Chapter 14: Q.21558-14-16P. (page 546)
Sketch the NMR spectrum of CH3CH2Cl , giving the approximate location of each NMR signal.
Chapter 14: Q.21558-14-16P. (page 546)
Sketch the NMR spectrum of CH3CH2Cl , giving the approximate location of each NMR signal.
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Get started for freeQuestion:Answer the following questions about each of the hydroxy ketones: 1-hydroxybutan-2-one (A) and 4-hydroxybutan-2-one (B).
a. What is the molecular ion in the mass spectrum?
b. What IR absorptions are present in the functional group region?
c. How many lines are observed in the 13C NMR spectrum?
d. How many signals are observed in the 1H NMR spectrum?
e. Give the splitting observed for each type of proton as well as its approximate chemical shift.
Question: 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?
a.
b.
Into how many peaks will each proton shown in green be split?
a.
b.
c.
d.
e.
f.
Draw a splitting diagram for Hb in trans-1,3-dichloropropene, given that Jab = 13.1 Hz and Jbc = 7.2 Hz.
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