7.13 Chemical Reactions That Produce Diastereomers.
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Transcript of 7.13 Chemical Reactions That Produce Diastereomers.
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7.13 7.13
Chemical Reactions That Chemical Reactions That
Produce Diastereomers Produce Diastereomers
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In order to know understand stereochemistry of In order to know understand stereochemistry of product, you need to know two things:product, you need to know two things:
(1) stereochemistry of alkene (cis or trans; (1) stereochemistry of alkene (cis or trans; Z or E) Z or E)(2) stereochemistry of mechanism (syn or anti)(2) stereochemistry of mechanism (syn or anti)
Stereochemistry of Addition to AlkenesStereochemistry of Addition to Alkenes
CC CC ++ E—YE—Y CC CCEE YY
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BrBr22
RR
SS RR
SS
mesomeso
anti addition to anti addition to transtrans-2-butene gives meso -2-butene gives meso diastereomerdiastereomer
Bromine Addition to trans-2-ButeneBromine Addition to trans-2-ButeneFig. 7.14 (p 284)Fig. 7.14 (p 284)
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BrBr22
RR
RR SS
SS
50%50% 50%50%
Bromine Addition to cis-2-ButeneBromine Addition to cis-2-ButeneFig. 7.15 (p 285)Fig. 7.15 (p 285)
anti addition to anti addition to ciscis-2-butene gives racemic -2-butene gives racemic mixture of chiral diastereomermixture of chiral diastereomer
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RCORCO33HH
RR
RR SS
SS
syn addition to syn addition to transtrans-2-butene gives racemic -2-butene gives racemic mixture of chiral diastereomermixture of chiral diastereomer
Epoxidation of trans-2-ButeneEpoxidation of trans-2-ButeneProblem 7.17 (p 285)Problem 7.17 (p 285)
50%50% 50%50%
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RR
SS RR
SS
Epoxidation of cis-2-ButeneEpoxidation of cis-2-ButeneProblem 7.17 (p 285)Problem 7.17 (p 285)
syn addition to syn addition to ciscis-2-butene gives meso -2-butene gives meso diastereomerdiastereomer
RCORCO33HH
mesomeso
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of two stereoisomers of a particular starting of two stereoisomers of a particular starting material, each one gives differentmaterial, each one gives differentstereoisomeric forms of the productstereoisomeric forms of the product
related to mechanism: terms such asrelated to mechanism: terms such assyn addition and anti addition refer tosyn addition and anti addition refer tostereospecificitystereospecificity
Stereospecific reactionStereospecific reaction
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..
transtrans-2-butene-2-butene
ciscis-2-butene-2-butene
transtrans-2-butene-2-butene
ciscis-2-butene-2-butene brominationbromination antianti 22RR,3,3RR + 2 + 2SS,3,3SS
brominationbromination
epoxidationepoxidation
epoxidationepoxidation
antianti
synsyn
synsyn
mesomeso
mesomeso
22RR,3,3RR + 2 + 2SS,3,3SS
Stereospecific reactionStereospecific reaction
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a single starting material can give two or morea single starting material can give two or morestereoisomeric products, but gives one of themstereoisomeric products, but gives one of themin greater amounts than any otherin greater amounts than any other
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CHCH33
HH
CHCH33
HH
68%68% 32%32%
Stereoselective reactionStereoselective reaction
CHCH33
CHCH22
HH
CHCH33
HH
CHCH33
HH
HH22
PtPt
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7.14 7.14
Resolution of EnantiomersResolution of Enantiomers
separation of a racemic mixture into its two separation of a racemic mixture into its two enantiomeric formsenantiomeric forms
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enantiomersenantiomers
C(+)C(+)C(+)C(+) C(-)C(-)C(-)C(-)
StrategyStrategy
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enantiomersenantiomers
