b) Given the structure of the hydrocarbon below:CH3CH2CIi.How many peaks will this compound produce in an NMR spectrumand why?ii.What will be the relative sizes of the peaks? Explainiii.Using the n+ 1 rule, how many splits will there be in each peak?

NMR is one of the spectroscopy method used for identification of compound.

b) Given the structure of the hydrocarbon below: CH3CH2CI i. How many peaks will this compound produce in an NMR spectrum and why? i. What will be the relative sizes of the peaks? Explain ii. Using the n+1 rule, how many splits will there be in each peak?

b) Given the structure of the hydrocarbon below: CH3CH2CI i. How many peaks will this compound produce in an NMR spectrum and why? i. What will be the relative sizes of the peaks? Explain ii. Using the n+1 rule, how many splits will there be in each peak?

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL4: Proton (1h) Nmr Spectroscopy

Section: Chapter Questions

Problem 8E

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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.

Question

b) Given the structure of the hydrocarbon below:
CH3CH2CI
i.
How many peaks will this compound produce in an NMR spectrum
and why?
ii.
What will be the relative sizes of the peaks? Explain
iii.
Using the n+ 1 rule, how many splits will there be in each peak?

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