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Analysis of a sweet-smelling, neutral compound of carbon, hydrogen and oxygen produced the following results: %C = 54.5; %H = 9.1. 3. From its mass spectrum, the molecular ion had a mass/charge ratio of 88. Its infra-red spectrum showed a prominent peak at 1735 cm-. Figure 121 shows the NMR spectrum of the compound. Figure 121 absorption of energy

Analysis of a sweet-smelling, neutral compound of carbon, hydrogen and oxygen produced the following results: %C = 54.5; %H = 9.1. 3. From its mass spectrum, the molecular ion had a mass/charge ratio of 88. Its infra-red spectrum showed a prominent peak at 1735 cm-. Figure 121 shows the NMR spectrum of the compound. Figure 121 absorption of energy

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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Suggest a structural Formula for this compound.

Analysis of a sweet-smelling, neutral compound of carbon, hydrogen and oxygen produced the following results: %C = 54.5; %H = 9.1. From its mass spectrum, the molecular ion had a mass/charge ratio of 88. Its infra-red spectrum showed a prominent peak at 1735 cm-!. Figure 121 shows the NMR spectrum of the compound. Figure 121 TMS 7.0 3.0 4.0 8 (ppm) 6.0 5.0 2.0 1.0 0.0 3. absorption of energy
Transcribed Image Text:Analysis of a sweet-smelling, neutral compound of carbon, hydrogen and oxygen produced the following results: %C = 54.5; %H = 9.1. From its mass spectrum, the molecular ion had a mass/charge ratio of 88. Its infra-red spectrum showed a prominent peak at 1735 cm-!. Figure 121 shows the NMR spectrum of the compound. Figure 121 TMS 7.0 3.0 4.0 8 (ppm) 6.0 5.0 2.0 1.0 0.0 3. absorption of energy
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