A compound of formula C11H16N2 gives the IR, 1H NMR, and 13C NMR spectra shown. The proton NMR peak at δ 2 disappears on shaking with D2 Propose a structure for this compound, and show how your structure accounts for the observed absorptions. 2.51008060402004000STRANSMITTANCE200103500318093.5300016084250014074.5wavelength (um)5.5 652000 1800 1600 1400wavenumber (cm-¹)12010080(CH)||(CH)(CH)658 (ppm)8 9 101200 100060(CH₂)(CH₂)2311 1240d(CH₂)28002013114 15 1600600

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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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A compound of formula C11H16N2 gives the IR, 1H NMR, and 13C NMR spectra shown. The proton NMR peak at δ 2 disappears on shaking with D2 Propose a structure for this compound, and show how your structure accounts for the observed absorptions.

2.5
100
80
60
40
20
0
4000
STRANSMITTANCE
200
10
3500
3
180
9
3.5
3000
160
8
4
2500
140
7
4.5
wavelength (um)
5.5 6
5
2000 1800 1600 1400
wavenumber (cm-¹)
120
100
80
(CH)||(CH)
(CH)
6
5
8 (ppm)
8 9 10
1200 1000
60
(CH₂)
(CH₂)
2
3
11 12
40
d
(CH₂)
2
800
20
13
1
14 15 16
0
0
600

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