1. A. Use curved arrows to illustrate the movement of electrons and any intermediates associated withthe mononitration of resorcinol by nitric acid. Are the OH groups activating or deactivating?B. Draw the expected predominant Friedel-Crafts alkylation product resulting from reaction of tert-butylbromide with meta-xylene, in the presence of AIBR3 (reactants shown below)CH3CH3CH3H3CCH3Br+->C. Use curved arrows to illustrate the movement of electrons and any intermediates associated withthe reaction between xylene and tert-butyl bromideС.

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1. A. Use curved arrows to illustrate the movement of electrons and any intermediates associated with the mononitration of resorcinol by nitric acid. Are the OH groups activating or deactivating?

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 22CTQ

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Question

100%

1. A. Use curved arrows to illustrate the movement of electrons and any intermediates associated with
the mononitration of resorcinol by nitric acid. Are the OH groups activating or deactivating?
B. Draw the expected predominant Friedel-Crafts alkylation product resulting from reaction of tert-butyl
bromide with meta-xylene, in the presence of AIBR3 (reactants shown below)
CH3
CH3
CH3
H3C
CH3
Br
+
->
C. Use curved arrows to illustrate the movement of electrons and any intermediates associated with
the reaction between xylene and tert-butyl bromide
С.

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