Chapter 15: Q15-3P (page 455)
Draw structures corresponding to the following IUPAC names:
(a) p-Bromochlorobenzene
(b) p-Bromotoluene
(c) m-Chloroaniline
(d) 1-Chloro-3,5-dimethylbenzene
Chapter 15: Q15-3P (page 455)
Draw structures corresponding to the following IUPAC names:
(a) p-Bromochlorobenzene
(b) p-Bromotoluene
(c) m-Chloroaniline
(d) 1-Chloro-3,5-dimethylbenzene
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Get started for freeIn 1932, A. A. Levine and A. G. Cole studied the ozonolysis of o-xylene and isolated three products: glyoxal, 2,3-butanedione, and pyruvaldehyde:
In what ratio would you expect the three products to be formed if o-xylene is a resonance hybrid of two structures? The actual ratio found was 3 parts glyoxal, 1 part 2,3-butanedione, and 2 parts pyruvaldehyde. What conclusions can you draw about the structure of o-xylene?
How might you convert 1, 3, 5, 7-cyclononatetraene to an aromatic substance?
Give IUPAC names for the following compounds:
On reaction with acid, 4-pyrone is protonated on the carbonyl-group oxygen to give a stable cationic product. Using resonance structures and the Hückel’s rule, explain why the protonated product is so stable.
4-Pyrone
Draw and name all possible aromatic compounds with the formula C8H9Br.
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