Label the significant peaks in the IR and NMR spectra. When analyzing the signals in the 1H NMR, be sure to include all appropriate information. For example: 3H, singlet, 0 neighbors, and c (the letter referring to the corresponding unique type of hydrogens that were labeled in the structure). It is recommended to provide

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Chapter1: Chemical Foundations
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Label the significant peaks in the IR and NMR spectra. When analyzing the signals in the 1H NMR, be sure to include all appropriate information. For example: 3H, singlet, 0 neighbors, and c (the letter referring to the corresponding unique type of hydrogens that were labeled in the structure). It is recommended to provide more analysis for each signal than what is described above, when necessary, such as labeling any coupling constants if any are provided. For 13C NMR label each peak to the corresponding carbon in your suggested structure. Include calculating degrees of unsaturation.

Label the significant peaks in the IR and NMR spectra. When analyzing the signals in the 'H NMR, be sure to include
all appropriate information. For example: 3H, singlet, 0 neighbors, and c (the letter referring to the corresponding
unique type of hydrogens that were labeled in the structure). It is recommended to provide more analysis for each
signal than what is described above, when necessary, such as labeling any coupling constants if any are provided.
For 13C NMR label each peak to the corresponding carbon in your suggested structure. Show all work for full credit,
including calculating degrees of unsaturation.
The following IR and NMR spectra are of a compound with the molecular formula of C3H14O3. Draw the
correct structure.
1000
Copyright © 1994
AVENUBERS
3H
2H
3H
2H
2H
4.5
4.0
Proton NMA
3.5
1.5
1.0 PPM
3.0
2.5
2.0
200
160
140 PPM
10 PPM O
Carbon 13 NMA
1157. 44
1829. 19 –
Transcribed Image Text:Label the significant peaks in the IR and NMR spectra. When analyzing the signals in the 'H NMR, be sure to include all appropriate information. For example: 3H, singlet, 0 neighbors, and c (the letter referring to the corresponding unique type of hydrogens that were labeled in the structure). It is recommended to provide more analysis for each signal than what is described above, when necessary, such as labeling any coupling constants if any are provided. For 13C NMR label each peak to the corresponding carbon in your suggested structure. Show all work for full credit, including calculating degrees of unsaturation. The following IR and NMR spectra are of a compound with the molecular formula of C3H14O3. Draw the correct structure. 1000 Copyright © 1994 AVENUBERS 3H 2H 3H 2H 2H 4.5 4.0 Proton NMA 3.5 1.5 1.0 PPM 3.0 2.5 2.0 200 160 140 PPM 10 PPM O Carbon 13 NMA 1157. 44 1829. 19 –
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