Show how you would synthesize the following aromatic derivatives from benzene.
c. p-chlorotoluene
Show how you would synthesize the following aromatic derivatives from benzene.
c. p-chlorotoluene
Show how you would synthesize the following aromatic derivatives from benzene.
b. p-toluenesulfonic acid
Show how you would synthesize the following compounds, starting with benzene or toluene and any necessary acyclic reagents. Assume para is the major product (and separable from ortho) in ortho, para mixtures.
b. 1-phenyl-1-methoxybutane
Show how you would synthesize the following compounds, starting with benzene or toluene and any necessary acyclic reagents. Assume para is the major product (and separable from ortho) in ortho, para mixtures.
a. 1-phenyl-1-bromobutane
Starting from toluene, propose a synthesis of this trisubstituted benzene.
Propose a synthetic sequence of this trisubstituted benzene starting from toluene.
Show how you would synthesize the following aromatic derivatives from benzene.
a. p-tert-butylnitrobenzene
Acetaminophen is the active ingredient in Tylenol. How can acetominophen be synthesized from benzene?
Show how the following compounds can be prepared from benzene:
c.
Describe how 3-methyl-1-phenyl-3-pentanol can be prepared from benzene. You can use any inorganic reagents and solvents, and any organic reagents provided they contain no more than two carbons.
Benzene underwent a Friedel–Crafts acylation followed by a Wolff–Kishner reduction. The product gave the following 1H NMR spectrum. What acyl chloride was used in the Friedel–Crafts acylation?
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Beginning with benzene, synthesize the benzyl bromide shown.
Beginning with benzene, synthesize the following substituted benzenes. The ideal number of steps is indicated.
(d)
FROM THE LITERATURE The following steps were used in the synthesis of the antimalarial thiaplakortone A. Identify the missing reagents, (a) and (b),
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Provide the necessary reagents next to the arrows.