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inessss [21]
3 years ago
14

Draw a structure for a compound that meets the following description: An optically active compound, C5H10O with an IR absorption

at 1730 cm-1.

Chemistry
1 answer:
Elenna [48]3 years ago
5 0

Question: A optically active compound, C5H10O, exhibits IR absorption at 1730 cm-1.

Its carbon NMR shifts are given below. The number of hydrogen's at each carbon, determined by DEPT, is given in parentheses after the chemical shift.

13C NMR: δ 22.6 (3), 23.6 (1), 52.8 (2), 202.4 (1)

Draw the structure of this compound in the window below

Explanation:

3-methylbutanal is a butanal substituted by the methyl group at the 3rd position. It is a volatile constituent in the olive. Also, it is used as a flavoring agent and a plant metabolite, it is also a Saccharomyces cerevisiae metabolite. It is also called as the Isovaleraldehyde organic compound. The liquid is colorless at STP, and also found in very low concentrations. It is also seen to be produced commercially for different use. Mostly used compound reagent in the preparation of pharmaceuticals and pesticides.

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Answer:

See explanation

Explanation:

All molecules possess the London dispersion forces. However London dispersion forces is the only kind of intermolecular interaction that exists in nonpolar substances.

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As for ethyl alcohol, the molecule is polar due to the presence of polar O-H bond. In addition to London dispersion forces, dipole-dipole interactions and specifically hydrogen bonding also occurs between the molecules.

Because ethyl alcohol is polar, it is more soluble in water than dimethyl ether.

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