Q6. Complete Table 6. i) Copy and paste (insert) the correct alternative of thestructures below into the table, ii) insert expected number of different ¹H and 1³Cenvironments expected for these compounds (Table 6: columns 2 and 3 respectively)and correctly label the ¹H and ¹³C NMR spectra below in boxes provided.CICITable 6: Assigning NMR spectra for aromaticStructures of disubstitutedNo. of expected ¹HNMR peak/sbenzene compounds1,2-dichorobenzene1,3-dichorobenzene.CI1,4-dichorobenzeneCIcompoundsNo. of expected ¹³℃NMR peak/s

NMR is branch of chemistry in which we deal with shielding and deshielding effect of protons.

Copy and paste (insert) the correct alterna able, ii) insert expected number of different r these compounds (Table 6: columns 2 a and 13C NMR spectra below in boxes prov .CI CI ng NMR spectra for aromatic compo

Copy and paste (insert) the correct alterna able, ii) insert expected number of different r these compounds (Table 6: columns 2 a and 13C NMR spectra below in boxes prov .CI CI ng NMR spectra for aromatic compo

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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Concept explainers

Mass Spectrometry

This process is an instrumental method in which a sample is changed to fast moving positive ions by electron bombardment. The charged particles vary due to their different mass to charge ratio and are estimated with the help of this difference. It is also called mass spectroscopy.

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Q6. Complete Table 6. i) Copy and paste (insert) the correct alternative of the
structures below into the table, ii) insert expected number of different ¹H and 1³C
environments expected for these compounds (Table 6: columns 2 and 3 respectively)
and correctly label the ¹H and ¹³C NMR spectra below in boxes provided
.CI
CI
Table 6: Assigning NMR spectra for aromatic
Structures of disubstituted
No. of expected ¹H
NMR peak/s
benzene compounds
1,2-dichorobenzene
1,3-dichorobenzene
.CI
1,4-dichorobenzene
CI
compounds
No. of expected ¹³℃
NMR peak/s

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