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Use the following spectroscopic data to work out the structure of an organic compound: IR Spectrum 4000 (quid film) 100 80 60 40 20 % of base peak 1715 3000 2000 1600 1200 800 V (cm³) M+ 74 Mass Spectrum 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH₂ CH₂t CHt proton decoupled solvent No significant UV absorption above 220 nm 1 200 160 120 80 40 ° 5 (ppm) 1H NMR Spectrum (200 MHz, CDCI, solution) exchanges with D₂O T L 12 11 10 9 8 7 6 5 4 3 2 1 TMS L 8 (ppm)

Use the following spectroscopic data to work out the structure of an organic compound: IR Spectrum 4000 (quid film) 100 80 60 40 20 % of base peak 1715 3000 2000 1600 1200 800 V (cm³) M+ 74 Mass Spectrum 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH₂ CH₂t CHt proton decoupled solvent No significant UV absorption above 220 nm 1 200 160 120 80 40 ° 5 (ppm) 1H NMR Spectrum (200 MHz, CDCI, solution) exchanges with D₂O T L 12 11 10 9 8 7 6 5 4 3 2 1 TMS L 8 (ppm)

Chemistry
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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Use the following spectroscopic data to work out the structure of an organic compound: IR Spectrum 4000 (quid film) 100 80 60 40 20 % of base peak 1715 3000 2000 1600 1200 800 V (cm³) M+ 74 Mass Spectrum 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH₂ CH₂t CHt proton decoupled solvent No significant UV absorption above 220 nm 1 200 160 120 80 40 ° 5 (ppm) 1H NMR Spectrum (200 MHz, CDCI, solution) exchanges with D₂O T L 12 11 10 9 8 7 6 5 4 3 2 1 TMS L 8 (ppm)
Transcribed Image Text:Use the following spectroscopic data to work out the structure of an organic compound: IR Spectrum 4000 (quid film) 100 80 60 40 20 % of base peak 1715 3000 2000 1600 1200 800 V (cm³) M+ 74 Mass Spectrum 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH₂ CH₂t CHt proton decoupled solvent No significant UV absorption above 220 nm 1 200 160 120 80 40 ° 5 (ppm) 1H NMR Spectrum (200 MHz, CDCI, solution) exchanges with D₂O T L 12 11 10 9 8 7 6 5 4 3 2 1 TMS L 8 (ppm)
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