Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Chapter 13.7, Problem 13.5P

Following are two constitutional isomers with the molecular formula C4H8O2.

Chapter 13.7, Problem 13.5P, Following are two constitutional isomers with the molecular formula C4H8O2. (a) Predict the number

  1. (a) Predict the number of signals in the 1H-NMR spectrum of each isomer.
  2. (b) Predict the ratio of areas of the signals in each spectrum.
  3. (c) Show how you can distinguish between these isomers on the basis of chemical shift.
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(a) Draw all six isomers of formula C4H8 (including stereoisomers).(b) For each structure, show how many types of H would appear in the proton NMR spectrum.(c) For each structure, show how many types of C would appear in the 13C NMR spectrum.(d) If an unknown compound of formula C4H8 shows two types of H and three types of C, can you determine its structurefrom this information?
The 1H NMR spectrum of 1,2-dimethoxyethane (CH3OCH2CH2OCH3) recorded on a 300 MHz NMR spectrometer consists of signals at 1017 Hz and 1065 Hz downeld from TMS. (a) Calculate the chemical shift of each absorption. (b) At what frequency would each absorption occur if the spectrum were recorded on a 500 MHz NMR spectrometer?
(a) Draw all six isomers of formula C4H8 (including stereoisomers).(b) For each structure, show how many types of H would appear in the proton NMR spectrum.(c) For each structure, show how many types of C would appear in the 13C NMR spectrum.

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NMR Spectroscopy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=SBir5wUS3Bo;License: Standard YouTube License, CC-BY