Chapter 12: Q12-35d E (page 385)
At what approximate positions might the following compounds showIR absorptions?
(d)

Short Answer
(d) It shows one distinguishing absorption due to ester at 1735.
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Chapter 12: Q12-35d E (page 385)
At what approximate positions might the following compounds showIR absorptions?
(d)

(d) It shows one distinguishing absorption due to ester at 1735.
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Question: At what approximate positions might the following compounds show
IR absorptions?
(b)

Question: The infrared spectrum of the compound with the mass spectrum shown below lacks any significant absorption above . There is a prominent peak near and another strong peak near .Propose a structure consistent with the data.

Identify the functional groups in each of the following molecules:
(a) Methionine, an amino acid:

(b)Ibuprofen, a pain reliever:

(c) Capsaicin, the pungent substance in chili peppers:

Question: The nitrogen ruleof mass spectrometry says that a compound containing an odd number of nitrogen’s has an odd-numbered molecular ion.
Conversely, a compound containing an even number of nitrogen’s has
an even-numbered M+peak. Explain.
Question: Two infrared spectra are shown. One is the spectrum of cyclohexane,
and the other is the spectrum of cyclohexene. Identify them, and
explain your answer.
(a)

(b)

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