Dr. Wolf's CHM 201 & 202 20-1 Ester Hydrolysis in Base: Saponification.
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Transcript of Dr. Wolf's CHM 201 & 202 20-1 Ester Hydrolysis in Base: Saponification.
![Page 1: Dr. Wolf's CHM 201 & 202 20-1 Ester Hydrolysis in Base: Saponification.](https://reader035.fdocuments.us/reader035/viewer/2022071808/56649edb5503460f94beba8b/html5/thumbnails/1.jpg)
Dr. Wolf's CHM 201 & 202 20-1
Ester Hydrolysis in Base:Saponification
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20-2
is called saponification
is irreversible, because of strong stabilization of carboxylate
ion
if carboxylic acid is desired product, saponification is followed
by a separate acidification step (simply a pH adjustment)
Ester Hydrolysis in Aqueous Base
RCO–
O
+ R'OHRCOR'
O
+ HO–
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20-3
Soap-Making
R2COCH
CH2OCR1O
CH2OCR3
O
O
Basic hydrolysis
of the glyceryl
triesters (from
fats and oils)
gives salts of
long-chain
carboxylic acids.
These salts are
soaps.
NaOH , H2O, heat
R1CONa
O
R2CONa
O
R3CONa
O
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20-4
Which bond is broken when esters arehydrolyzed in base?
+••
–OH••••
RC
O
OR'••
••
••••
+ OR'–
••••
••
nucleophilic acyl substitution.
RC
O••••
••
••OH
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Dr. Wolf's CHM 201 & 202 20-5
Stereochemistry gives the same answer
alcohol has same
configuration at
chirality center as
ester; therefore,
nucleophilic acyl
substitution
CH3CONa
O
+
CH3C
O
CO
HC6H5
CH3
C
HO
HC6H5
CH3
NaOH, H2O
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20-6
Involves two stages:
1) formation of tetrahedral intermediate
2) dissociation of tetrahedral
intermediate
Mechanism of Ester Hydrolysisin Base
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20-7
First stage: formation of tetrahedral intermediateFirst stage: formation of tetrahedral intermediate
RC
OH
OH
OR'
+ H2ORCOR'
O
water adds to the
carbonyl group of the
ester
this stage is
analogous to the
base-catalyzed
addition of water to a
ketone
HO–
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Mechanism of formationof
tetrahedral intermediate
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Step 1Step 1
RC
O
OR'
•• ••
••••
RC
O
OR'
••••
••••
O ••
H••
–
••
O ••
H••
•• –
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Step 2Step 2
RC
O
OR'
••••
••••
O ••
H••
–
••
••••
HO
H
RC
O
OR'
••
••••
O ••
H••
••
H
••–••
••O
H
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Dr. Wolf's CHM 201 & 202
Dissociation oftetrahedral intermediate
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Step 3Step 3
RC
O
OR'
••
••••
O ••
H••
••
H
••–••
••O
H
••••
HO
H
OR'••••
– ••
RC
••
O•• ••
••O H
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Step 4Step 4
OR'••••
– ••
RC
••
O•• ••
••O H
HO–
RC
••
O•• ••
••O ••
–
H OR'••
••
H2O
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Nucleophilic addition of hydroxide ion to carbonylgroup in first step
Tetrahedral intermediate formed in first stage
Hydroxide-induced dissociation of tetrahedralintermediate in second stage
Key Features of Mechanism