FW m Transmittance % Solvent: CDC13 4830 4000 2.10 1000 3000 CsH₂O2 2008 1983 2000 Wavenumber 1500 cm-1 3.0 1.01 2.5 1000 1000 300 500 3.15 The number underneath each peak in 'H NMR spectrum represents relative integration value.

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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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The IR, and 1H NMR spectra of a compound with formula C5H6O2 are shown below.  Determine the structure of the compound.  You must fill all the parts to this question in the given spaces.

FAY
Solvent: CDC13
D
4830
4000
2.10
Solution of problem # 2:
Degree of unsaturation:
IR interpretation:
3000
3000
Peak A (4.25 ppm)
4,0
C5H602
POOR
1983
2000 Wavenumber 1500
cm 1
3.0
1.01
2.5
The number underneath each peak in 'H NMR spectrum represents relative integration value.
Peak B (2.90 ppm)
1000
1000
800
500
'H NMR interpretation (I want a picture of the fragment that you can determine from the shift and
splitting):
Structure of unknown compound
3.15
Peak C (1.35 ppm)
Transcribed Image Text:FAY Solvent: CDC13 D 4830 4000 2.10 Solution of problem # 2: Degree of unsaturation: IR interpretation: 3000 3000 Peak A (4.25 ppm) 4,0 C5H602 POOR 1983 2000 Wavenumber 1500 cm 1 3.0 1.01 2.5 The number underneath each peak in 'H NMR spectrum represents relative integration value. Peak B (2.90 ppm) 1000 1000 800 500 'H NMR interpretation (I want a picture of the fragment that you can determine from the shift and splitting): Structure of unknown compound 3.15 Peak C (1.35 ppm)
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Molecular formula C5H6O2

IR and NMR spectra

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