The 'H NMR spectrum of 1-nitronaphthalene recorded at 298K in CDC!3 solution is given below. The 2-dimensional 'H NOESY spectrum is given on the facing page. Given that the nitro group at position 1 will always extensively deshield the proton at position 8 such that it will appear as the resonance at lowest field in the spectrum, use the NOESY spectrum to assign all of the other protons in the spectrum. Hg NO2 1-nitronaphthalene H7. H3 H5 H4 'H NMR Spectrum (400 MHz, CDCI, sołution) solvent residual 8.8 8.6 8.4 8.2 8.0 7.8 7.6 7.4 7.2 ppm Proton Chemical Shift (8) in ppm H2 H3 H4 H5 H6 H7 H8 8.56

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy
Section13.SE: Something Extra
Problem 56GP: Long-range coupling between protons more than two carbon atoms apart is sometimes observed when ...
icon
Related questions
Question

SHow solution

'H NOESY spectrum of 1-nitronaphthalene (recorded in CDC13 solution at 298K at
400 MHz).
H3 NO2
H7.
`H3
H5 H4
ppm
'H-'H NOESY Spectrum
(400 MHz; CDCI, solution)
7.4
7.6
7.8
8.0
8.2
8.4
8.6
8.6
8.4
8.2
8.0
7.8
7.6
7.4
ppm
Transcribed Image Text:'H NOESY spectrum of 1-nitronaphthalene (recorded in CDC13 solution at 298K at 400 MHz). H3 NO2 H7. `H3 H5 H4 ppm 'H-'H NOESY Spectrum (400 MHz; CDCI, solution) 7.4 7.6 7.8 8.0 8.2 8.4 8.6 8.6 8.4 8.2 8.0 7.8 7.6 7.4 ppm
The 'H NMR spectrum of 1-nitronaphthalene recorded at 298K in CDCI3 solution is
given below. The 2-dimensional 'H NOESY spectrum is given on the facing page.
Given that the nitro group at position 1 will always extensively deshield the proton at
position 8 such that it will appear as the resonance at lowest field in the spectrum, use
the NOESY spectrum to assign all of the other protons in the spectrum.
Hg NO2
1-nitronaphthalene
H7.
H6
H3
H5 H4
1H NMR Spectrum
(400 MHz, CDCI, solution)
solvent
residual
8.8
8.6
8.4
8.2
8.0
7.8
7.6
7.4
7.2
ppm
Proton
Chemical Shift (8) in ppm
H2
H3
Н4
H5
H6
H7
H8
8.56
Transcribed Image Text:The 'H NMR spectrum of 1-nitronaphthalene recorded at 298K in CDCI3 solution is given below. The 2-dimensional 'H NOESY spectrum is given on the facing page. Given that the nitro group at position 1 will always extensively deshield the proton at position 8 such that it will appear as the resonance at lowest field in the spectrum, use the NOESY spectrum to assign all of the other protons in the spectrum. Hg NO2 1-nitronaphthalene H7. H6 H3 H5 H4 1H NMR Spectrum (400 MHz, CDCI, solution) solvent residual 8.8 8.6 8.4 8.2 8.0 7.8 7.6 7.4 7.2 ppm Proton Chemical Shift (8) in ppm H2 H3 Н4 H5 H6 H7 H8 8.56
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 3 images

Blurred answer
Knowledge Booster
NMR Spectroscopy of Organic Molecules
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305080485
Author:
John E. McMurry
Publisher:
Cengage Learning
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning