Mass Spectrum (not shown): [M] 191 (100%) m/z Infrared Spectrum (not shown): 3323, 3025, 3000, 2249 (m), 1603, 1520 cm³ (all listed are strong (s) unless otherwise indicated) ¹H Nuclear Magnetic Resonance dd (J = 8,2 Hz) d (J= 2 Hz) (J= 8 Hz) -50 PPM 2H 24 (C) (CH) 7 1H 1H 1H 1H 13C Nuclear Magnetic Resonance 3x (CH) & (C) (C) (C) 3 24 2H 2 3H 2H (CH2) (CH2) (CH3) 140 120 100 80 60 40 20 PPM

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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Given the attached data, provide the drawing for the corresponding structure. 

Mass Spectrum (not shown): [M] 191 (100%) m/z
Infrared Spectrum (not shown): 3323, 3025, 3000, 2249 (m), 1603, 1520 cm³ (all listed are strong (s) unless
otherwise indicated)
¹H Nuclear Magnetic Resonance
dd
(J = 8,2 Hz)
d
(J= 2 Hz)
(J= 8 Hz)
-50
PPM
2H
24
(C)
(CH)
7
1H 1H 1H
1H
13C Nuclear Magnetic Resonance
3x (CH) & (C)
(C) (C)
3
24
2H
2
3H
2H
(CH2) (CH2)
(CH3)
140
120
100
80
60
40
20
PPM
Transcribed Image Text:Mass Spectrum (not shown): [M] 191 (100%) m/z Infrared Spectrum (not shown): 3323, 3025, 3000, 2249 (m), 1603, 1520 cm³ (all listed are strong (s) unless otherwise indicated) ¹H Nuclear Magnetic Resonance dd (J = 8,2 Hz) d (J= 2 Hz) (J= 8 Hz) -50 PPM 2H 24 (C) (CH) 7 1H 1H 1H 1H 13C Nuclear Magnetic Resonance 3x (CH) & (C) (C) (C) 3 24 2H 2 3H 2H (CH2) (CH2) (CH3) 140 120 100 80 60 40 20 PPM
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