PROBLEM 28
Why is there no coupling between and or between and in cis- or trans-3-
chloropropenoic acid?
Let’s now summarize the kind of information that can be obtained from an
spectrum:
- The number of signals indicates the number of different kinds of protons that are
in the compound.
1 H NMR
Ha Hc Hb Hc
552 CHAPTER 14 NMR Spectroscopy
Coupling constants can be used to distinguish between the spectra of cis
and trans alkenes. The coupling constant of trans-vinylic protons is significantly
greater than the coupling constant of cis-vinylic protons (Figure 14.21), because the cou-
pling constant depends on the dihedral angle between the two bonds in the
unit. The coupling constant is greatest when the angle between
the two bonds is 180°(trans) and smaller when it is 0°(cis). Notice the differ-
ence between Jbdand Jcdin the spectrum of 3-bromo-1-propene (Figure 14.17).
C¬H
H¬C“C¬H
C¬H
1 H NMR
Table 14.3 Approximate Values of Coupling Constants
Approximate value of Jab (Hz) Approximate value of Jab (Hz)
C7
H
0
C
H
C
H
CC
H
H
H
C
C
C2
(geminal coupling)
H
15 (trans)
10 (cis)
1
(long-range
coupling)
ab
ab
a
b
a
Hb
C
C
H
C
C
b
Hb
C
Ha
C
Ha
ab
ab
a
b
b
b
a
a
a
b
b c
a
Jba = 14 Hz Jab = 14 Hz
c
a
Jba = 9 Hz Jab = 9 Hz
Hb Ha
C
H
Cl
COOH
H
C
b
C
H
Cl
C
H
COOH
Hb Ha
trans-3-chloropropenoic acid cis-3-chloropropenoic acid
Figure 14.21
The doublets observed for the and protons in the NMR spectra of trans-3-
chloropropenoic acid and cis-3-chloropropenoic acid. The coupling constant for trans
protons (14 Hz) is greater than the coupling constant for cis protons (9 Hz).
Ha Hb 1 H
The coupling contant for trans protons is
greater than the coupling constant for
cis protons.
The dependence of the coupling
constant on the angle between the two
bonds is called the Karplus
relationship after Martin Karplus,
who first observed the relationship.
Karplus was born in 1930. He
received a B.A. from Harvard
University and a Ph.D. from the
California Institute of Technology. He
is currently a professor of chemistry at
Harvard University.
C¬H