Custom eBook for Organic Chemistry
Custom eBook for Organic Chemistry
2nd Edition
ISBN: 9798214171104
Author: Straumanis
Publisher: Cengage Custom
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Chapter L4, Problem 3E

Here are proton NMR data for 1-bromopropane: H a : triplet (2H) 3.32ppm; H b : multiplet (2H)1.81ppm; H c : triplet (3H) 0.93ppm. (Relative integrations shown in parentheses.)
a. Through how many bonds can a hydrogen split another hydrogen?
b. According to this splitting rule, does H a split H c ?
c. Is your answer in part a) consistent with the multiplicity listed for peak clusters a and c?
d. How many hydrogenssplit H b ?
e. Upon very close inspection of the proton NMR spectrum of 1-bromopropane, you wouldfind that peak cluster b has at least six peaks. Is this consistent with your answer in part d)?
f. Speculate as to why any peak cluster with more than four peaks is listed simply as a"multiplet."

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CH3 2. An unknown isomer of C4H9Cl has the ¹³C NMR and DEPT-135 spectra shown below: 13C NMR: 90 70 |||| A 50 8 (ppm) CH3CH₂CH₂ CH₂ CI 30 10 DEPT-135: CH3 CH3-CHCH₂-CI B 90 70 Circle the compound that is represented by these spectra. Clearly explain your reasoning. you will need to explain how each of the other three isomers was eliminated from consideration. 50 8 (ppm) CH3CH₂ CH-CI CH3 C 30 10 CH3 CH3-C-CI CH3 D
Which compound below fits the following proton NMR data? triplet 8 1.22 (3H) singlet d 1.98 (3H) quartet 8 4.07 (2H) OCH; A. CH3CH2COCH3 CHCOCH CH, PeHla D. CH;CCH2OCH3 B.H,C=C С. CH3
1.Assign an appropriate structure (B and C) to each spectrum (l and II) below. Briefly explain your answer. 2.Assign the proton signals of compound B and C in the 1H NMR spectrum respectively, based on your answer in 1.
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