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–1. Figure below shows the NMR spectrum of the compound. Which of the following is this compound? A. 3-hydroxybutanal B. Methyl propionate C. Ethyl acetate D. 2-methylpropanoic acid E. Methoxyacetone
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–1. Figure below shows the NMR spectrum of the compound. Which of the following is this compound? A. 3-hydroxybutanal B. Methyl propionate C. Ethyl acetate D. 2-methylpropanoic acid E. Methoxyacetone
Physical Chemistry
2nd Edition
ISBN:9781133958437
Author:Ball, David W. (david Warren), BAER, Tomas
Publisher:Ball, David W. (david Warren), BAER, Tomas
Chapter20: Kinetics
Section: Chapter Questions
Problem 20.80E
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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. 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–1. Figure below shows the NMR spectrum of the compound. Which of the following is this compound?
A. 3-hydroxybutanal
B. Methyl propionate
C. Ethyl acetate
D. 2-methylpropanoic acid
E. Methoxyacetone
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