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 CaH2N2 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.

Benzimidazole is a fused ring in which benzene and imidazole are fused together. It is a heterocyclic aromatic compound containing Nitrogen atoms. It has acidic protons . It reacts with strong base n-BuLi and abstracts the proton form nitrigen at position-1. After that it reacts with Benzyl bromide in Polar aprotic solvent DMSO via SN2 (bimolecular nucleophilic substitution).

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Chemistry

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 CaH2N3 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.

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 CaH2N3 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.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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