Multiple Choice Rank the following in order of increasing rate of electrophilic aromatic bromination (slowest to fastest). 350views
Textbook Questionp-Xylene undergoes nitration much faster than benzene. Use resonance forms of the sigma complex to explain this accelerated rate826views
Textbook QuestionFor each horizontal row of substituted benzenes, indicate a. the one that is the most reactive in an electrophilic aromatic substitution reaction. 459views
Textbook QuestionList the compounds in each set from most reactive to least reactive toward electrophilic aromatic substitution: b. dichloromethylbenzene, difluoromethylbenzene, toluene, chloromethylbenzene491views
Textbook QuestionList the compounds in each set from most reactive to least reactive toward electrophilic aromatic substitution: a. benzene, phenol, toluene, nitrobenzene, bromobenzene1131views1rank
Textbook QuestionRank each group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: b. 1-chloro-2,4-dinitrobenzene, 2,4-dinitrophenol, 1-methyl-2,4-dinitrobenzene435views
Textbook QuestionRank each group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: e. p-methylnitrobenzene, 2-chloro-1-methyl-4-nitrobenzene, 1-methyl-2,4-dinitrobenzene, p-chloromethylbenzene465views
Textbook QuestionRank each group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: f. bromobenzene, chlorobenzene, fluorobenzene, iodobenzene528views
Textbook QuestionFor each horizontal row of substituted benzenes, indicate b. the one that is the least reactive in an electrophilic aromatic substitution reaction.413views
Textbook QuestionFor each horizontal row of substituted benzenes, indicate b. the one that is the least reactive in an electrophilic aromatic substitution reaction.415views
Textbook QuestionWhy is anisole nitrated more rapidly than thioanisole under the same conditions?502views
Textbook QuestionA mixture of 0.10 mol benzene and 0.10 mol p-xylene was allowed to react with 0.10 mol nitronium ion until all the nitronium ion was gone. Two products were obtained: 0.002 mol of one and 0.098 mol of the other. b. Why was more of one product obtained than of the other?320views
Textbook Question(••) Indigo is a dye that was originally isolated from coal tar. In 1905, Johann Friedrich Wilhelm Adolf von Baeyer won a Nobel Prize for a method that allowed indigo to be isolated from plants [a green chemist ahead of his time.] If you nitrated indigo using the reaction learned in this chapter, at which carbon would you expect the nitro group to attach?<IMAGE> 348views
Textbook QuestionSubstitution at the benzylic position of the molecules shown was observed to occur at different rates. Explain this observation.372views
Textbook QuestionPredict the mononitration products of the following compounds.(d) p-methoxybenzoic acid230views
Textbook QuestionPredict the mononitration products of the following compounds.(e) m-cresol (m-methylphenol)228views
Textbook QuestionPredict the mononitration products of the following compounds.(f) o-hydroxyacetophenone250views
Textbook QuestionAre the following substituents ortho–para directors or meta directors? d. COOH e. CF3 f. N=O431views
Textbook QuestionUsing resonanOce contributors for the carbocation intermediate, explain why a phenyl group is an ortho–para director.352views
Textbook QuestionFor each of the following compounds, indicate the ring carbon(s) that is/are nitrated when the compound is treated with HNO3/H2SO4: e. f.423views
Textbook Questiona. Does a coupling reaction have to be used to synthesize p-dipropylbenzene? b. Can a coupling reaction be used to synthesize p-dipropylbenzene?423views
Textbook QuestionWhat products are obtained from the reaction of the following compounds with one equivalent of Br2, using FeBr3 as a catalyst? c. d. 536views
Textbook QuestionRank the following compounds from most reactive to least reactive in an electrophilic aromatic substitution reaction: <s>831views
Textbook QuestionFor each of the statements in Column I, choose a substituent from Column II that fits the description for the compound on the right:347views
Textbook QuestionPredict the major products of bromination of the following compounds, using Br2 and FeBr3 in the dark. (a) 1089views1rank
Textbook QuestionPredict the major products of bromination of the following compounds, using Br2 and FeBr3 in the dark. (b) 1191views1rank1comments
Textbook QuestionPredict the major products of bromination of the following compounds, using Br2 and FeBr3 in the dark. (C) 1198views
Textbook QuestionPredict the major products formed when benzene reacts (just once) with the following reagents. (f) fuming sulfuric acid1075views
Textbook QuestionBiphenyl is two benzene rings joined by a single bond. The site of substitution for a biphenyl is determined by (1) which phenyl ring is more activated (or less deactivated), and (2) which position on that ring is most reactive, using the fact that a phenyl substituent is activating and ortho, para-directing. (a) Use resonance forms of a sigma complex to show why a phenyl substituent should be ortho, para-directing.2159views
Textbook QuestionBiphenyl is two benzene rings joined by a single bond. The site of substitution for a biphenyl is determined by (1) which phenyl ring is more activated (or less deactivated), and (2) which position on that ring is most reactive, using the fact that a phenyl substituent is activating and ortho, para-directing. (b) Predict the mononitration products of the following compounds. (iv) 663views
Textbook QuestionBiphenyl is two benzene rings joined by a single bond. The site of substitution for a biphenyl is determined by (1) which phenyl ring is more activated (or less deactivated), and (2) which position on that ring is most reactive, using the fact that a phenyl substituent is activating and ortho, para-directing. (b) Predict the mononitration products of the following compounds. (v) 633views
