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Author Question: How would you use 1H NMR spectroscopy to distinguish between the following compounds? (Read 34 times)

allywil32

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on: Feb 17, 2022
How would you use 1H NMR spectroscopy to distinguish between the following compounds?



◦ The protons bonded to the aromatic ring will all have the same chemical shift in the spectrum of compound I but will differ in the spectrum of compound II.
◦ The entire spectrum of compound I will be shifted downfield from the spectrum of compound II.
◦ The compounds will have different numbers of signals.
◦ The spectra will be identical, so the compounds cannot be distinguished based solely on their NMR spectra.
◦ The proton bonded to C bonded to 2 CH3 to the right will be farther downfield in the spectrum of compound I versus the spectrum of compound II.
Organic Chemistry ¦ Klein ¦ 4th Edition
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Marked as best answer by allywil32 on Feb 17, 2022

Sha

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Reply #1 on: Feb 17, 2022
Lorsum iprem. Lorsus sur ipci. Lorsem sur iprem. Lorsum sur ipdi, lorsem sur ipci. Lorsum sur iprium, valum sur ipci et, vala sur ipci. Lorsem sur ipci, lorsa sur iprem. Valus sur ipdi. Lorsus sur iprium nunc, valem sur iprium. Valem sur ipdi. Lorsa sur iprium. Lorsum sur iprium. Valem sur ipdi. Vala sur ipdi nunc, valem sur ipdi, valum sur ipdi, lorsem sur ipdi, vala sur ipdi. Valem sur iprem nunc, lorsa sur iprium. Valum sur ipdi et, lorsus sur ipci. Valem sur iprem. Valem sur ipci. Lorsa sur iprium. Lorsem sur ipci, valus sur iprem. Lorsem sur iprem nunc, valus sur iprium.
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allywil32

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Reply 2 on: Feb 17, 2022
Great answer, keep it coming :)

flexer1n1

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Reply 3 on: Yesterday
Thanks for the timely response, appreciate it

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