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Molecular Formula:C6H1202, EOU = IR (cm-1): 2951 bond 1743 bond Fill-up this > M+ (m/z) 1H NMR (ppm): amu 1.056 ppm, triplet (3H), J = 7.2 Hz 1.449 ppm, doublet (6H), J =7.0 Hz 2.278 ppm, quartet (2H), J =7.2 Hz 4.815 ppm, septet (1 H), J = 7.0 Hz 8 (ppm) 13C NMR (ppm): 21.9 ppm, (2C) 9.5 ppm (1C) 27.8 ppm (1C) 68.8 ppm (1 C) 174 ppm (1 C) 50 100 150 8 foomi Structure (Match the data with each group with multiplicity) 'H NMR 13C NMR

Molecular Formula:C6H1202, EOU = IR (cm-1): 2951 bond 1743 bond Fill-up this > M+ (m/z) 1H NMR (ppm): amu 1.056 ppm, triplet (3H), J = 7.2 Hz 1.449 ppm, doublet (6H), J =7.0 Hz 2.278 ppm, quartet (2H), J =7.2 Hz 4.815 ppm, septet (1 H), J = 7.0 Hz 8 (ppm) 13C NMR (ppm): 21.9 ppm, (2C) 9.5 ppm (1C) 27.8 ppm (1C) 68.8 ppm (1 C) 174 ppm (1 C) 50 100 150 8 foomi Structure (Match the data with each group with multiplicity) 'H NMR 13C NMR

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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Obtain the structure of organic compound that is consistent with the spectroscopic data (see also spectra) given below . Show all NMR data on each and every group in the structure. [full characterization needed ]
Molecular Formula:C6H1202, EOU = IR (cm-1): 2951 bond 1743 bond Fill-up this → M+ (m/z) 1H NMR (ppm): amu 1.056 ppm, triplet (3H), J = 7.2 Hz 1.449 ppm, doublet (6H), J =7.0 Hz 2.278 ppm, quartet (2H), J =7.2 Hz 4.815 ppm, septet (1 H), J = 7.0 Hz 8 (ppm) 13C NMR (ppm): 21.9 ppm, (2C) 9.5 ppm (1C) 27.8 ppm (1C) 68.8 ppm (1 C) 174 ppm (1 C) 50 100 150 8 (oom) Structure (Match the data with each group with multiplicity) 'H NMR 13C NMR
Transcribed Image Text:Molecular Formula:C6H1202, EOU = IR (cm-1): 2951 bond 1743 bond Fill-up this → M+ (m/z) 1H NMR (ppm): amu 1.056 ppm, triplet (3H), J = 7.2 Hz 1.449 ppm, doublet (6H), J =7.0 Hz 2.278 ppm, quartet (2H), J =7.2 Hz 4.815 ppm, septet (1 H), J = 7.0 Hz 8 (ppm) 13C NMR (ppm): 21.9 ppm, (2C) 9.5 ppm (1C) 27.8 ppm (1C) 68.8 ppm (1 C) 174 ppm (1 C) 50 100 150 8 (oom) Structure (Match the data with each group with multiplicity) 'H NMR 13C NMR
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