Chapter 16: Q 4P (page 486)
Question: When benzene is treated with , deuterium slowly replaces all six hydrogens in the aromatic ring. Explain.
Short Answer

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Chapter 16: Q 4P (page 486)
Question: When benzene is treated with , deuterium slowly replaces all six hydrogens in the aromatic ring. Explain.

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Propose a mechanism for the reaction of 1-chloroanthraquinone with methoxide ion to give the substitution product 1-methoxyanthraquinone. Use curved arrows to show the electron flow in each step.

Question: Use your knowledge of directing effects, along with the following data, to deduce the directions of the dipole moments in aniline and bromobenzene.

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?
The following molecular model of a dimethyl-substituted biphenyl represents the lowest-energy conformation of the molecule. Why are the two benzene rings tilted at a 63° angle to each other rather than being in the same plane so that their p orbitals overlap? Why doesn’t complete rotation around the single bond joining the two rings occur?

How would you synthesize the following compound starting from benzene? More than one step is needed.

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