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. The splitting abbreviations are s = singlet, d = doublet, t = triplet and q = quartet. Answer Bank d O 0 q 180 80 220 Incorrect q 200 160 140 120 100 60 40 d 20 CH3 H3C-C-NH₂ CH3 0

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. The splitting abbreviations are s = singlet, d = doublet, t = triplet and q = quartet. Answer Bank d O 0 q 180 80 220 Incorrect q 200 160 140 120 100 60 40 d 20 CH3 H3C-C-NH₂ CH3 0

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL3: Carbon (13c) Nmr Spectroscopy

Section: Chapter Questions

Problem 7CTQ

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