbon-carbon bonds. In this reaction, the carbon of the
organometallic compound acts as a nucleophile to add to the positive carbon of the carbonyl forming an alkoxide ion intermediate. Aqueous acid is used in the
second step to protonate the alkoxide lon and form the product alcohol.
yo
1. CH.MgBr
2.H₂0¹
OH
CoHs
68083
References)
(racemic)
Draw the structure of the product(s) of step 1 when the following compound reacts with phenylmagnesium bromide.
. You should include all products.
You do not have to consider stereochemistry.
.Draw cations and anions in separate sketchers.
Separate multiple products using the + sign from the drop-down menu.
Transcribed Image Text:One of the most important uses for Grignard reagents is their addition to carbonyl compounds to give new carbon-carbon bonds. In this reaction, the carbon of the organometallic compound acts as a nucleophile to add to the positive carbon of the carbonyl forming an alkoxide ion intermediate. Aqueous acid is used in the second step to protonate the alkoxide lon and form the product alcohol. yo 1. CH.MgBr 2.H₂0¹ OH CoHs 68083 References) (racemic) Draw the structure of the product(s) of step 1 when the following compound reacts with phenylmagnesium bromide. . You should include all products. You do not have to consider stereochemistry. .Draw cations and anions in separate sketchers. Separate multiple products using the + sign from the drop-down menu.
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