Chapter 12: Q13P (page 354)
Show how you could prepare the following compounds from 4-methyl-3- penten-2-one,
(a)
(b)
(c)
Short Answer
(a)
Formation of the desired product
(b)
Formation of the desired product
(c)
Formation of the desired product
Chapter 12: Q13P (page 354)
Show how you could prepare the following compounds from 4-methyl-3- penten-2-one,
(a)
(b)
(c)
(a)
Formation of the desired product
(b)
Formation of the desired product
(c)
Formation of the desired product
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Get started for freeQuestion: How would you use infrared spectroscopy to distinguish between thefollowing pairs of constitutional isomers?
(a)
(b)
(c)
Question: The infrared spectrum of the compound with the mass spectrum shown below has strong absorbances at 1584, 1478, and . Propose astructure consistent with the data.
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
Write molecular formulas for compounds that show the following molecularions in their high-resolution mass spectra, assuming that C, H, N,and O might be present. The exact atomic masses are: 1.00783(1H), 12.00000(12C) , 14.00307 (14N) , 15.99491(16O) .
(a) M+ = 98.0844
(b) M+= 123.0320
What functional groups might the following molecules contain?
(a) A compound with a strong absorption at 1710 cm-1
(b) A compound with a strong absorption at 1540 cm-1
(c) A compound with strong absorptions at 1720 cm-1 and 2500 to 3100cm-1
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