What is the mechanism that leads to the circled, minor product? Is a hydrogen from one of the "branching methyl"s utilized? 10.32 We begin by analyzing the reagent. Water is both a weak nucleophile and a weak base. Next, we look at the substrate uktertiary. When a tertiary substrate is treated with a reagent that is both a weak nucleophile and a weak base, we expect Sl and El proIn a situation like this, it is often difficult to predict whether substitution or elimination will predominate, although the trisubstituted at(which is likely the major product) will certainly be favored over the monosubstituted alkene.H20HO.Major productsMinor product

The alkyl halides are known for the direct bonding of the halogen to the carbon of the hydrocarbon.…

Answered: What is the mechanism that leads to the…

What is the mechanism that leads to the circled, minor product? Is a hydrogen from one of the "branching methyl"s utilized?

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter15: Radical Reactions

Section: Chapter Questions

Problem 12E

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Question

What is the mechanism that leads to the circled, minor product? Is a hydrogen from one of the "branching methyl"s utilized?

10.32 We begin by analyzing the reagent. Water is both a weak nucleophile and a weak base. Next, we look at the substrate uk
tertiary. When a tertiary substrate is treated with a reagent that is both a weak nucleophile and a weak base, we expect Sl and El pro
In a situation like this, it is often difficult to predict whether substitution or elimination will predominate, although the trisubstituted at
(which is likely the major product) will certainly be favored over the monosubstituted alkene.
H20
HO.
Major products
Minor product

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