NMR Spectroscopy Question Given the compound: C18H24O3 And the information of the Hydrogen and Carbon NMR...

NMR Spectroscopy Question

Given the compound: C₁₈H₂₄O₃

_{And the information of the Hydrogen and Carbon NMR
Spectroscopy}

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 and justify 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 unknown please show both and justify our choice.

This is all the given information.

Expert Solution

queen_honey_blossom answered 10 months ago

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