Describe the mechanism step of this reaction below: H3O* OEt Explain the reason of the nucleophilic attack of Grignard reagent to the carbon which has ethoxy group rather than carbonyl. R.
Describe the mechanism step of this reaction below: H3O* OEt Explain the reason of the nucleophilic attack of Grignard reagent to the carbon which has ethoxy group rather than carbonyl. R.
Chapter24: Amines And Heterocycles
Section24.9: Heterocyclic Amines
Problem 22P
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![Describe the mechanism step of this reaction
below:
RMgBr,
H3O*
OEt
'R
Explain the reason of the nucleophilic attack of
Grignard reagent to the carbon which has ethoxy
group rather than carbonyl.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb203d6e4-a59c-4161-b407-fb34a849f237%2F5b97a730-02a4-4cfb-bc87-75ff6b5beef2%2Flzkxwe6_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Describe the mechanism step of this reaction
below:
RMgBr,
H3O*
OEt
'R
Explain the reason of the nucleophilic attack of
Grignard reagent to the carbon which has ethoxy
group rather than carbonyl.
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