4. Consider the following reaction. This reaction is a multi-step reaction. [1] Draw the mechanism for each step of this reaction using curved arrow notation, include all lone pairs of electrons if they are directly involved in the reaction. protected and may nshared, addist [2] Identify the arrow pushing pattern (mechanistic pattern: nucleophilic attack, loss of leaving group, or proton transfer) for each step. [3] Draw a transition state for each step. d H-OSO3H ~ -OSO3H CH3 90 H | Хо-сна H3C-O-H → O-H H3C-O-H

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter8: Addition Via Carbocation
Section: Chapter Questions
Problem 4E: Draw the complete mechanism of each pair of reactants including any favorable rearrangements and all...
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4. Consider the following reaction. This reaction is a multi-step reaction.
[1] Draw the mechanism for each step of this reaction using curved arrow notation, include all lone
pairs of electrons if they are directly involved in the reaction.
[2] Identify the arrow pushing pattern (mechanistic pattern: nucleophilic attack, loss of leaving
group, or proton transfer) for each step.
[3] Draw a transition state for each step.
H-OSO3H
CH3
00
H
H3C-O-H
Хосно
H3C-O-H
H
Transcribed Image Text:This content is protected and may nag shared t 4. Consider the following reaction. This reaction is a multi-step reaction. [1] Draw the mechanism for each step of this reaction using curved arrow notation, include all lone pairs of electrons if they are directly involved in the reaction. [2] Identify the arrow pushing pattern (mechanistic pattern: nucleophilic attack, loss of leaving group, or proton transfer) for each step. [3] Draw a transition state for each step. H-OSO3H CH3 00 H H3C-O-H Хосно H3C-O-H H
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