Organic Chemistry
Organic Chemistry
6th Edition
ISBN: 9781936221349
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Chapter 14, Problem 14.4P
Interpretation Introduction

Interpretation:

The compound with a molecular mass of 82 and given spectroscopic data is to be identified.

Concept introduction:

Spectroscopy method is used to identify the structure of the molecule. It is based on the interactions between matter and electromagnetic radiations. Proton NMR spectroscopy identifies the number of hydrogen atoms present in a molecule and the nature of the functional group. The value of chemical peaks depends upon the chemical environment around the hydrogen atom.

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A compound with the molecular formula C11H14O2 has a strong IR peak at 1740 cm-1 and the 1H NMR is shown. a) Determine the elements of unsaturation. b) What functional group is indicated by the IR? c) Draw out the structure of the compound.
What is the structure of the compound with the formula C10H10O4, if it shows strong IR signal near 3050 and 1730 cm-1, the 1H-NMR spectrum shows only two signals, both singlets. One of them appears at 3.9 ppm with the relative integration value of 79 and the second one appears at 8.1 ppm with the relative integration of 52.
what is is the structure of a compound of molecular formula c 10 h 14 o 2 that shows a strong ir absorption at 3150-2850 cm − 1 and give the following 1 h nmr absorptions: 1.4 (triplet, 6 h), 4.0 (quarter, 4h), and 6.8 (singlet, 4h) ppm?
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NMR Spectroscopy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=SBir5wUS3Bo;License: Standard YouTube License, CC-BY