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
Chemistry for Engineering Students
4th Edition
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
Publisher:Lawrence S. Brown, Tom Holme
Chapter9: Energy And Chemistry
Section: Chapter Questions
Problem 9.36PAE: 9.36 Define the term calibration.
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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
![TMS
3.0
2.0
1.0
0.0
4.0
8 (ppm)
7.0
6.0
5.0
absorption of energy](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa6b1b262-121e-49b8-ae92-e57361f6e763%2Fd30eecb9-1f2a-4015-8323-83ee88c83876%2F9lluaf_processed.jpeg&w=3840&q=75)
Transcribed Image Text:TMS
3.0
2.0
1.0
0.0
4.0
8 (ppm)
7.0
6.0
5.0
absorption of energy
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