Chapter 14: Q.21558-14-7P. (page 535)
How many NMR signals would you expect for each compound?
a.
b.
c.
Short Answer
a. 4
b. 5
c. 5
Chapter 14: Q.21558-14-7P. (page 535)
How many NMR signals would you expect for each compound?
a.
b.
c.
a. 4
b. 5
c. 5
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Get started for freePropose a structure consistent with each set of data.
a. C9H10O2: IR absorption at 1718cm-1
b. C9H12 : IR absorption at 2850–3150cm-1
Question: As we will learn in Chapter 20, reaction of (CH3)2CO with followed by affords compound D, which has a molecular ion in its mass spectrum at 84 and prominent absorptions in its IR spectrum at 3600–3200, 3303, 2938, and 2120cm-1 . D shows the following 1 H NMR spectral data: 1.53 (singlet, 6 H), 2.37 (singlet, 1 H), and 2.43 (singlet, 1 H) ppm. What is the structure of D?
Question: How many \(^{\bf{1}}{\bf{H}}\) NMR signals does each compound show?
a.
b.
c.
d.
e.
f.
g.
h.
How many lines are observed in the \({}^{{\bf{13}}}{\bf{C}}\) NMR spectrum of each compound?
a.
b.
c.
d.
What protons in alcohol A give rise to each signal in its 1HNMR spectrum? Explain all splitting patterns observed for absorptions between 0–7 ppm.
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