. Associate the diagnostic peaks in the IR with functional groups, and assign the signals in the NMR to specific protons. Use this information to deduce the structures of your compounds. 1.4 1.3 1.2 Figure 5. NMR spectrum (300 MHz) of ethyl (R)-3-hydroxybutanoate, with chiral shift reagent added. 1.404 1.383 1.315 1.292 1.267
. Associate the diagnostic peaks in the IR with functional groups, and assign the signals in the NMR to specific protons. Use this information to deduce the structures of your compounds. 1.4 1.3 1.2 Figure 5. NMR spectrum (300 MHz) of ethyl (R)-3-hydroxybutanoate, with chiral shift reagent added. 1.404 1.383 1.315 1.292 1.267
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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Give answer all questions with explanation
![. Associate the diagnostic peaks in the IR with functional groups, and assign the
signals in the NMR to specific protons. Use this information to deduce the
structures of your compounds.
1.4
1.3
1.2
Figure 5. NMR spectrum (300 MHz) of ethyl (R)-3-hydroxybutanoate, with chiral shift
reagent added.
1.404
1.383
1.315
1.292
1.267](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb84a8e2c-e79f-4c5e-abb1-0c86f42e2c47%2F6bbb3bdb-3c3b-4e53-88ca-e82e7760728f%2Fs1t7b0u9_processed.jpeg&w=3840&q=75)
Transcribed Image Text:. Associate the diagnostic peaks in the IR with functional groups, and assign the
signals in the NMR to specific protons. Use this information to deduce the
structures of your compounds.
1.4
1.3
1.2
Figure 5. NMR spectrum (300 MHz) of ethyl (R)-3-hydroxybutanoate, with chiral shift
reagent added.
1.404
1.383
1.315
1.292
1.267
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