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16.46 Rank the following compounds in order of increasing reactivity in electrophilic bromination. In each case, indi- cate whether the principal monobromination products will be the ortho and para isomers or the meta isomer, and whether the compound will be more or less reactive than benzene. Explain carefully the points that cause any uncertainty. -N(CH3)3 deact CH,N(CH3)3 A meta B N(CH3), CH3 IS.

16.46 Rank the following compounds in order of increasing reactivity in electrophilic bromination. In each case, indi- cate whether the principal monobromination products will be the ortho and para isomers or the meta isomer, and whether the compound will be more or less reactive than benzene. Explain carefully the points that cause any uncertainty. -N(CH3)3 deact CH,N(CH3)3 A meta B N(CH3), CH3 IS.

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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s on 16.46 Rank the following compounds in order of increasing reactivity in electrophilic bromination. In each case, indi- cate whether the principal monobromination products will be the ortho and para isomers or the meta isomer, and whether the compound will be more or less reactive than benzene. Explain carefully the points that cause any uncertainty. the ху- the nan -CH,N(CH,), N(CH3)3 deact A meta В ng agents. N(CH,), CH3 act act ol P D
Transcribed Image Text:s on 16.46 Rank the following compounds in order of increasing reactivity in electrophilic bromination. In each case, indi- cate whether the principal monobromination products will be the ortho and para isomers or the meta isomer, and whether the compound will be more or less reactive than benzene. Explain carefully the points that cause any uncertainty. the ху- the nan -CH,N(CH,), N(CH3)3 deact A meta В ng agents. N(CH,), CH3 act act ol P D
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Applying inductive, hyperconjugation & mesomeric effect .

Mesomeric >hyperconjugation> inductive effect

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