Splitting of a signal in a proton NMR spectrum tells us the number of chemically non-equivalent hydrogens in the immediate vicinity of the hydrogen giving the signal. Predict the number of lines exhibited by hydrogens at the labeled positions in a first-order NMR spectrum. (Make the approximation that all coupling constants are equal.) 1) C CH₂ The number of lines exhibited by hydrogen(s) a is The number of lines exhibited by hydrogen(s) b is The number of lines exhibited by hydrogen(s) c is
Splitting of a signal in a proton NMR spectrum tells us the number of chemically non-equivalent hydrogens in the immediate vicinity of the hydrogen giving the signal. Predict the number of lines exhibited by hydrogens at the labeled positions in a first-order NMR spectrum. (Make the approximation that all coupling constants are equal.) 1) C CH₂ The number of lines exhibited by hydrogen(s) a is The number of lines exhibited by hydrogen(s) b is The number of lines exhibited by hydrogen(s) c is
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
ChapterL4: Proton (1h) Nmr Spectroscopy
Section: Chapter Questions
Problem 7E
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