13. Draw the structure of the compound described below Hydroboration-oxidation of an alkene, C,H12, gives a single product that exhibits 13C spectral data below. Broadband-decoupled 1°C NMR: 26.1, 26.9, 29.9, 40.5, 68.2 8 DEPT-90: 40.5 8 DEPT-135: positive peaks at 40.5; negative peaks at 26.1, 26.9, 29.9, 68.2 8

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Draw the structure of the compund described below:

13. Draw the structure of the compound described below
Hydroboration-oxidation of an alkene, C,H12, gives a single product that exhibits 13C spectral
data below.
Broadband-decoupled 1C NMR: 26.1, 26.9, 29.9, 40.5, 68.2 8
DEPT-90: 40.5 8
DEPT-135: positive peaks at 40.5; negative peaks at 26.1, 26.9, 29.9, 68.2 8
Transcribed Image Text:13. Draw the structure of the compound described below Hydroboration-oxidation of an alkene, C,H12, gives a single product that exhibits 13C spectral data below. Broadband-decoupled 1C NMR: 26.1, 26.9, 29.9, 40.5, 68.2 8 DEPT-90: 40.5 8 DEPT-135: positive peaks at 40.5; negative peaks at 26.1, 26.9, 29.9, 68.2 8
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