3. If your product from this experiment (benzimidazole) is treated with a strong base (nBuLi) followed bybenzyl bromide (Ph-CH2-Br) in a polar aprotic solvent like DMSO, a molecule C4H12N, is formed. Pleasedraw a reaction scheme of the overall sequence (including the structure of the product), and also anelectron-pushing mechanism for each of the reactions that take place.

Answered: Image /qna-images/answer/f3e43fba-01ca-47e0-98cc-d744b09c52d6.jpg

3. If your product from this experiment (benzimidazole) is treated with a strong base (nBuLi) followed by benzyl bromide (Ph-CH2-Br) in a polar aprotic solvent like DMSO, a molecule CaH12N; is formed. Please draw a reaction scheme of the overall sequence (including the structure of the product), and also an electron-pushing mechanism for each of the reactions that take place.

3. If your product from this experiment (benzimidazole) is treated with a strong base (nBuLi) followed by benzyl bromide (Ph-CH2-Br) in a polar aprotic solvent like DMSO, a molecule CaH12N; is formed. Please draw a reaction scheme of the overall sequence (including the structure of the product), and also an electron-pushing mechanism for each of the reactions that take place.

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

Chapter19: Enolate Anions And Enamines

Section19.9: Crossed Enolate Reactions Using Lda

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