Textbook QuestionBiphenyl is two benzene rings joined by a single bond. The site of substitution for a biphenyl is determined by (1) which phenyl ring is more activated (or less deactivated), and (2) which position on that ring is most reactive, using the fact that a phenyl substituent is activating and ortho, para-directing. (b) Predict the mononitration products of the following compounds. (vi) 1441views1rank
Textbook QuestionStep 2 of the iodination of benzene shows water acting as a base and removing a proton from the sigma complex. We did not consider the possibility of water acting as a nucleophile and attacking the carbocation, as in an electrophilic addition to an alkene. Draw the reaction that would occur if water reacted as a nucleophile and added to the carbocation. Explain why this type of addition is rarely observed.865views1rank
Textbook QuestionPropose a mechanism for the sulfonation of pyridine, and point out why sulfonation occurs at the 3-position.1216views2rank
Textbook QuestionShow how m-toluidine can be converted to the following compounds, using any necessary reagents. (e) 598views
Textbook Question(••••) The first step of a reaction called electrophilic aromatic substitution (see Chapter 23) is as follows: <IMAGE>If this step is rate-determining for the overall reaction, which benzene derivative would you expect to react most quickly? Which would react most slowly? [Use the information you gleaned from working Assessments 14.55–14.59.](a) <IMAGE>322views
Textbook QuestionThe nitro group directs electrophilic aromatic substitution to the meta position. After reduction by hydrogenation, to which carbon(s) does it direct?<IMAGE>369views1rank
Textbook QuestionPredict the major product of the following electrophilic aromatic substitution reactions.(b) <IMAGE> 408views
Textbook QuestionPredict the major products formed when benzene reacts (just once) with the following reagents. (i) iodine + HNO3495views
Textbook QuestionPredict the major products formed when benzene reacts (just once) with the following reagents. (d) bromine + a nail772views
Textbook QuestionDraw the product(s) of each of the following reactions: a. benzoic acid + HNO3/H2SO4 b. isopropylbenzene + Cl2 + FeCl3642views
Textbook QuestionWhat is the major product(s) of each of the following reactions? e. nitration of p-methoxybenzaldehyde f. nitration of p-tert-butylmethylbenzene445views
Textbook QuestionPredict the mononitration products of the following compounds. (a) o-nitrotoluene (b) m-chlorotoluene (c) o-bromobenzoic acid997views1rank
Textbook QuestionGive the products, if any, of each of the following reactions: a. benzonitrile + methyl chloride + AlCl3 b. phenol + Br2665views
Textbook QuestionGive the products, if any, of each of the following reactions: c. benzoic acid + CH3CH2Cl + AlCl3 d. benzene + 2 CH3Cl + AlCl3500views
Textbook QuestionPredict the major products formed when benzene reacts (just once) with the following reagents. (g) 1-chloro-2,2-dimethylpropane + AlCl3677views
Textbook QuestionPropose products (if any) and mechanisms for the following AlCl3-catalyzed reactions: (c) 3-chloro-2,2-dimethylbutane with isopropylbenzene1828views
Textbook QuestionPredict the products (if any) of the following reactions. (a) (excess) benzene + isobutyl chloride + AlCl3851views
Textbook QuestionPredict the products (if any) of the following reactions. (b) (excess) toluene + butan-1-ol + BF31629views
Textbook QuestionWhich reactions will produce the desired product in good yield? You may assume that aluminum chloride is added as a catalyst in each case. For the reactions that will not give a good yield of the desired product, predict the major products. (d) benzamide (PhCONH2) + CH3CH2Cl (Desired Product: p-ethylbenzamide)570views
Textbook QuestionWhich reactions will produce the desired product in good yield? You may assume that aluminum chloride is added as a catalyst in each case. For the reactions that will not give a good yield of the desired product, predict the major products. (e) toluene + HNO3, H2SO4, heat (Desired Product: 2,4,6-trinitrotoluene (TNT))634views
Textbook QuestionPredict the major products formed when benzene reacts (just once) with the following reagents. (h) benzoyl chloride + AlCl3639views
Textbook QuestionPredict the major products formed when benzene reacts (just once) with the following reagents. (e) isobutylene + HF482views
Textbook QuestionPredict the major products of the following reactions. (a) 2,4-dinitrochlorobenzene + NaOCH3 610views
Textbook QuestionPredict the major products of the following reactions. (c) nitrobenzene + fuming sulfuric acid 642views
Textbook Question(••) LOOKING BACK In Chapter 23, we learned about the electrophilic aromatic nitration reaction. When phenol is subjected to these conditions with a large excess of nitric acid, a molecule called picric acid is produced. Predict the product of this reaction and explain why the pKₐ value of this compound is 0.38.<IMAGE>291views
Textbook QuestionPredict the major products of the following reactions.(b) phenol + tert-butyl chloride + AlCl3624views
Textbook Questionb. Rank the same compounds from greatest tendency to least tendency to undergo electrophilic aromatic substitution.259views
Textbook QuestionRank each group of compounds from most reactive to least reactive toward electrophilic aromatic substitution:a. benzene, ethylbenzene, chlorobenzene, nitrobenzene, anisole205views
Textbook QuestionFor each horizontal row of substituted benzenes, indicatec. the one that yields the highest percentage of meta product in an electrophilic aromatic substitution reaction.<IMAGE>180views
Textbook QuestionFor each horizontal row of substituted benzenes, indicatec. the one that yields the highest percentage of meta product in an electrophilic aromatic substitution reaction.<IMAGE>128views
Textbook QuestionAre the following substituents ortho–para directors or meta directors?a. CH=CHC≡N b. NO2 c. CH2OH178views
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