Chapter 14: Q.21558-14-3P. (page 533)
How many 1H NMR signals does each compound show?
a.
b.
c.
d.
e.
f.
g.
h.
Short Answer
a. 2
b. 2
c. 2
d. 2
e. 4
f. 4
g. 5
h. 4
Chapter 14: Q.21558-14-3P. (page 533)
How many 1H NMR signals does each compound show?
a.
b.
c.
d.
e.
f.
g.
h.
a. 2
b. 2
c. 2
d. 2
e. 4
f. 4
g. 5
h. 4
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Get started for freeQuestion: Identify the carbon atoms that give rise to the signals in the 13C NMR spectrum of each compound.
a. CH3CH2CH2CH2OH ; 13CNMR: 14, 19, 35, and 62 ppm
b. (CH3)2CHCHO ; 13C NMR: 16, 41, and 205 ppm
c. CH2=CHCHOHCH3 ; 13C NMR: 23, 69, 113, and 143 ppm
Question: How many \(^{\bf{1}}{\bf{H}}\) NMR signals does each compound give?
a.
b.
c.
d.
a.
b.
c.
d.
e.
f.
g.
h.
Which compounds give a 1H NMR spectrum with two signals in a ratio of 2:3?
a.
b.
c.
d.
How many peaks are observed in the 1HNMR signal for each proton shown in red in palau'amine, the complex chapter-opening molecule?
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