The three compounds shown below are structural isomers of each other. Matcheach compound with its corresponding mass spectrum and draw the fragment ioncorresponding to the base peak in each.а.b.ОНH100Compound8060Fragment4020 -1020304050607080m/z100Compound80 -60Fragment40 -201020304050607080m/z100 -CompoundMS-NW-06618060Fragment4020102030405060708090100m/zRelative IntensityRelative IntensityRelative Intensity

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The three compounds shown below are structural isomers of each other. Ma each compound with its corresponding mass spectrum and draw the fragment corresponding to the base peak in each. а. b. с. НО H' 100 - Compound 80 60 Fragment 40 20 omtt tr mm 10 20 30 40 50 60 70 80 m/z 100 Compound 80 60 Fragment 40 20 10 20 30 40 50 60 70 80 m/z 100 Compound MS-NU-0661 80 60 Fragment 40 Relative Intensity Relative Intensity Relative Intensity

The three compounds shown below are structural isomers of each other. Ma each compound with its corresponding mass spectrum and draw the fragment corresponding to the base peak in each. а. b. с. НО H' 100 - Compound 80 60 Fragment 40 20 omtt tr mm 10 20 30 40 50 60 70 80 m/z 100 Compound 80 60 Fragment 40 20 10 20 30 40 50 60 70 80 m/z 100 Compound MS-NU-0661 80 60 Fragment 40 Relative Intensity Relative Intensity Relative Intensity

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy

Section12.SE: Something Extra

Problem 20AP: The hormone cortisone contains C, H, and O, and shows a molecular ion at M+=360.1937 by...

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