For the Electrophilic Aromatic Substitution lab you performed an iodination reaction on salicylamide to illustrate directing effects of substituents. What is the directing effects of the substituents of your starting compound that resulted in the placement of the lodo group ? O -(C-OJNH, is an electron withdrawing group and -OH is an electron donating group. lodination will happen meta to the -OH group as the major product. O -(C=O)NH2 is an electron withdrawing group and -OH is an electron donating group. lodination will happen meta to the -(C=O)NH2 group as the major product. O -(C=O)NH2 is an electron withdrawing group and -OH is an electron donating group. lodination will happen para to the -(C-O)NH2 group as the major product. O (C=O)NH2 is an electron withdrawing group and -OH is an electron donating group. lodination will happen para to the -OH group as the major product.

For the Electrophilic Aromatic Substitution lab you performed an iodination reaction on salicylamide to illustrate directing effects of substituents. What is the directing effects of the substituents of your starting compound that resulted in the placement of the lodo group ? O -(C-OJNH, is an electron withdrawing group and -OH is an electron donating group. lodination will happen meta to the -OH group as the major product. O -(C=O)NH2 is an electron withdrawing group and -OH is an electron donating group. lodination will happen meta to the -(C=O)NH2 group as the major product. O -(C=O)NH2 is an electron withdrawing group and -OH is an electron donating group. lodination will happen para to the -(C-O)NH2 group as the major product. O (C=O)NH2 is an electron withdrawing group and -OH is an electron donating group. lodination will happen para to the -OH group as the major product.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 21E

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