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Methyl p-Nitrobenzoate

Methyl p-Nitrobenzoate

Chemistry
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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2. In Experiment 4B, it was shown from the NMR spectrum that the meta-di-substituted Nitration product had been recorded as a major product: COOME COOME HNO3 H,SO, NO2 Major product However, there were two other possible but less favorable routes, i.e. ortho- or para- positions for the nitronium to attack the aromatic ring with. Draw the H-NMR spectrum for Methyl p-Nitrobenzoate in case the substitution takes place at the para-position. Pay attention to the chemical shift, the splitting pattern, and approximate the integration in your spectra. Methyl p-Nitrobenzoate 3.0 2.5 2.0 1.5 - 1.0- 0.5 4 3. 2 1. 10 6. 8.
Transcribed Image Text:2. In Experiment 4B, it was shown from the NMR spectrum that the meta-di-substituted Nitration product had been recorded as a major product: COOME COOME HNO3 H,SO, NO2 Major product However, there were two other possible but less favorable routes, i.e. ortho- or para- positions for the nitronium to attack the aromatic ring with. Draw the H-NMR spectrum for Methyl p-Nitrobenzoate in case the substitution takes place at the para-position. Pay attention to the chemical shift, the splitting pattern, and approximate the integration in your spectra. Methyl p-Nitrobenzoate 3.0 2.5 2.0 1.5 - 1.0- 0.5 4 3. 2 1. 10 6. 8.
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