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

Chemistry
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Chapter1: Chemical Foundations
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The following reaction follows the kinetics SN1
The substrate is:
- Water
- the cyanide ion
- 1-ethylbenzene bromide.
- 3-phenylpropanenitrile
CH₂CH₂Br
CN
H₂O
CN
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
Transcribed Image Text:The following reaction follows the kinetics SN1 The substrate is: - Water - the cyanide ion - 1-ethylbenzene bromide. - 3-phenylpropanenitrile CH₂CH₂Br CN H₂O CN 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
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