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For the NMR spectrum shown below*, draw the structure of the reactant next to the spectrum and label the protons so that they match the letter labels shown on the NMR spectrum. Fill in the Chemical shift, integration and multiplicity in the table. You may want to complete sections c) and d) before assigning the aromatic ring protons. There is a very broad (almost flat) signal here. 14 B Appears to be a singlet Integration - 1 A Integration = 2 HSP-04-502 STRUCTURE: 12 10 Proton label A B C D 8 0) с Integration = 2 D Broad singlet Integration - 2 N ppm Chemical shift Relative integration (ppm) Multiplicity

For the NMR spectrum shown below*, draw the structure of the reactant next to the spectrum and label the protons so that they match the letter labels shown on the NMR spectrum. Fill in the Chemical shift, integration and multiplicity in the table. You may want to complete sections c) and d) before assigning the aromatic ring protons. There is a very broad (almost flat) signal here. 14 B Appears to be a singlet Integration - 1 A Integration = 2 HSP-04-502 STRUCTURE: 12 10 Proton label A B C D 8 0) с Integration = 2 D Broad singlet Integration - 2 N ppm Chemical shift Relative integration (ppm) Multiplicity

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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This question deals with 4-aminobenzoic acid.

b. For the NMR spectrum shown below*, draw the structure of the reactant next to the spectrum and label the protons so that they match the letter labels shown on the NMR spectrum. Fill in the Chemical shift, integration and multiplicity in the table. You may want to complete sections c) and d) before assigning the aromatic ring protons. B C Integration=2 There is a very broad (almost flat) signal here. Appears to be a singlet Integration - 1 A = Integration 2 D Broad singlet Integration - 2 14 12 10 8 6 2 HSP-04-502 ppm Proton Chemical shift Relative integration Multiplicity STRUCTURE: label (ppm) A B C D
Transcribed Image Text:b. For the NMR spectrum shown below*, draw the structure of the reactant next to the spectrum and label the protons so that they match the letter labels shown on the NMR spectrum. Fill in the Chemical shift, integration and multiplicity in the table. You may want to complete sections c) and d) before assigning the aromatic ring protons. B C Integration=2 There is a very broad (almost flat) signal here. Appears to be a singlet Integration - 1 A = Integration 2 D Broad singlet Integration - 2 14 12 10 8 6 2 HSP-04-502 ppm Proton Chemical shift Relative integration Multiplicity STRUCTURE: label (ppm) A B C D
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