Hydroboration-oxidation of an alkene,
C7H12, gives a single product that exhibits
13C spectral data below.
Broadband-decoupled 13C NMR: 26.1, 26.9,
29.9, 40.5, 68.2 δ
DEPT-90: 40.5 δ
DEPT-135: positive peaks at 40.5; negative peaks at
26.1, 26.9, 29.9, 68.2 δ
Draw a structure for this compound.
You do not have to consider stereochemistry.
You do not have to explicitly draw H atoms.
In cases where there is more than one answer, just draw one.