Identify the structure of the compound a with a formula of C 3 H 6 O 2 having the following IR, and 1 H NMR spectra (integrals and multiplicity shown in the boxes: s-singlet, d-doublet, t-triplet, q-quartet, etc

Identify the structure of the compound a with a formula of C 3 H 6 O 2 having the following IR, and 1 H NMR spectra (integrals and multiplicity shown in the boxes: s-singlet, d-doublet, t-triplet, q-quartet, etc.). Label the spectra with proper information you deduced (functional groups, number of protons, fragments, etc.). Compound formula. C 3 H 6 O 2 Questions to you decide What is the element of unsaturation of the molecular formula? Show the equation you use: What are the functional groups present in this molecule? Show all of them belowDraw at least two possible structures that have the . required element of unsaturation as well as the observed functional groups: Based on the 1 H NMR above, what molecular fragmentations do you see: Draw your final decision of the structure below. Is this one of the structures in your answer 5C? Transcribed Image Text: Compound formula. C3H6O2
L00
IR
4000
5000
2000
1500
1000
MAVENUMB ERI l Transcribed Image Text: 3H, t
ΙΗ ΝMR
2H, q
1H,broad
Disappears when 1 drop of D20 was added.
12
11
10
8.
5
4
3

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