OH is a very poor leaving group. However, many alcohols react with alkyl or aryl sulfo- nyl chlorides to give sulfonate esters. R-OH + R'- C - R,N >R-O-S-R' + HCI Suggest the product of the following reaction. CH,CH,-0-S-C,H; + CH,S¯N * DMSO
OH is a very poor leaving group. However, many alcohols react with alkyl or aryl sulfo- nyl chlorides to give sulfonate esters. R-OH + R'- C - R,N >R-O-S-R' + HCI Suggest the product of the following reaction. CH,CH,-0-S-C,H; + CH,S¯N * DMSO
Chapter17: Alcohols And Phenols
Section17.SE: Something Extra
Problem 69AP: As a rule, axial alcohols oxidize somewhat faster than equatorial alcohols. Which would you expect...
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![OH is a very poor leaving group. However, many alcohols react with alkyl or aryl sulfo-
nyl chlorides to give sulfonate esters.
R-OH + R'-
C -
R,N
>R-O-S-R' + HCI](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F53757b5e-ea5c-448a-ad88-92493887cbb9%2F3710cb02-d240-413a-9c94-68767b4f0945%2Fo7ceczk.jpeg&w=3840&q=75)
Transcribed Image Text:OH is a very poor leaving group. However, many alcohols react with alkyl or aryl sulfo-
nyl chlorides to give sulfonate esters.
R-OH + R'-
C -
R,N
>R-O-S-R' + HCI
![Suggest the product of the following reaction.
CH,CH,-0-S-C,H; + CH,S¯N *
DMSO](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F53757b5e-ea5c-448a-ad88-92493887cbb9%2F3710cb02-d240-413a-9c94-68767b4f0945%2Fdrqac0p.jpeg&w=3840&q=75)
Transcribed Image Text:Suggest the product of the following reaction.
CH,CH,-0-S-C,H; + CH,S¯N *
DMSO
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