Why can't you use acidic conditions (such as aqueous hydrochloric acid) for the addition of a Grignard reagent to a ketone?
A) Because the Grignard reagent will react with the acid and be quenched
B) Because the ketone will be protonated and thus unreactive
C) Because the ketone will form an unreactive enol
D) Because the Grignard reagent won't dissolve in aqueous solutions
Correct Answer:
Verified
Q5: Why are strongly acidic conditions not used
Q6: What is the IUPAC name for the
Q7: What is the first step in nucleophilic
Q8: Is the following reaction reversible and,if so,under
Q9: Using 1H NMR spectroscopy,how can you tell
Q11: What is the product of the following
Q12: What is the product of the following
Q13: What is the product of the following
Q14: What is the major organic product obtained
Q15: Using IR spectroscopy,how can you tell the
Unlock this Answer For Free Now!
View this answer and more for free by performing one of the following actions
Scan the QR code to install the App and get 2 free unlocks
Unlock quizzes for free by uploading documents