Chapter 16: Q13 P (page 502)
Draw resonance structures for the intermediates from the reaction of an electrophile at the ortho, meta, and para positions of nitrobenzene. Which intermediates are most stable?
Chapter 16: Q13 P (page 502)
Draw resonance structures for the intermediates from the reaction of an electrophile at the ortho, meta, and para positions of nitrobenzene. Which intermediates are most stable?
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Get started for freeWhich of the following alkyl halides would you expect to undergo Friedel–
Crafts reaction with rearrangement and which without? Explain.
(a)
(b)
(c)
(d)
(e) Chlorocyclohexane
At what position and on what ring do you expect nitration of 4-bromobiphenyl to occur? Explain, using resonance structures of the potentialintermediates.
Rank the compounds in each group according to their reactivity toward electrophilic substitution.
Melamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation for this reactivity.
Rank the following aromatic compounds in the expected order of their
reactivity toward Friedel–Crafts alkylation. Which compounds are
unreactive?
(a)Bromobenzene (b) Toluene (c) Phenol
(d)Aniline (e)Nitrobenzene (f)p-Bromotoluene
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