Chapter 12: 35b E (page 385)
Question: At what approximate positions might the following compounds show
IR absorptions?
(b)
Short Answer
(b) It shows two distinguished absorption due to alkyne at 2100-2600 and at 3300.
Chapter 12: 35b E (page 385)
Question: At what approximate positions might the following compounds show
IR absorptions?
(b)
(b) It shows two distinguished absorption due to alkyne at 2100-2600 and at 3300.
All the tools & learning materials you need for study success - in one app.
Get started for freePropose structures for simple molecules that contain the following functional groups:
(a)Alcohol (b)Aromatic ring (c)Carboxylic acid (d)Amine (e)Both ketone and amine
(f) Two double bonds
Propose structures for compounds that fit the following mass-spectraldata:
(a) A hydrocarbon with M+= 132
(b) A hydrocarbon with M+=166
(c) A hydrocarbon with M+= 84
From what alkyne might each of the following substances have been made? (Green = Cl.)
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.
Question: Camphor, a saturated monoketone from the Asian camphor tree, is used among other things as a moth repellent and as a constituent of embalming
fluid. If camphor has M+=152.1201 by high-resolution mass spectrometry,
what is its molecular formula? How many rings does camphor
have?
What do you think about this solution?
We value your feedback to improve our textbook solutions.