Rank group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: :- 1-chloro-2, 4-dinitrobenzene, 2,4-dinitrophenol, 1-methyl-2,4-dinitrobenzene
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Q: Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the…
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Rank group of compounds from most reactive to least reactive toward electrophilic
:- 1-chloro-2, 4-dinitrobenzene, 2,4-dinitrophenol, 1-methyl-2,4-dinitrobenzene
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- Rank group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: toluene, p-cresol, benzene, p-xyleneRank group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: :- bromobenzene, chlorobenzene, fluorobenzene, iodobenzeneRank group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: :- p-methylnitrobenzene, 2-chloro-1-methyl-4-nitrobenzene, 1-methyl-2,4-dinitrobenzene, p-chloromethylbenzene
- Rank each group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: a. benzene, ethylbenzene, chlorobenzene, nitrobenzene, anisole b. 1-chloro-2,4-dinitrobenzene, 2,4-dinitrophenol, 1-methyl-2,4-dinitrobenzene c. toluene, p-cresol, benzene, p-xylene d. benzene, benzoic acid, phenol, propylbenzene e. p-methylnitrobenzene, 2-chloro-1-methyl-4-nitrobenzene, 1-methyl-2,4-dinitrobenzene, p-chloromethylbenzene f. bromobenzene, chlorobenzene, fluorobenzene, iodobenzeneRank group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: :- benzene, ethylbenzene, chlorobenzene, nitrobenzene, anisoleRank group of compounds from most reactive to least reactive toward electrophilic aromatic substitution: :- benzene, benzoic acid, phenol, propylbenzene
- Rank the following groups in order of their ability to activate an aromatic compound to electrophilic aromatic substitution.For following substituted benzenes: [1] C6H5Br; [2] C6H5CN; [3] C6H5OCOCH3: Does the substituent activate or deactivate the benzene ring inelectrophilic aromatic substitution?Consider the tetracyclic aromatic compound drawn below, with rings labeled as A, B, C, and (a) Which of the four rings is most reactive in electrophilic aromatic substitution? (b) Which of the four rings is least reactive in electrophilic aromatic substitution? (c) What are the major produces) formed when this compound is treated with one equivalent of Br2?
- Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents.(a) HNO3, H2SO4 (b) Br2, FeBr3 (c) CH3CH2COCl, AlCl3Rank the following aromatic compounds in increasing order of reactivity toward Br2 (least reactive to most reactive) under bromination conditions: Br2, FeBr3.Which of the following substituents are meta directing in electrophilic aromatic substitution? A. CO2H, NO2, CF3 B. OEt, COCH3, Br C. NH2, Me, CCl3 D. F, CF3, OC(O)CH3