Problem # 2 Determine the structure of the compound with the spectra provided and molecular formula C5H₁00. I 200 180 10 9 8 160 140 7 120 6 1100 5 100 80 4 60 3 2000 3H singlet 6H doublet 37 1H septet 40 20 2 1 0 0

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Problem # 2 Determine the structure of the compound with the spectra provided and molecular
formula C5H100.
I
200 180 160
T
10
9
8
2000
140 120
1100
7 6 5
100
80
4
60
1000
3H singlet
6H doublet
37
1H septet
3 2
за
40 20 0
1
500
0
Transcribed Image Text:Problem # 2 Determine the structure of the compound with the spectra provided and molecular formula C5H100. I 200 180 160 T 10 9 8 2000 140 120 1100 7 6 5 100 80 4 60 1000 3H singlet 6H doublet 37 1H septet 3 2 за 40 20 0 1 500 0
Expert Solution
Step 1: Given

The molecular formula is C5H10O.

The FTIR, 1H, and 13C NMR spectra of the compound are given.

We have to determine the molecular structure of the compound.

The double bond equivalency (DBE) of that compound is

DBE = (No. of carbon atoms + 1) - {(No. of monovalent atoms - No. of trivalent atoms)/2} = (5+1)-(10/2) = 6-5 = 1.

So, the given compound has one degree of unsaturation.

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