Chapter 12: Q35d E (page 385)
At what approximate positions might the following compounds show
IR absorptions?
Short Answer
(d) It shows one distinguishing absorption due to ester at 1735
Chapter 12: Q35d E (page 385)
At what approximate positions might the following compounds show
IR absorptions?
(d) It shows one distinguishing absorption due to ester at 1735
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Get started for freeThe 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.
Draw the structure of an alkene that yields only acetone, , on ozonolysis followed by treatment with Zn.
Question: 4-Methyl-2-pentanone and 3-methylpentanal are isomers. Explain how you could tell them apart, both by mass spectrometry and by infrared spectroscopy.
The heat of hydrogenation for allene (Problem 7-61) to yield propane is -295 kJ/mol, and the heat of hydrogenation for a typical monosubstituted alkene, such as propene, is -125 kJ/mol. Is allene more stable or less stable than you might expect for a diene? Explain.
Most stable organic species have tetravalent carbon atoms, but species with trivalent carbon atoms also exist. Carbocations are one such class of compounds.
(a) How many valence electrons does the positively charged carbon atom have?
(b) What hybridization do you expect this carbon atom to have?
(c) What geometry is the carbocation likely to have?
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