Chapter 12: Q50E (page 385)
The infrared spectrum of the compound with the mass spectrum shown below has strong absorbances at 1584, 1478, and 1446 cm-1 . Propose a
structure consistent with the data.

Short Answer

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Chapter 12: Q50E (page 385)
The infrared spectrum of the compound with the mass spectrum shown below has strong absorbances at 1584, 1478, and 1446 cm-1 . Propose a
structure consistent with the data.


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-Carotene, a yellow food-coloring agent and dietary source of vitamin A can be prepared by a double Wittig reaction between 2 equivalents of-ionylideneacetaldehyde and a diylide. Show the structure of the -carotene product.

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: Propose structures for compounds that meet the following descriptions:
(a)with IR absorptions at 3300 and 2150
(b)with a strong IR absorption at 3400
(c) with a strong IR absorption at 1715
(d) with IR absorptions at 1600 and 1500
Question: The mass spectrum (a) and the infrared spectrum (b) of another unknown hydrocarbon are shown. Propose as many structures as you can.


Draw the structure of an alkene that yields only acetone, , on ozonolysis followed by treatment with Zn.
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