Chapter 12: Q-12-12-50E (page 385)
Question: The infrared spectrum of the compound with the mass spectrum shown below has strong absorbances at 1584, 1478, and . Propose a
structure consistent with the data.
Chapter 12: Q-12-12-50E (page 385)
Question: The infrared spectrum of the compound with the mass spectrum shown below has strong absorbances at 1584, 1478, and . Propose a
structure consistent with the data.
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Get started for freeBeginning with acetylene and any alkyl halide needed, how would you synthesize the following compounds?
(a)Decane
(b)2,2-Dimethylhexane
(c)Hexanal
(d)2-Heptanone
Question: Halogenated compounds are particularly easy to identify by their mass
spectra because both chlorine and bromine occur naturally as mixtures
of two abundant isotopes. Recall that chlorine occurs as 35Cl (75.8%)
and 37C (24.2%); and bromine occurs as 79Br (50.7%) and 81Br (49.3%).
At what masses do the molecular ions occur for the following formulas?
What are the relative percentages of each molecular ion?
(a)Bromomethane, CH3Br
(b)1-Chlorohexane, C6H13Cl
Where might the following compound have IR absorptions?
Aprobarbital, a barbiturate once used in treating insomnia, is synthesized in three steps from diethyl malonate. Show how you would synthesize the necessary dialkylated intermediate, and then propose a mechanism for the reaction of this intermediate with urea to give aprobarbital.
Question: The mass spectrum (a) and the infrared spectrum (b) of another unknown hydrocarbon are shown. Propose as many structures as you can.
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