Chapter 16: Q74E (page 524)
Question: Identify the reagents represented by the letters a–e in the following scheme:
Chapter 16: Q74E (page 524)
Question: Identify the reagents represented by the letters a–e in the following scheme:
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Get started for freePropose 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.
Rank the compounds in each of the following groups in order of their reactivity
to electrophilic substitution:
(a) Nitrobenzene, phenol, toluene, benzene
(b) Phenol, benzene, chlorobenzene, benzoic acid
(c) Benzene, bromobenzene, benzaldehyde, aniline
How would you synthesize the following compound starting from benzene? More than one step is needed.
4- chloropyridine undergoes reaction with dimethylamine to yield 4-dimethylaminopyridine. Propose a mechanism for the reaction.
You know the mechanism of HBr addition to alkenes, and you know the effects of various substituent groups on aromatic substitution. Use this knowledge to predict which of the following two alkenes reacts faster with HBr. Explain your answer by drawing resonance structures of the carbocation intermediates.
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