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Hydroboration-oxidation of an alkene, C7H12, gives a single product that exhibits 13C spectral data below. Broadband-decoupled...

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.

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queen_honey_blossom answered 2 years ago
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