3. Consider the following stereoisomers of isopropyl methacrylate. Provide the expected number of peaks, the integrations of those peaks, the chemical shifts and the spliiting patterns expected for each. How are they different? b) Next to your description of the expected splitting pattern, please draw what that peak would look like. c) How could 1H NMR be used to determine the difference between these isomers? Please be specific.

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Explanation:

When there are two molecules then these molecules are described as stereoisomers if they are comprised of the same atoms associated in the same sequence, but the atoms are situated differently in the space. The disparity between stereoisomers can only be observed when the molecules is considered in a three-dimensional arrangement.

Kindly check the attached image below to the step by step explanation to the question above.

it would be d. henry moseley

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