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enzoate. The nitro substituent was introduced in the meta position of the methy Why does it preferentially occur at meta, other than para or ortho? Show structures to prove your reasoning. (Be aware that it preferentially goes to meta, which means that the other reactions are not totally excluded.)

enzoate. The nitro substituent was introduced in the meta position of the methy Why does it preferentially occur at meta, other than para or ortho? Show structures to prove your reasoning. (Be aware that it preferentially goes to meta, which means that the other reactions are not totally excluded.)

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
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4. The nitro substituent was introduced in the meta position of the methyl benzoate. Why does it preferentially occur at meta, other than para or ortho? Show structures to prove your reasoning. (Be aware that it preferentially goes to meta, which means that the other reactions are not totally excluded.) covery for today's reaction. (Hint: To deter-
Transcribed Image Text:4. The nitro substituent was introduced in the meta position of the methyl benzoate. Why does it preferentially occur at meta, other than para or ortho? Show structures to prove your reasoning. (Be aware that it preferentially goes to meta, which means that the other reactions are not totally excluded.) covery for today's reaction. (Hint: To deter-
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It is due to the -R effect of the COCH3 gruop, a positive charge will be generated at the ortho- and and para - positions of methyl benzoate.

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