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Acid Chloride to Ketone
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Acid Chloride to Ketone
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21. Aldehydes and Ketones: Nucleophilic Addition / Acid Chloride to Ketone / Problem 3
Problem 3
Why do organometallics often react twice with acid chlorides, resulting in disubstituted alcohols rather than ketones?
A
Because they form stable intermediates that resist further reaction
B
Because they lack sufficient reactivity to stop at the ketone stage
C
Because they are highly reactive and continue to attack the formed ketone
D
Because they only react with the ester group within acid chlorides
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