do # 3 part ab & c: 3. (a) Analyze the 'H NMR data (from 53.0-7.0) and complete the following table for (D)-(-)-carvone. Assign the alkene signals. Use the labeling convention provided for full credit. HA H3C. HB H3 Hc Ho HF HE Ho chemical shift (8) multiplicity coupling integration assignment constant (b) Analyze the H NMR data (from 53.0-7.0) for the epoxycarvone product. Use the same labeling convention as above. chemical shift (8) multiplicity coupling constant integration assignment (c) Based on the NMR data, which alkene reacted? Or did both alkenes react?

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do # 3 part ab & c:
3. (a) Analyze the 'H NMR data (from 53.0-7.0) and complete the following table for (D)-(-)-carvone.
Assign the alkene signals. Use the labeling convention provided for full credit.
HA H3C.
HB
H3 Hc
Ho
HF
HE
Ho
chemical shift
(8)
multiplicity
coupling
integration
assignment
constant
(b) Analyze the H NMR data (from 53.0-7.0) for the epoxycarvone product. Use the same labeling
convention as above.
chemical shift
(8)
multiplicity
coupling
constant
integration
assignment
(c) Based on the NMR data, which alkene reacted? Or did both alkenes react?
Transcribed Image Text:do # 3 part ab & c: 3. (a) Analyze the 'H NMR data (from 53.0-7.0) and complete the following table for (D)-(-)-carvone. Assign the alkene signals. Use the labeling convention provided for full credit. HA H3C. HB H3 Hc Ho HF HE Ho chemical shift (8) multiplicity coupling integration assignment constant (b) Analyze the H NMR data (from 53.0-7.0) for the epoxycarvone product. Use the same labeling convention as above. chemical shift (8) multiplicity coupling constant integration assignment (c) Based on the NMR data, which alkene reacted? Or did both alkenes react?
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