NMR Spectroscopy Question
Given the compound:C18H24O3
And the information of the Hydrogen and Carbon NMRSpectroscopy
1H: 10.1, doublet, 1; 7.2, singlet, 1; 2.4, quartet,1; 1.5, quint, 2; 1.2, t, 3
13C: 199, 130, 125, 31, 23, 20
1. Calculate degree on unsaturation
2. Draw 1H and 13C NMRs. Assign a fragment to each peak andjustify your choice using tools such as the N+1 rule
3. Draw a structure of your unknown
4. If there is more than one structure possible for your unknownplease show both and justify our choice.
This is all the given information.
