Construct a simulated proton-decoupled 13C NMR spectrum for tert-butylamine. Drag the resonance signal to the appropriate chemical shift positions. Then label the box above each signal with the expected splitting if there were no proton decoupling. CH3 NH₂ H3C t S d ** 220 200 140 120 100 80 60 40 20 0 CH3 180 160

Construct a simulated proton-decoupled 13C NMR spectrum for tert-butylamine. Drag the resonance signal to the appropriate chemical shift positions. Then label the box above each signal with the expected splitting if there were no proton decoupling. CH3 NH₂ H3C t S d ** 220 200 140 120 100 80 60 40 20 0 CH3 180 160

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy

Section13.3: The Chemical Shift

Problem 4P: The following 1H NMR peaks were recorded on a spectrometer operating at 200 MHz. Convert each into...

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