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The NMR spectra for compound 1 were acquired in a 10 mg / 0.6 mL solution of CDCl3. The 1H and 13C peaks are also listed below. Provide a full analysis of the NMR spectra for compound 1. 1H NMR (400 MHz, CDCl3) δ 5.94 (dd, J = 17.3, 10.8 Hz, 1H), 5.24 (dd, J = 17.4, 1.2 Hz, 1H), 5.14 (tt, J = 7.1, 1.5 Hz, 1H), 5.08 (dd, J = 10.8, 1.3 Hz, 1H), 2.05 (p, J = 7.3 Hz, 2H), 1.70 (s, 3H), 1.63 (s, 3H), 1.60 – 1.57 (m, 2H), 1.30 (s, 3H). 13C NMR (100 MHz, CDCl3) δ 145.05, 131.98, 124.32, 111.69, 73.49, 42.06, 27.89, 25.71, 22.81, 17.70. Note: from the data given, the two terminal methyl groups are impossible to differentia

The NMR spectra for compound 1 were acquired in a 10 mg / 0.6 mL solution of CDCl3. The 1H and 13C peaks are also listed below. Provide a full analysis of the NMR spectra for compound 1. 1H NMR (400 MHz, CDCl3) δ 5.94 (dd, J = 17.3, 10.8 Hz, 1H), 5.24 (dd, J = 17.4, 1.2 Hz, 1H), 5.14 (tt, J = 7.1, 1.5 Hz, 1H), 5.08 (dd, J = 10.8, 1.3 Hz, 1H), 2.05 (p, J = 7.3 Hz, 2H), 1.70 (s, 3H), 1.63 (s, 3H), 1.60 – 1.57 (m, 2H), 1.30 (s, 3H). 13C NMR (100 MHz, CDCl3) δ 145.05, 131.98, 124.32, 111.69, 73.49, 42.06, 27.89, 25.71, 22.81, 17.70. Note: from the data given, the two terminal methyl groups are impossible to differentia

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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The NMR spectra for compound 1 were acquired in a 10 mg / 0.6 mL solution of CDCl3. The 1H and 13C peaks are also listed below.
Provide a full analysis of the NMR spectra for compound 1.

1H NMR (400 MHz, CDCl3) δ 5.94 (dd, J = 17.3, 10.8 Hz, 1H), 5.24 (dd, J = 17.4, 1.2 Hz,
1H), 5.14 (tt, J = 7.1, 1.5 Hz, 1H), 5.08 (dd, J = 10.8, 1.3 Hz, 1H), 2.05 (p, J = 7.3 Hz, 2H),
1.70 (s, 3H), 1.63 (s, 3H), 1.60 – 1.57 (m, 2H), 1.30 (s, 3H).
13C NMR (100 MHz, CDCl3) δ 145.05, 131.98, 124.32, 111.69, 73.49, 42.06, 27.89, 25.71,
22.81, 17.70.
Note: from the data given, the two terminal methyl groups are impossible to differentia

НО 1
Transcribed Image Text:НО 1
| A (dd) | 5.94 0.99- کر کر کر بر 6.00 5.95 5.90 5.85 B (dd) 5.24 C (tt) | D (dd) 5.14 5.08 |||| || !! th Mh E (p) 2.05 | H (m) 1.59 F(s) Gs) | 1,70 1,63 1-50 € Its) 1.30 5.25 5.20 5.15 5.10 5.05 2.10 2.05 2.00 1.95 1.90 1.85 1.80 1.75 1.70 1.65 1.60 1.55 1.50 1.45 1.40 1.35 1.30 1.25 f1 (ppm) -22000 --21000 -20000 -19000 -18000 -17000 -16000 15000 -14000 13000 -12000 -11000 -10000 -9000 -8000 -7000 -6000 -5000 --4000 -3000 -2000 -1000 -0 -1000 --2000
Transcribed Image Text:| A (dd) | 5.94 0.99- کر کر کر بر 6.00 5.95 5.90 5.85 B (dd) 5.24 C (tt) | D (dd) 5.14 5.08 |||| || !! th Mh E (p) 2.05 | H (m) 1.59 F(s) Gs) | 1,70 1,63 1-50 € Its) 1.30 5.25 5.20 5.15 5.10 5.05 2.10 2.05 2.00 1.95 1.90 1.85 1.80 1.75 1.70 1.65 1.60 1.55 1.50 1.45 1.40 1.35 1.30 1.25 f1 (ppm) -22000 --21000 -20000 -19000 -18000 -17000 -16000 15000 -14000 13000 -12000 -11000 -10000 -9000 -8000 -7000 -6000 -5000 --4000 -3000 -2000 -1000 -0 -1000 --2000
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