Chapter 14: Q9P (page 527)
Question: For each compound, first label each different type of proton and then rank the protons in order of increasing chemical shift.
a.
b.
c.
Short Answer
a.
b.
c.
Chapter 14: Q9P (page 527)
Question: For each compound, first label each different type of proton and then rank the protons in order of increasing chemical shift.
a.
b.
c.
a.
b.
c.
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Get started for freeQuestion: The \(^{\bf{1}}{\bf{H}}\) NMR spectrum 1,2-dimethoxyethane \(\left( {{\bf{C}}{{\bf{H}}_{\bf{3}}}{\bf{OC}}{{\bf{H}}_{\bf{2}}}{\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{OC}}{{\bf{H}}_{\bf{3}}}} \right)\) recorded on a 300 MHz NMR spectrometer consists of signals at 1017 Hz and 1065 Hz downfield from TMS. (a) Calculate the chemical shift of each absorption. (b) At what frequency would each absorption occur if the spectrum were recorded on a 500 MHz NMR spectrometer?
Question. Reaction of aldehyde D with amino alcohol E in the presence of NaH forms F (molecular formula C11H15NO2). F absorbs at 1730 cm-1in its IR spectrum. F also shows eight lines in its 13C-NMR spectrum, and gives the following -NMR spectrum: 2.32 (singlet, 6 H), 3.05 (triplet, 2 H), 4.20 (triplet, 2 H), 6.97 (doublet, 2 H), 7.82 (doublet, 2 H), and 9.97 (singlet, 1 H) ppm. Propose a structure for F. We will learn about this reaction in Chapter 18.
The 1H NMR spectrum of CH3OH recorded on a 500 MHz NMR spectrometer consists of two signals, one due to the CH3 protons at 1715 Hz and one due to the OH proton at 1830 Hz, both measured downfield from TMS. (a) Calculate the chemical shift of each absorption. (b) Do the CH3 protons absorb upfield or downfield from the OH proton?
Esters of chrysanthemic acid are naturally occurring insecticides. How many lines are present in the \({}^{{\bf{13}}}{\bf{C}}\) NMR spectrum of chrysanthemic acid?
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