a) Transmittance, % b) 1 group. c) 100 50 0 4000 E m, 2H 6 C = C-H MW =70.09 g/mol Molecular Formula = 120 3000 |}={{ For the IR spectrum illustrated below, identify and label major peaks with the appropriate functional C-H Sp³ d, 4H H-C-X Tt O 100 Show your analysis here! 4 с H Y 0 Elemental analysis, %: C, 68.55; H, 8.63; O, 22.83 2 (4) +2-6-4:2 cy Heo 4 For the ¹H-NMR spectrum given below, label each peak with the appropriate proton(s). 2000 C=0 80 Wavenumber, cm-1 3 PPM Page 4 of 5 O B > 68.55/12 = 5.71/1.42 = 4 8.63/1 = 8.63/1.42 = 6 22.83/16 = 1.42 / 1.42= 1 For the ¹3C-NMR spectrum illustrated below, label each peak with the carbon atom(s). R-CEC-H 1500 PPM 60 IHD = 2 1000 40 2 20 Circle the final answer 2 d) First, propose three reasonable structures that match the spectra. Second, provide a detailed structure elucidation and draw the structure of the compound represented by molecular formula and spectra given. Show your analysis. Draw possible structures 500

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Hi, we took notes on how to find structures, but I still don't understand. Can you help me with the bottom part?

a)
Transmittance, %
b)
1
group.
c)
100
50
0
4000
E
m, 2H
6
C = C-H
MW =70.09 g/mol
Molecular Formula =
120
3000
|}={{
For the IR spectrum illustrated below, identify and label major peaks with the appropriate functional
C-H
Sp³
d, 4H
H-C-X
Tt O
100
Show your analysis here!
4
с
H
Y 0
Elemental analysis, %: C, 68.55; H, 8.63; O, 22.83 2 (4) +2-6-4:2
cy Heo
4
For the ¹H-NMR spectrum given below, label each peak with the appropriate proton(s).
2000
C=0
80
Wavenumber, cm-1
3
PPM
Page 4 of 5
O B >
68.55/12 = 5.71/1.42 = 4
8.63/1 = 8.63/1.42 = 6
22.83/16 = 1.42 / 1.42= 1
For the ¹3C-NMR spectrum illustrated below, label each peak with the carbon atom(s).
R-CEC-H
1500
PPM
60
IHD =
2
1000
40
2
20
Circle the final answer
2
d) First, propose three reasonable structures that match the spectra. Second, provide a detailed structure
elucidation and draw the structure of the compound represented by molecular formula and spectra given.
Show your analysis.
Draw possible structures
500
Transcribed Image Text:a) Transmittance, % b) 1 group. c) 100 50 0 4000 E m, 2H 6 C = C-H MW =70.09 g/mol Molecular Formula = 120 3000 |}={{ For the IR spectrum illustrated below, identify and label major peaks with the appropriate functional C-H Sp³ d, 4H H-C-X Tt O 100 Show your analysis here! 4 с H Y 0 Elemental analysis, %: C, 68.55; H, 8.63; O, 22.83 2 (4) +2-6-4:2 cy Heo 4 For the ¹H-NMR spectrum given below, label each peak with the appropriate proton(s). 2000 C=0 80 Wavenumber, cm-1 3 PPM Page 4 of 5 O B > 68.55/12 = 5.71/1.42 = 4 8.63/1 = 8.63/1.42 = 6 22.83/16 = 1.42 / 1.42= 1 For the ¹3C-NMR spectrum illustrated below, label each peak with the carbon atom(s). R-CEC-H 1500 PPM 60 IHD = 2 1000 40 2 20 Circle the final answer 2 d) First, propose three reasonable structures that match the spectra. Second, provide a detailed structure elucidation and draw the structure of the compound represented by molecular formula and spectra given. Show your analysis. Draw possible structures 500
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