5. Treating y-butyrolactone with two equivalents of methylmagnesium bromide, followed by hydrolysis in aqueous acid, gives a compound with the molecular formula CçH1402, as shown below. Propose a structural formula for this compound, and show using curly arrows the reaction mechanism. 1. CH,MgBr (2 equiv.) 2. H*/H,O y-butyrolactone
5. Treating y-butyrolactone with two equivalents of methylmagnesium bromide, followed by hydrolysis in aqueous acid, gives a compound with the molecular formula CçH1402, as shown below. Propose a structural formula for this compound, and show using curly arrows the reaction mechanism. 1. CH,MgBr (2 equiv.) 2. H*/H,O y-butyrolactone
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter9: Nucleophilic Substitution And Β-elimination
Section: Chapter Questions
Problem 9.16P: Treatment of 1-aminoadamantane, C10H17N, with methyl 2,4-dibromobutanoate in the presence of a...
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![5. Treating y-butyrolactone with two equivalents of methylmagnesium bromide, followed by
hydrolysis in aqueous acid, gives a compound with the molecular formula CçH1402, as shown
below. Propose a structural formula for this compound, and show using curly arrows the reaction
mechanism.
1. CH,MgBr (2 equiv.)
2. H*/H,O
y-butyrolactone](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fed34bc7e-37d9-48ae-b1da-6d6b5245fe89%2Fe894addf-c5ea-457e-804e-8d54901aa10a%2Fazshx1ma.png&w=3840&q=75)
Transcribed Image Text:5. Treating y-butyrolactone with two equivalents of methylmagnesium bromide, followed by
hydrolysis in aqueous acid, gives a compound with the molecular formula CçH1402, as shown
below. Propose a structural formula for this compound, and show using curly arrows the reaction
mechanism.
1. CH,MgBr (2 equiv.)
2. H*/H,O
y-butyrolactone
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