Construct a simulated 1H NMR spectrum for wet ethanol, CH3CH2OH. Assume that the hydroxyl proton is not coupled with any other protons. Drag the appropriate splitting patterns to the approximate chemical shift positions. Splitting patterns may be used more than once, or not at all, as needed. Likewise, some chemical shift bins might remain blank. Note that peak heights are arbitrary and do not indicate proton integrations. We are given that the hydroxyl proton is not coupled with any other protons. Therefore, its resonance will appear as a singlet. Keep in mind that electronegative groups move chemical shifts downfield (i.e., to higher ppm values). The hydroxyl proton is attached to an electronegative atom and will be strongly shifted downfield.