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.

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...

See similar textbooks

Similar questions

D10) The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this synthesis, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compound c.
3. Provide a complete, detailed and stepwise mechanism for the following acid catalyzed hydration reaction. In order to receive full credit, you must show all electron movement and provide all of the intermediates for this reaction. In addition, your intermediates must indicate proper stereochemistry where appropriate: لكم H₂O* HO
( plz complete the follow , do all plz as they are subpart)
3. Synthesize the compound shown below from bromobenzene using any other necessary reagents or solvents.
Please don't provide hand writtin solution....
What is the molality of the dentist's amalgam? Recall that the amalgam is 70% Hg and 30% Cu by mass
Please don't provide handwritten solution......
Give a clear explanation handwritten answer..give the mechanism of given bleow reactions
Please help me with the mechanism below: 1. Draw the mechanism for the reaction described here - preparation of (4-picolyl)-triphenylphosphonium Chloride. Reagents: 4-picolyl chloride (also known as 4-pyridylmethyl chloride and 4-(chloromethyl) pyridine), triphenylphosphine, dimethylformamide. Heat is used in this reaction (80 degrees Celsius).
Give answer all questions with explanation please
please answer parts a and b of the question with good explanation
4. Suggest how you would carry out each of these syntheses (remember, your target compound is the compound on the left – the compound you start with is the compound on the right. Br