The following substances can be prepared by a nucleophilic addition reaction between an aldehyde or ketone and a nucleophile. Identify the reactants from which they were prepared. If the substance is an acetal, identify the carbonyl compound and the alcohol; if it is an imine or enamine, identify the carbonyl compound and the amine. You do not have to consider stereochemistry. In cases where there is more than one answer, just give one. Use Grignard reagents when an organometallic reagent is required. Draw the Grignard reagent as a covalent magnesium bromide. LOH OH 888

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The following substances can be prepared by a nucleophilic addition reaction between an aldehyde or ketone
and a nucleophile. Identify the reactants from which they were prepared. If the substance is an acetal, identify
the carbonyl compound and the alcohol; if it is an imine or enamine, identify the carbonyl compound and the
amine. You do not have to consider stereochemistry. In cases where there is more than one answer, just give
one. Use Grignard reagents when an organometallic reagent is required. Draw the Grignard reagent as a
covalent magnesium bromide.
LOH
OH
888
Transcribed Image Text:The following substances can be prepared by a nucleophilic addition reaction between an aldehyde or ketone and a nucleophile. Identify the reactants from which they were prepared. If the substance is an acetal, identify the carbonyl compound and the alcohol; if it is an imine or enamine, identify the carbonyl compound and the amine. You do not have to consider stereochemistry. In cases where there is more than one answer, just give one. Use Grignard reagents when an organometallic reagent is required. Draw the Grignard reagent as a covalent magnesium bromide. LOH OH 888
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