From the given values of ¹H-NMR data, predict the structure of the organic compound with the molecular formula C₁4H₁0O -8.5 ppm (d), 7.5 ppm (m), 7.4 ppm (m), 7.25 ppm (d), 4.30 ppm (s)Also, assign the peaks in the structure deduced.

Firstly we find the double bond equivalent of the compound. And then we figure out the presence of…

From the given values of ¹H-NMR data, predict the structure of the organic compound with the molecular formula C₁4H10O - 8.5 ppm (d), 7.5 ppm (m), 7.4 ppm (m), 7.25 ppm (d), 4.30 ppm (s) Also, assign the peaks in the structure deduced.

From the given values of ¹H-NMR data, predict the structure of the organic compound with the molecular formula C₁4H10O - 8.5 ppm (d), 7.5 ppm (m), 7.4 ppm (m), 7.25 ppm (d), 4.30 ppm (s) Also, assign the peaks in the structure deduced.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter23: Amines

Section: Chapter Questions

Problem 23.39P

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Analyzing and Predicting Spectroscopic Data

The interaction of electromagnetic radiation with the structure of molecules in the sample and their study is referred spectroscopy. Several spectroscopic methods are used to acquire sample information, and these methods are proved to be accurate, fast, and non-destructive. The information obtained about the content and composition of molecules from these spectroscopic methods is called spectroscopic data.

Question

From the given values of ¹H-NMR data, predict the structure of the organic compound with the molecular formula C₁4H₁0O -
8.5 ppm (d), 7.5 ppm (m), 7.4 ppm (m), 7.25 ppm (d), 4.30 ppm (s)
Also, assign the peaks in the structure deduced.

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