2) Show the two competing reaction mechanisms (SN1 and SN2) for the following reaction. OH + S-OH Bu N CI A sulfonic acid: pKa - 0 The mechanism starts with an acid base reaction mediated by a sulfonic acid (RSO 3H, pKa 0). Does this reagent act as a catalyst? Please explain. In addition, draw the reaction energy diagrams for both reaction mechanisms. Show activation energies, transition states, and the free energy of the reaction (delta G).

Chemistry & Chemical Reactivity
9th Edition
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Chapter14: Chemical Kinetics: The Rates Of Chemical Reactions
Section: Chapter Questions
Problem 86IL: The acid-catalyzed iodination of acetone CH3COCH3(aq) + I2(aq) CH3COCH2I(aq) + HI(aq) is a common...
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2) Show the two competing reaction mechanisms (SN1 and SN2) for the following reaction.
OH
+
S-OH Bu N
CI
A sulfonic acid: pKa - 0
The mechanism starts with an acid base reaction mediated by a sulfonic acid (RSO 3H,
pKa 0). Does this reagent act as a catalyst? Please explain.
In addition, draw the reaction energy diagrams for both reaction mechanisms. Show
activation energies, transition states, and the free energy of the reaction (delta G).
Transcribed Image Text:2) Show the two competing reaction mechanisms (SN1 and SN2) for the following reaction. OH + S-OH Bu N CI A sulfonic acid: pKa - 0 The mechanism starts with an acid base reaction mediated by a sulfonic acid (RSO 3H, pKa 0). Does this reagent act as a catalyst? Please explain. In addition, draw the reaction energy diagrams for both reaction mechanisms. Show activation energies, transition states, and the free energy of the reaction (delta G).
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