Construct a simulated 1H NMR spectrum for 1,2-dichloroethane by dragging and dropping the appropriate splitting pattern into the box on the chemical shift baseline, and by dragging an integration value into the small box above the signal. Peak heights do not represent integration.

All hydrogens are in same environment. Hence it will not split which shows as singlet for 4 hydrogen

Explanation:

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you did not give any options thus this is the best answer i can give to you with this little information you have given

> they are both natural and not man made

> they can be tracked and predicted by the right tools

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