Describe the appearance of the 1H NMR spectrum of each of the following compounds. How many signals would you expect to find, and into how many peaks will each signal be split?
(a) ClCH2OCH2CH3
(b) CH3CH2OCH3
(c) CH3CH2OCH2CH3
(d) p-Diethylbenzene
(e) ClCH2CH2OCH2CH3
Sample Solution (a) Along with the triplet-quartet pattern of the ethyl group, the NMR spectrum of this compound will contain a singlet for the two protons of the chloromethyl group.
We need at least 10 more requests to produce the solution.
0 / 10 have requested this problem solution
The more requests, the faster the answer.