Chapter 14: Q30P (page 527)
Which of the highlighted carbon atoms in each molecule absorbs farther downfield?
a.
b.
c.
d.
Short Answer
a.
b.
c.
d.
Chapter 14: Q30P (page 527)
Which of the highlighted carbon atoms in each molecule absorbs farther downfield?
a.
b.
c.
d.
a.
b.
c.
d.
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Get started for freeEsters of chrysanthemic acid are naturally occurring insecticides. How many lines are present in the \({}^{{\bf{13}}}{\bf{C}}\) NMR spectrum of chrysanthemic acid?
Propose a structure consistent with each set of data.
a. Compound J: molecular ion at 72; IR peak at 1710cm-1 ; 1H -NMR data (ppm) at 1.0 (triplet, 3 H), 2.1 (singlet, 3 H), and 2.4 (quartet, 2 H)
b. Compound K: molecular ion at 88; IR peak at 3600โ3200 ;1H-NMR data (ppm) at 0.9 (triplet, 3 H), 1.2 (singlet, 6 H), 1.5 (quartet, 2 H), and 1.6 (singlet, 1 H)
Question. Compound O has a molecular formula C10H12O and shows an IR absorption at 1687 . The 1H -NMR spectrum of O is given below. What is the structure of O?
a.
b.
How many NMR signals does each compound give?
a.
b.
c.
d.
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