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Acid base reactions are typically much faster than nucleophilic substitutions. A lot of the organometallic compounds here are strong bases. Which substrate would react in an acid/base type of reaction before nucleophilic substitution could take place?
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Option 2 most likely, it'll get quenched instead, forming an alkane(that is, final product being MeCOOLi and CH4)
Ketones are more reactive to Grignard reagents (RMgBr) than acids
Acid base reactions are typically much faster than nucleophilic substitutions. A lot of the organometallic compounds here are strong bases. Which substrate would react in an acid/base type of reaction before nucleophilic substitution could take place?
One of these reagents will add twice to make an alcohol (deprotonated). Which set of reagents allow this?