The 'H NMR spectrum of 1,2-dimethoxyethane (CH;OCH,CH2OCH3) recorded on a 300 MHzNMR spectrometer consists of signals at 1017 Hz and 1065 Hz downfield from TMS. (a) Calculatethe chemical shift of each absorption. (b) At what frequency would each absorption occur if thespectrum were recorded on a 500 MHz NMR spectrometer?

Given: Compound = 1,2-dimrthoxyethane (CH3OCH2CH2OCH3) Frequency of spectrometer = 300 MHz Observed…

Answered: The 'H NMR spectrum of…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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The 1H NMR spectrum of methylbenzene (C6H5CH3) recorded on a 500 Mhz spectrometer consists of signals at chemical shifts of 2.21 parts per million and 7.10 ppm. calculate the frequency, downfield of TMS, of each absorption.
The 1H NMR spectrum of chloromethane recorded on a 300 Hz NMR spectrometer consists of signals at 444 Hz and 1071 Hz downfield from TMS. Calculate the chemical shift of each absorption. Give answer in parts per million.
When the 1î-NMR spectrum of acetone, CH3COCH3, is recorded on an instrument operating at 200 MHz, a single sharp resonance at 2.1î is seen. (a) How many hertz downfield from TMS does the acetone resonance correspond to? (b) If the 1î-NMR spectrum of acetone were recorded at 500 MHz, what would the position of the absorption be in î units? (c) How many hertz downfield from TMS does this 500 MHz resonance correspond to?
How could 1H NMR spectroscopy be used to distinguish betweencompounds X and Y?
The 1H NMR spectrum of 1,2-dimethoxyethane (CH3OCH32CH2OCH3) recorded on a 300 MHz NMR spectrometer consists of signals at 1017 Hz and 1065 Hz downfield 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?
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?
How would integration distinguish the 1H NMR spectra of the following compounds?
A signal is seen at 600 Hz from the TMS signal in an NMR spectrometer with a 300-MHz operating frequency. a. What is the chemical shift of the signal? b. What is its chemical shift in an instrument operating at 500 MHz? c. How many hertz from the TMS signal is the signal in a 500-MHz spectrometer?
Calculate the HDI of each FM and propose 2structures for two molecules that are isomers.Specify what the indicated absorption (s) shouldbe to.a.C7H15NO with strong absorptions in 3400, 3270and 1670, 1390, and 1370 cm-1b. C6H10O with absorptions in 2065 (m), 1685 (f),1650 (m) and 970 (f) cm-1c. C9H12O, with absorptions in 1600 and 1500 and1245 cm-1.
Describe the 1H NMR spectrum of each compound. State how many NMR signals are present, the splitting pattern for each signal, and the approximate chemical shift
Explain the appearance of the 1H-NMR spectrum of 1,1,2-trichloroethane. How many signals would you expect, and into how many peaks will each of the signals be split?
When 2-bromo-3,3-dimethylbutane is treated with K+ −OC(CH3)3, a single product T having molecular formula C6H12 is formed. When 3,3dimethylbutan-2-ol is treated with H2SO4, the major product U has the same molecular formula. Given the following 1H NMR data, what are the structures of T and U? Explain in detail the splitting patterns observed for the three split signals in T. 1H NMR of T: 1.01 (singlet, 9 H), 4.82 (doublet of doublets, 1 H, J = 10, 1.7 Hz), 4.93 (doublet of doublets, 1 H, J = 18, 1.7 Hz), and 5.83 (doublet of doublets, 1 H, J = 18, 10 Hz) ppm 1H NMR of U: 1.60 (singlet) ppm

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