6. Ester Hydrolysis Mechanism: Draw the proper FULL electron-pushing mechanism for the reaction below, including ALL intermediates (with formal charges) and electron pushing arrows. Label the Electrophile and Nucleophile in each step! OH 7. Amide Formation Mechanism: Draw the proper FULL electron-pushing mechanism for the reaction below to synthesize Lidocaine, including ALL intermediates (with formal charges) and electron pushing arrows. Label the Electrophile and Nucleophile in each step! Use the synthesis of DEET in your notes to help you, it's the same mechanism. NH NH, 2.

6. Ester Hydrolysis Mechanism: Draw the proper FULL electron-pushing mechanism for the reaction below, including ALL intermediates (with formal charges) and electron pushing arrows. Label the Electrophile and Nucleophile in each step! OH 7. Amide Formation Mechanism: Draw the proper FULL electron-pushing mechanism for the reaction below to synthesize Lidocaine, including ALL intermediates (with formal charges) and electron pushing arrows. Label the Electrophile and Nucleophile in each step! Use the synthesis of DEET in your notes to help you, it's the same mechanism. NH NH, 2.

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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Please help me with these. The blank at the bottom could possibly be no reaction.
what did i do wrong here. , it seems to be marking it wrong but i thought it needed to be protonated
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