A compound gives a mass spectrum with peaks at mize 77 (40%), 112 (100%), 114 (33%), and essentially no other peaks E Deduce the molecular formula of the compound and the IHD (show the workout of the caloulations in detail) Il. Draw the chemical structure of the compound CH, CH, CH, Hu > C C,H. up C,H, CH, C,H C,H, 127

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 14.27P: Following is the mass spectrum of an unknown compound. The two highest peaks are at m/z 120 and 122....
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A compound gives a mass spectrum with peaks at mize 77 (40%), 112 (100%), 114 (33%), and essentially no other peaks
E Deduce the molecular formula of the compound and the IHD (show the workout of the caloulations in detail)
Il. Draw the chemical structure of the compound
CH,
CH,
CH,
Hu > C
C,H.
sip
C,H,
CH,
CH,
127
CH,
Transcribed Image Text:A compound gives a mass spectrum with peaks at mize 77 (40%), 112 (100%), 114 (33%), and essentially no other peaks E Deduce the molecular formula of the compound and the IHD (show the workout of the caloulations in detail) Il. Draw the chemical structure of the compound CH, CH, CH, Hu > C C,H. sip C,H, CH, CH, 127 CH,
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