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. Suggest a structural Formula for 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. Suggest a structural Formula for 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. Suggest a structural Formula for this compound.
- A) 3-hydroxybutanal
- B) Methyl propionate
- C) Ethyl acetate
- D) 2-methylpropanoic acid
- E) Methoxyacetone
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