This question has TWO parts. Provide your answers to the following questions. Indicate your answers clearly. From the following reaction, Problem viewing the image. Click Preview Here 2.1) Draw the the step-by-step curved arrow pushing mechanism to show the formation of the carbocation electrophile starting from the reaction between the alkene and acid (H-CI) given to you below. H-CI: Problem viewing the image, Click Preview Here HCI (cat.) 2.1) Draw the the step-by-step curved arrow pushing mechanism to show the formation of the carbocation electrophile starting from the reaction between the alkene and acid (H-CI) given to you below. x H-CI: Problem viewing the image, Click Preview Here 2.2) Draw the step-by-step curved arrow pushing Electrophilic Aromatic Substitution mechanism to show the formation of the major organic final product starting from the reaction between benzene and the specific carbocation electrophile from Question 2.1. Use Cl as the base in the last proton transfer step. Lone pair electrons and ALL related resonance contributors of the sigma complex must be included in your drawing.

This question has TWO parts. Provide your answers to the following questions. Indicate your answers clearly. From the following reaction, Problem viewing the image. Click Preview Here 2.1) Draw the the step-by-step curved arrow pushing mechanism to show the formation of the carbocation electrophile starting from the reaction between the alkene and acid (H-CI) given to you below. H-CI: Problem viewing the image, Click Preview Here HCI (cat.) 2.1) Draw the the step-by-step curved arrow pushing mechanism to show the formation of the carbocation electrophile starting from the reaction between the alkene and acid (H-CI) given to you below. x H-CI: Problem viewing the image, Click Preview Here 2.2) Draw the step-by-step curved arrow pushing Electrophilic Aromatic Substitution mechanism to show the formation of the major organic final product starting from the reaction between benzene and the specific carbocation electrophile from Question 2.1. Use Cl as the base in the last proton transfer step. Lone pair electrons and ALL related resonance contributors of the sigma complex must be included in your drawing.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter21: Nas: Nucleophilic Aromatic Substitution

Section: Chapter Questions

Problem 6E

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