ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
12th Edition
ISBN: 9781119304241
Author: Solomons
Publisher: WILEY C
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Chapter 13, Problem 2PP
Interpretation Introduction

Interpretation:

The resonance structures for the carbocation formed by (E)2butenyltrifluoromethanesulfonate are to be drawn and the resonance structure that contribute greater to the hybrid is to be determined. Also the products formed by the reaction of carbocation with a chloride ion are to be determined.

Concept introduction:

Secondary and tertiary carbocations are more stable than a primary carbocation.

Resonance is defined as the movement of pi-electrons from one carbon to another in order to stabilize the charged intermediates.

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A pdf file of your hand drawn, stepwise mechanisms for the reactions. For each reaction in the assignment, you must write each mechanism three times (there are 10 reactions, so 30 mechanisms). (A) do the work on a tablet and save as a pdf., it is expected to write each mechanism out and NOT copy and paste the mechanism after writing it just once. Everything should be drawn out stepwise  and  every bond that is formed and broken in the process of the reaction, and is expected to see all relevant lone pair electrons and curved arrows.
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Chapter 13 Solutions

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS

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