Shown below is the complete mechanism for an SN1 reaction: potential energy H₂C -[-DJ-CHI] H₂C intermediate H₂C S1 mechanism rate ΔΗ CH, H,C intermediate The accompanying activation energy diagram is: endothermic H₂C- transition state H₂C transition state transition state M determining E step intermediate CH, H,C transition state AH H.... exothermic reaction coordinate 8+ H transition state intermediate AH exothermic H₂C SÖH Н H₂C products Select all statements below that are true. Points will be deducted for incorrect choices. H₂C CH, H₂C transition state The higher energy intermediate is the carbocation. Oxonium (oxygen with a +1 formal charge and three bonds) is one of two intermediates formed. Water is the electrophile. The 3rd transition state shows proton transfer. Chlorine is the nucleophile. The 1st transition state involves a leaving group leaving. The reaction would be faster if fluorine was used in place of chlorine. H 10 H
Shown below is the complete mechanism for an SN1 reaction: potential energy H₂C -[-DJ-CHI] H₂C intermediate H₂C S1 mechanism rate ΔΗ CH, H,C intermediate The accompanying activation energy diagram is: endothermic H₂C- transition state H₂C transition state transition state M determining E step intermediate CH, H,C transition state AH H.... exothermic reaction coordinate 8+ H transition state intermediate AH exothermic H₂C SÖH Н H₂C products Select all statements below that are true. Points will be deducted for incorrect choices. H₂C CH, H₂C transition state The higher energy intermediate is the carbocation. Oxonium (oxygen with a +1 formal charge and three bonds) is one of two intermediates formed. Water is the electrophile. The 3rd transition state shows proton transfer. Chlorine is the nucleophile. The 1st transition state involves a leaving group leaving. The reaction would be faster if fluorine was used in place of chlorine. H 10 H
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...
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do both with detail mechanism explanation plz if u plan to do only 1 then skip do both
![Shown below is the complete mechanism for an SN1 reaction:
potential energy
H₂C
-[-DJ-CHI]
H₂C
intermediate
H₂C
S1 mechanism
rate
ΔΗ
CH,
H,C
intermediate
The accompanying activation energy diagram is:
endothermic
H₂C-
transition state
H₂C
transition state
transition state
M
determining E
step
intermediate
CH,
H,C
transition state
AH
H....
exothermic
reaction coordinate
8+
H
transition state
intermediate
AH
exothermic
H₂C
SÖH
Н
H₂C
products
Select all statements below that are true. Points will be deducted for incorrect choices.
H₂C
CH,
H₂C
transition state
The higher energy intermediate is the carbocation.
Oxonium (oxygen with a +1 formal charge and three bonds) is one of two intermediates formed.
Water is the electrophile.
The 3rd transition state shows proton transfer.
Chlorine is the nucleophile.
The 1st transition state involves a leaving group leaving.
The reaction would be faster if fluorine was used in place of chlorine.
H
10
H](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F9fc8803e-b5ce-4a0a-ad9a-c206d0584d33%2F016afb98-3de3-43ea-baf2-1bba6667f6ce%2F36hg8w8_processed.png&w=3840&q=75)
Transcribed Image Text:Shown below is the complete mechanism for an SN1 reaction:
potential energy
H₂C
-[-DJ-CHI]
H₂C
intermediate
H₂C
S1 mechanism
rate
ΔΗ
CH,
H,C
intermediate
The accompanying activation energy diagram is:
endothermic
H₂C-
transition state
H₂C
transition state
transition state
M
determining E
step
intermediate
CH,
H,C
transition state
AH
H....
exothermic
reaction coordinate
8+
H
transition state
intermediate
AH
exothermic
H₂C
SÖH
Н
H₂C
products
Select all statements below that are true. Points will be deducted for incorrect choices.
H₂C
CH,
H₂C
transition state
The higher energy intermediate is the carbocation.
Oxonium (oxygen with a +1 formal charge and three bonds) is one of two intermediates formed.
Water is the electrophile.
The 3rd transition state shows proton transfer.
Chlorine is the nucleophile.
The 1st transition state involves a leaving group leaving.
The reaction would be faster if fluorine was used in place of chlorine.
H
10
H
Transcribed Image Text:Predict the major product formed in the following reaction.
Compound 1
O Compound 2
O Compound 3
O Compound 4
1)
3)
Br
NaSCH3
SH
2)
Major product
SH
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