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 freeInto how many peaks would you expect the 1H NMR signals of the indicated protons to be split? (Green=Cl.)
a)
b)
Propose structures for the two compounds whose1H NMR spectra are
shown.
(a) C4H9Br
(b) C4H8CI2
Compound D is isomeric with compound C (Problem 13-61) and has the following NMR spectral data. Propose a structure.
Compound D Broadband-decoupled NMR: 9.7, 29.9, 74.4, 114.4, 141.4 d DEPT-90: 74.4, 141.4 d DEPT-135: positive peaks at 9.7, 74.4, 141.4 d; negative peaks at 29.9, 114.4 d
Classify the resonances in the13C NMR spectrum of methyl propanoate,.
2-Chloropropene shows signals for three kinds of protons in its 1H NMR spectrum. Explain.
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