Why would the alcohol in the following compound need to be protected before reaction? 
A) If it isn't protected,the product will be a carboxylic acid.
B) The Grignard reagent will react with the alcohol before the ketone.
C) Magnesium is Lewis acidic and will coordinate with the alcohol.
D) There is no need to protect the alcohol.
Correct Answer:
Verified
Q3: If a compound is reduced,what is the
Q4: Why are ketones less reactive than aldehydes?
A)Ketones
Q5: Which reagent can be used to reduce
Q10: What is the product of the following
Q11: Which reagent can be used to reduce
Q11: Rank the following compounds in order of
Q12: What is the name of the general
Q16: What is the name of the general
Q17: Which reagent can be used to reduce
Q20: What reagent would be used to reduce
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