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of 8 -+ Automatic Zoomn View as To Which one of the following benzene analogs provides neither ortho nor para product? (a) Acetophenone (b) Toluene (c) Aniline (d) Phenol Predict an increase in the reactivity of various benzene derivatives for the formation of para-produ (1) Anisole, (II) Chloro benzene, (III) N,N-dimethyl Aniline (IV) benzyl alcohol (a) | < ||| < || < IV (b) II < IV <1 < III (c) | < || < III < IV (d) II < ||| < |V < | Which of the following is the strongest deactivating group in electrophilic aromatic substitution reactions? (b) -OCH3 (d) -NO2 (c) -CO₂CH3 (a) -CH₂CH3 (e) -N(CH3)2 Circle the benzene analog that undergoes Friedel-Crafts alkylation/acylation most rapidly? CF3 OMe COOH CN 8

of 8 -+ Automatic Zoomn View as To Which one of the following benzene analogs provides neither ortho nor para product? (a) Acetophenone (b) Toluene (c) Aniline (d) Phenol Predict an increase in the reactivity of various benzene derivatives for the formation of para-produ (1) Anisole, (II) Chloro benzene, (III) N,N-dimethyl Aniline (IV) benzyl alcohol (a) | < ||| < || < IV (b) II < IV <1 < III (c) | < || < III < IV (d) II < ||| < |V < | Which of the following is the strongest deactivating group in electrophilic aromatic substitution reactions? (b) -OCH3 (d) -NO2 (c) -CO₂CH3 (a) -CH₂CH3 (e) -N(CH3)2 Circle the benzene analog that undergoes Friedel-Crafts alkylation/acylation most rapidly? CF3 OMe COOH CN 8

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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1 of 8 +Autornatic Zoom View as T 1) Which one of the following benzene analogs provides neither ortho nor para product? (a) Acetophenone (b) Toluene (c) Aniline 4 (d) Phenol 2) Predict an increase in the reactivity of various benzene derivatives for the formation of para-produ (1) Anisole, (II) Chloro benzene, (III) N,N-dimethyl Aniline (IV) benzyl alcohol (a) | < || < || < |V (b) II < IV < | < ||| (c) | < || < III < IV (d) || < ||| < IV < I 3) Which of the following is the strongest deactivating group in electrophilic aromatic substitution reactions? (c) -CO₂CH3 (b) -OCH3 (d) -NO2 (e) -N(CH3)2 (a) -CH₂CH3 4) Circle the benzene analog that undergoes Friedel-Crafts alkylation/acylation most rapidly? OMe CF3 COOH 18 8 [ 15
Transcribed Image Text:1 of 8 +Autornatic Zoom View as T 1) Which one of the following benzene analogs provides neither ortho nor para product? (a) Acetophenone (b) Toluene (c) Aniline 4 (d) Phenol 2) Predict an increase in the reactivity of various benzene derivatives for the formation of para-produ (1) Anisole, (II) Chloro benzene, (III) N,N-dimethyl Aniline (IV) benzyl alcohol (a) | < || < || < |V (b) II < IV < | < ||| (c) | < || < III < IV (d) || < ||| < IV < I 3) Which of the following is the strongest deactivating group in electrophilic aromatic substitution reactions? (c) -CO₂CH3 (b) -OCH3 (d) -NO2 (e) -N(CH3)2 (a) -CH₂CH3 4) Circle the benzene analog that undergoes Friedel-Crafts alkylation/acylation most rapidly? OMe CF3 COOH 18 8 [ 15
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