Chapter 12: Q.9P (page 629)
Show the fragmentations that give rise to the peaks at m/z 43, 57, and 85 in the mass spectrum of 2,4-dimethylpentane (Figure 12-17).
Short Answer
Answer
Chapter 12: Q.9P (page 629)
Show the fragmentations that give rise to the peaks at m/z 43, 57, and 85 in the mass spectrum of 2,4-dimethylpentane (Figure 12-17).
Answer
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Get started for freeThree IR spectra are shown, corresponding to three of the following compounds. For each spectrum, determine the structure and explain how the peaks in the spectrum correspond to the structure you have chosen.
Account for the peaks at m/z 87, 111, and 126 in the mass spectrum of 2,6-dimethylheptan-4-ol.
Question: A common lab experiment is the dehydration of cyclopentanol tocyclopentene.
a. Explain how you could tell from the IR spectrum whether your product was pure cyclopentene, pure cyclopentanol or a mixture of cyclopentene and cyclopentanol. Give approximate frequencies for distinctive peaks.
b. Explain why mass spectrometry might not be a good way to distinguish cyclopentene from cyclopentanol.
Predict the masses and the structures of the most abundant fragments observed in the mass spectra of the following compounds
a. 2-methylpentane
b. 3-methylhex-2-ene
c. 4-methylpentane-2-ol
d. 2-methyl-1-phenylpropane
e. Cyclohexylisopropy; ether [cyclohexyl--O-CH(CH3)2 ]
f. CH3CH2CH2NHC(CH3)2
g.
h.3-bromo-2-methylpentane
For each spectrum, interpret all the significant streching frequencies above 1580 cm-10
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