Chapter 14: Q9P (page 527)
Question: For each compound, first label each different type of proton and then rank the protons in order of increasing chemical shift.
a.
b.
c.
Short Answer
a.
b.
c.
Chapter 14: Q9P (page 527)
Question: For each compound, first label each different type of proton and then rank the protons in order of increasing chemical shift.
a.
b.
c.
a.
b.
c.
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Get started for freeEsters of chrysanthemic acid are naturally occurring insecticides. How many lines are present in the NMR spectrum of chrysanthemic acid?
Question: A compound of molecular formula C4H802 shows no IR peaks at 3600–3200 or 1700 cm-1 . It exhibits one singlet in its 1H NMR spectrum at 3.69 ppm, and one line in its 13C NMR spectrum at 67 ppm. What is the structure of this unknown?
Question: 18-Annulene shows two signals in its 1 H NMR spectrum, one at 8.9 (12 H) and one at –1.8 (6 H) ppm. Using a similar argument to that offered for the chemical shift of benzene protons, explain why both shielded and deshielded values are observed for 18-annulene.
Label each statement as True or False.
a. When a nucleus is strongly shielded, the effective field is larger than the applied field and the absorption shifts downfield.
b. When a nucleus is strongly shielded, the effective field is smaller than the applied field and the absorption is shifted upfield.
c. A nucleus that is strongly deshielded requires a lower field strength for resonance.
d. A nucleus that is strongly shielded absorbs at a larger δ value.
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