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

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Choose the most intense mass spectrum signal for 12 m/z 29 m/z 41 m/z 57 m/z А D
(a) What would be the chemical shift of a peak that is observed at 655.2 Hz from the reference tetramethylsilane (TMS) recorded using a 90 MHz spectrometer ? (b) At what frequency would the chemical shift of chloroform (CHCl3, δ = 7.28 ppm) occur relative to TMS on a spectrum recorded on a 300 MHz spectrometer? (c) At what frequency and chemical shift would the signal for chloroform occur when using a 1 GHz NMR spectrometer?
The mass spectrum of an unknown compound has a molecular ion peak with a relative intensity of 52.18% and an M+1 peak of 3.37%. How many carbon atoms are in the compound? (Fill in an integer number)
#6) Using the following spectra and other information provided, identify the compound. Assign pertinent peaks in the spectra. Label the peaks on the spectrum and place the structure of the compound in the box on the right side of the spectrum - Identify correct compound - label proton spectrum - label carbon spectrum
Methine protons are ___ shielded and ____ electron-rich than methylene and methyl protons. less, less less, more more, more more, less 2.How many protons give rise to the signal at 1.60 ppm if the molecular formula is C10H20O2?
Identify the following spectra. Please find peaks are assigned on the spectrum (~5-6 peaks). Label the peaks on the spectrum and place the structure of the compound in the box on the lower left-hand corner of the spectrum (from the table below, no numbering scheme). You do not have to indicate the exact wavenumber of the peak.
I need help solving 3
Calculate the exact resonance frequency for the two signals of 1,3-dichloropropane B = 3.75 Cl-C- C-C- B JAB=6.2 Hz A = 2.20 TMS 90 Hz, ア 6 5 4 2 1 O ô ppm I-0-IM I-U-IA I-y-IB
For the dimedone molecule, how many different signals would you see in the proton NMR? Assume you can see them all
Help me find the 13C NMR spectrum of the image
#3) Using the following spectra and other information provided, identify the compound. Assign pertinent peaks in the spectra. Label the peaks on the spectrum and place the structure of the compound in the box on the right side of the spectrum - Identify correct compound - label proton spectrum - label carbon spectrum
#5) Using the following spectra and other information provided, identify the compound. Assign pertinent peaks in the spectra. Label the peaks on the spectrum and place the structure of the compound in the box on the right side of the spectrum - Identify correct compound - label proton spectrum - label carbon spectrum