The following reaction follows the kinetics SN1 The substrate is: - Water - the cyanide ion - 1-ethylbenzene bromide. - 3-phenylpropanenitrile CH₂CH₂Br CN H₂O OCN Since the following reaction follows an SN1 mechanism, it is correct to state: CH₂CH₂Br CH₂CH₂CN -Favors the formation of two products. -The transition state involves a pentavalent carbon. -The reaction occurs in a single step. - The first step of the reaction involves the formation of a carbocation. H₂O CH₂CH₂CN

The following reaction follows the kinetics SN1 The substrate is: - Water - the cyanide ion - 1-ethylbenzene bromide. - 3-phenylpropanenitrile CH₂CH₂Br CN H₂O OCN Since the following reaction follows an SN1 mechanism, it is correct to state: CH₂CH₂Br CH₂CH₂CN -Favors the formation of two products. -The transition state involves a pentavalent carbon. -The reaction occurs in a single step. - The first step of the reaction involves the formation of a carbocation. H₂O CH₂CH₂CN

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions

Section19.SE: Something Extra

Problem 28VC

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