For each of the compounds A and B do the following: (i) Sketch the NMR spectrum that you would expect for each compound. In your sketch show the approximate position of the signal for each type of proton in the molecule, show its splitting and over the signal write the expected value of the integration. (ii) List what you expect to be two major IR signals for each compound and identify what functional group or bond would be giving each signal.
For each of the compounds A and B do the following: (i) Sketch the NMR spectrum that you would expect for each compound. In your sketch show the approximate position of the signal for each type of proton in the molecule, show its splitting and over the signal write the expected value of the integration. (ii) List what you expect to be two major IR signals for each compound and identify what functional group or bond would be giving each signal.
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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For each of the compounds A and B do the following:
-
(i) Sketch the NMR spectrum that you would expect for each compound. In your sketch show the approximate position of the signal for each type of proton in the molecule, show its splitting and over the signal write the expected value of the integration.
-
(ii) List what you expect to be two major IR signals for each compound and identify what functional group or bond would be giving each signal.
Transcribed Image Text:CH3
CH3CH₂-O-CH₂-C=N
B
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Step 1: Basic discussion
VIEWStep 2: Finding out H-NMR signals for compound A
VIEWStep 3: H-NMR spectrum for compound A
VIEWStep 4: Major IR signals for compound A
VIEWStep 5: Finding out H-NMR signals for compound B
VIEWStep 6: H-NMR spectrum for compound B
VIEWStep 7: Major IR signals for compound B
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