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11.) Answer true or false for the following questions. Write your answers next to each question. 1) Benzene undergoes electrophilic aromatic substitution reactions with reactive electrophiles. 2) The electrophilic aromatic substitution reaction mechanism involves an initial loss of aromaticity. 3) Meta substitution means a 1,3 arrangement on a benzene ring.

11.) Answer true or false for the following questions. Write your answers next to each question. 1) Benzene undergoes electrophilic aromatic substitution reactions with reactive electrophiles. 2) The electrophilic aromatic substitution reaction mechanism involves an initial loss of aromaticity. 3) Meta substitution means a 1,3 arrangement on a benzene ring.

Chemistry
Chemistry
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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
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11.) Answer true or false for the following questions. Write your answers next to each question. 1) Benzene undergoes electrophilic aromatic substitution reactions with reactive electrophiles. 2) The electrophilic aromatic substitution reaction mechanism involves an initial loss of aromaticity. 3) Meta substitution means a 1,3 arrangement on a benzene ring. 4) The rate determining step in an electrophilic aromatic substitution is the formation of a resonance stabilized radical. 5) Phenols are formed via oxidation of quinones. 6) Birch reduction reaction conditions involve sodium metal, in an alcoholic solution of ammonia. 7) Benzyne is 6r Hückel aromatic. 8) Chlorine is a meta directing, activating substituent for electrophilic aromatic substitution. 9) Aromatic compounds are more stable than antiaromatic compounds. 10) Cyclopentane has less ring strain than an epoxide. 11) Cyclobutadiene is more stable than butadiene. 12) Kinetic products are always more stable than thermodynamic products. 13) Epoxides are more reactive than normal ethers.
Transcribed Image Text:11.) Answer true or false for the following questions. Write your answers next to each question. 1) Benzene undergoes electrophilic aromatic substitution reactions with reactive electrophiles. 2) The electrophilic aromatic substitution reaction mechanism involves an initial loss of aromaticity. 3) Meta substitution means a 1,3 arrangement on a benzene ring. 4) The rate determining step in an electrophilic aromatic substitution is the formation of a resonance stabilized radical. 5) Phenols are formed via oxidation of quinones. 6) Birch reduction reaction conditions involve sodium metal, in an alcoholic solution of ammonia. 7) Benzyne is 6r Hückel aromatic. 8) Chlorine is a meta directing, activating substituent for electrophilic aromatic substitution. 9) Aromatic compounds are more stable than antiaromatic compounds. 10) Cyclopentane has less ring strain than an epoxide. 11) Cyclobutadiene is more stable than butadiene. 12) Kinetic products are always more stable than thermodynamic products. 13) Epoxides are more reactive than normal ethers.
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