C(+)C(+)C(+)C(+) C(-)C(-)C(-)C(-)
2P(+)2P(+)
C(+)C(+)P(+)C(+)C(+)P(+) C(-)C(-)P(+)C(-)C(-)P(+)
diastereomersdiastereomers
StrategyStrategy
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enantiomersenantiomers
C(+)C(+)C(+)C(+) C(-)C(-)C(-)C(-)
2P(+)2P(+)
C(+)C(+)P(+)C(+)C(+)P(+) C(-)C(-)P(+)C(-)C(-)P(+)
diastereomersdiastereomers
C(+)C(+)P(+)C(+)C(+)P(+)
C(-)C(-)P(+)C(-)C(-)P(+)
StrategyStrategy
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enantiomersenantiomers
C(+)C(+)C(+)C(+) C(-)C(-)C(-)C(-)
2P(+)2P(+)
C(+)C(+)P(+)C(+)C(+)P(+) C(-)C(-)P(+)C(-)C(-)P(+)
diastereomersdiastereomers
C(+)C(+)P(+)C(+)C(+)P(+)
C(-)C(-)P(+)C(-)C(-)P(+)
P(+)P(+)
P(+)P(+)
C(+)C(+)C(+)C(+)
C(-)C(-)C(-)C(-)
StrategyStrategy
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7.157.15
Stereoregular PolymersStereoregular Polymers
atacticatactic
isotacticisotactic
syndiotacticsyndiotactic
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Atactic PolypropyleneAtactic Polypropylene
random stereochemistry of methyl groups random stereochemistry of methyl groups attached to main chain (stereorandom)attached to main chain (stereorandom)
properties not very useful for fibers etc.properties not very useful for fibers etc.
formed by free-radical polymerizationformed by free-radical polymerization
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Isotactic PolypropyleneIsotactic Polypropylene
stereoregular polymer; all methyl groups onstereoregular polymer; all methyl groups onsame side of main chainsame side of main chain
useful propertiesuseful properties
prepared by coordination polymerization prepared by coordination polymerization under Ziegler-Natta conditionsunder Ziegler-Natta conditions
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Syndiotactic PolypropyleneSyndiotactic Polypropylene
stereoregular polymer; methyl groups stereoregular polymer; methyl groups alternate side-to-side on main chainalternate side-to-side on main chain
useful propertiesuseful properties
prepared by coordination polymerization prepared by coordination polymerization under Ziegler-Natta conditionsunder Ziegler-Natta conditions
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7.167.16
Stereogenic CentersStereogenic Centers
Other Than CarbonOther Than Carbon
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SiliconSilicon
silicon, like carbon, forms four bonds in its silicon, like carbon, forms four bonds in its stable compounds and many chiral silicon stable compounds and many chiral silicon compounds have been resolvedcompounds have been resolved
SiSi SiSidd dd
aabb
cc
aabb
cc
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Nitrogen in aminesNitrogen in amines
pyramidal geometry at nitrogen can produce a pyramidal geometry at nitrogen can produce a chiral structure, but enantiomers equilibrate chiral structure, but enantiomers equilibrate too rapidly to be resolvedtoo rapidly to be resolved
NN NN:: ::
aabb
cc
aabb
cc
very fastvery fast
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Phosphorus in phosphinesPhosphorus in phosphines
pyramidal geometry at phosphorus can pyramidal geometry at phosphorus can produce a chiral structure; pyramidal produce a chiral structure; pyramidal inversion slower than for amines and inversion slower than for amines and compounds of the type shown have been compounds of the type shown have been resolvedresolved
PP PP:: ::
aabb
cc
aabb
cc
slowslow
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Sulfur in sulfoxidesSulfur in sulfoxides
pyramidal geometry at sulfur can produce a pyramidal geometry at sulfur can produce a chiral structure; pyramidal inversion is slow chiral structure; pyramidal inversion is slow and compounds of the type shown have been and compounds of the type shown have been resolvedresolved
SS SS:: ::
aabb
O_O_
aabb
O_O_
slowslow
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