EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
8th Edition
ISBN: 8220102744127
Author: Bruice
Publisher: PEARSON
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Chapter 11.4, Problem 16P
Interpretation Introduction

Interpretation:

The product of the stille reaction should be determined for the given reaction.

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Draw the structure of the alkyl bromide and the nucleophile that will react in an Sy2 reaction to give the product shown. CN Alkyl bromide + Nucleophile H3C • You do not have to consider stereochemistry. Separate multiple reactants using the + sign from the drop-down menu.
Zaitsev's rule for the acid catalyzed dehydration of alcohols states: It states that in a regioselective E1 or E2 reaction the major product is the least stable alkene, i.e., the alkene with the less substituted double bond. O 1) True O 2) False
Do hydration reactions like this one have Markovnikov and anti-Markovnikov products? I know that for addition of halides on alkene double bonds, there are Markovnikov products becasue of 1,2-halide/methyl shifts, but there usually aren't shifts in hydration reactions.  Essentially, would the Markovnikov/major product for this reaction have a hydroxy group attached to the tertiary carbocation and the anti-Markovnikov/minor product for this reaction have a hydroxy group attached to the adjacent secondary carbocation?

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EBK ORGANIC CHEMISTRY

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