Rank the following proton descriptions for the major methyl nitrobenzoate product. H O₂N. OCH 3 * H H Most Deshielded (Down Field) 1 2 3 4 H 5 The proton in between the two EWGs and only experiencing long-range coupling. The proton next to the strong deactivator nitro group and experiencing three-bond coupling with a neighboring aromatic proton. The proton next to the moderate deactivator ester group and experiencing three-bond coupling with a neighboring aromatic proton. The proton meta to the two EWGs on the aromatic ring and experiencing three-bond coupling with two neighboring aromatic protons. The methyl group protons of the ester substituent. Most Shielded (Up Field)

Rank the following proton descriptions for the major methyl nitrobenzoate product. H O₂N. OCH 3 * H H Most Deshielded (Down Field) 1 2 3 4 H 5 The proton in between the two EWGs and only experiencing long-range coupling. The proton next to the strong deactivator nitro group and experiencing three-bond coupling with a neighboring aromatic proton. The proton next to the moderate deactivator ester group and experiencing three-bond coupling with a neighboring aromatic proton. The proton meta to the two EWGs on the aromatic ring and experiencing three-bond coupling with two neighboring aromatic protons. The methyl group protons of the ester substituent. Most Shielded (Up Field)

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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