Chapter 14: Q3P (page 527)
Question: How many \(^{\bf{1}}{\bf{H}}\) NMR signals does each compound show?
a.
b.
c.
d.
e.
f.
g.
h.
Short Answer
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Chapter 14: Q3P (page 527)
Question: How many \(^{\bf{1}}{\bf{H}}\) NMR signals does each compound show?
a.
b.
c.
d.
e.
f.
g.
h.
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b.
c.
d.
e.
f.
g.
h.
i.
j.
What splitting pattern is observed for each proton in the following compounds?
a.
b.
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?
Which of the highlighted carbon atoms in each molecule absorbs farther downfield?
a.
b.
c.
d.
Esters of chrysanthemic acid are naturally occurring insecticides. How many lines are present in the NMR spectrum of chrysanthemic acid?
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