Determine the structure: A compound has an M+ peak of 104. Its proton NMR shows the following: 1.3 ppm 3H triplet 3.6 ppm 2H quartet 4.1 ppm 2H singlet 10.2 ppm 1H singlet, disappears when solvent is D₂O. The IR:

Determine the structure: A compound has an M+ peak of 104. Its proton NMR shows the following: 1.3 ppm 3H triplet 3.6 ppm 2H quartet 4.1 ppm 2H singlet 10.2 ppm 1H singlet, disappears when solvent is D₂O. The IR:

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

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.30P

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Concept explainers

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

LCD
M
3000
TRANSMITTANCEIXI
4100
2000
HAVENUMBER
1500
1000
حسن
510

Determine the structure:
A compound has an M+ peak of 104.
Its proton NMR shows the following:
1.3 ppm 3H triplet
3.6 ppm 2H quartet
4.1 ppm 2H singlet
10.2 ppm 1H singlet, disappears when solvent is D₂O.
The IR:

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