Chapter 16: Q29E (page 524)
The sulfonation of an aromatic ring with is reversible. That is, heating benzenesulfonic acid with H2SO4 yields benzene. Show the mechanism of the desulfonation reaction. What is the electrophile?
Chapter 16: Q29E (page 524)
The sulfonation of an aromatic ring with is reversible. That is, heating benzenesulfonic acid with H2SO4 yields benzene. Show the mechanism of the desulfonation reaction. What is the electrophile?
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Get started for freeDraw resonance structures of the intermediate carbocations in the bromination of naphthalene, and account for the fact that naphthalene undergoes electrophilic substitution at C1 rather than C2.
Phenols (ArOH) are relatively acidic, and the presence of a substituent group on the aromatic ring has a large effect. The of unsubstituted phenol, for example, is 9.89, while that of p-nitrophenol is 7.15. Draw resonance structures of the corresponding phenoxide anions and explain the data.
At what position would you expect electrophilic substitution to occur in each of the following substances?
a.
b.
c.
The N,N,N-trimethylammonium group , is one of the few groups that is a meta-directing deactivator yet has no electron-withdrawing resonance effect. Explain
What aromatic products would you obtain from the oxidation of the following substances?
a.
b.
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