Mass Spectrum (not shown): [M] = 298 (100%) m/z Infrared Spectrum (not shown): 3098, 3023, 2940, 1750, 1702, 1590, 1497 cm¹ (all listed are strong (s) unless otherwise indicated) ¹H Nuclear Magnetic Resonance 9 8 d(J=8 Hz) d(J-8 Hz) t (obscured) t(J=2Hz) dt (J 8,2 Hz) (J-8 Hz) dt (J-8,2 Hz) 8 7 q 7 6 5 PPM 2H 2H 2H2H 1H1H 1H1H 13C Nuclear Magnetic Resonance (CH) || (CH) -2 0 3H 3H 3x (C) 3x (CH) (C) (C) (C) | (CH) (CH2) (CH2) (CH3) (CH3) 180 160 140 120 100 PPM 80 60 60 40 40 20 20

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter14: Mass Spectrometry
Section: Chapter Questions
Problem 14.26P: Following is the mass spectrum of bromocyclopentane. The molecular ion m/z 148 is of such low...
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Provide the drawing of the unknown structure that corresponds with this data. 

Mass Spectrum (not shown): [M] = 298 (100%) m/z
Infrared Spectrum (not shown): 3098, 3023, 2940, 1750, 1702, 1590, 1497 cm¹ (all listed are strong (s) unless
otherwise indicated)
¹H Nuclear Magnetic Resonance
9
8
d(J=8 Hz)
d(J-8 Hz)
t
(obscured)
t(J=2Hz)
dt (J 8,2 Hz)
(J-8 Hz)
dt (J-8,2 Hz)
8
7
q
7
6
5
PPM
2H
2H
2H2H 1H1H 1H1H
13C Nuclear Magnetic Resonance
(CH) || (CH)
-2
0
3H 3H
3x (C)
3x (CH)
(C) (C)
(C) | (CH)
(CH2)
(CH2) (CH3) (CH3)
180
160
140
120
100
PPM
80
60
60
40
40
20
20
Transcribed Image Text:Mass Spectrum (not shown): [M] = 298 (100%) m/z Infrared Spectrum (not shown): 3098, 3023, 2940, 1750, 1702, 1590, 1497 cm¹ (all listed are strong (s) unless otherwise indicated) ¹H Nuclear Magnetic Resonance 9 8 d(J=8 Hz) d(J-8 Hz) t (obscured) t(J=2Hz) dt (J 8,2 Hz) (J-8 Hz) dt (J-8,2 Hz) 8 7 q 7 6 5 PPM 2H 2H 2H2H 1H1H 1H1H 13C Nuclear Magnetic Resonance (CH) || (CH) -2 0 3H 3H 3x (C) 3x (CH) (C) (C) (C) | (CH) (CH2) (CH2) (CH3) (CH3) 180 160 140 120 100 PPM 80 60 60 40 40 20 20
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