Question- 1. 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.
2. Construct a simulated proton-decoupled 13C NMR spectrum for tert-butyl alcohol. Drag the resonance signal icon to the appropriate chemical shift positions. Then label the box above each resonance signal with the corresponding number of equivalent carbons. (Not all chemical shift bins will be used.)
Please take care to answer the question as mark are equally granted for each point