Chapter 13: Q13-39E (page 419)
Predict the splitting pattern for each kind of hydrogen in isopropyl propanoate,.
Short Answer
Peaks produced are:
One singlet
Two quartet
Three septate
Four doublet
Chapter 13: Q13-39E (page 419)
Predict the splitting pattern for each kind of hydrogen in isopropyl propanoate,.
Peaks produced are:
One singlet
Two quartet
Three septate
Four doublet
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Get started for freePropose structures for compounds that fit the following descriptions:
(a) A hydrocarbon with seven lines in its 13C NMR spectrum
(b) A six-carbon compound with only five lines in its 13C NMR spectrum
(c) A four-carbon compound with three lines in its 13C NMR spectrum
Into how many peaks would you expect the 1H NMR signals of the indicated protons to be split? (Green=Cl.)
a)
b)
Propose structures for compounds that fit the following NMR data:
(a) C5H10O
0.95(6H,double, J = 7Hz)
2.10(3H,singlet)
2.43(1H, mutiplet)
(b) C3H5Br
2.32(3H,singlet)
5.35 (3H,singlet)
5.45(1H, broad signet )
The following 1H NMR absorptions were obtained on a spectrometer
operating at 300 MHz. Convert the chemical shifts from units to hertz
downfield from TMS.
(a)2.1(b)3.45(c)6.30(d)7.70
Question: The following1H NMR absorptions were obtained on a spectrometer
operating at 200 MHz and are given in hertz downfield from the TMS
standard. Convert the absorptions tounits.
(a)436 Hz(b)956 Hz(c)1504 Hz
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