Question
The 1 H-NMR spectrum of 2-(2-bromoethyl)-1,3-dioxolane (at o right) shows a 2H signal near 2 ppm (far right). (a) What would you call this pattern?
The 1 H-NMR spectrum of 2-(2-bromoethyl)-1,3-dioxolane (at o right) shows a 2H signal near 2 ppm (far right).
(a) What would you call this pattern?
(b) Which hydrogen(s) gave rise to this signal?
(c) Draw a splitting tree corresponding to this pattern.
-Br
Step by Step Solution
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Circled CH2 group protons gives a quartet signal near 20 ppm ...
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Organic Chemistry
Authors: Graham Solomons, Craig Fryhle, Scott Snyder
11th edition
1118133579, 978-1118133576
