5.1 Alkene Nomenclature
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5.15.1Alkene NomenclatureAlkene Nomenclature
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AlkenesAlkenes
Alkenes are hydrocarbons that contain a Alkenes are hydrocarbons that contain a carbon-carbon double bondcarbon-carbon double bond
also called "olefins"also called "olefins"
characterized by molecular formula Ccharacterized by molecular formula CnnHH2n2n
said to be "unsaturated"said to be "unsaturated"
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HH22CC CHCH22 HH22CC CHCHCHCH33
EtheneEtheneoror
EthyleneEthylene(both are acceptable(both are acceptable
IUPAC names)IUPAC names)
PropenePropene
(Propylene is(Propylene issometimes used sometimes used
but is not an acceptablebut is not an acceptableIUPAC name)IUPAC name)
Alkene NomenclatureAlkene Nomenclature
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1) Find the longest continuous chain that 1) Find the longest continuous chain that includes the double bond.includes the double bond.
2) Replace the -2) Replace the -aneane ending of the unbranched ending of the unbranched alkane having the same number of carbons alkane having the same number of carbons by -by -eneene..
3) Number the chain in the direction that gives 3) Number the chain in the direction that gives the lowest number to the doubly bonded the lowest number to the doubly bonded carbon.carbon.
HH22CC CHCHCHCH22CHCH33
Alkene NomenclatureAlkene Nomenclature
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1) Find the longest continuous chain that 1) Find the longest continuous chain that includes the double bond.includes the double bond.
2) Replace the -2) Replace the -aneane ending of the unbranched ending of the unbranched alkane having the same number of carbons alkane having the same number of carbons by -by -eneene..
3) Number the chain in the direction that gives 3) Number the chain in the direction that gives the lowest number to the doubly bonded the lowest number to the doubly bonded carbon.carbon.
HH22CC CHCHCHCH22CHCH33 1-Butene1-Butene
Alkene NomenclatureAlkene Nomenclature
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4) If a substituent is present, identify its position 4) If a substituent is present, identify its position by number. The double bond takes by number. The double bond takes precedence over alkyl groups and halogens precedence over alkyl groups and halogens when the chain is numbered.when the chain is numbered.The compound shown above isThe compound shown above is4-bromo-3-methyl-1-butene.4-bromo-3-methyl-1-butene.
HH22CC CHCHCHCHCHCH22BrBr
CHCH33
Alkene NomenclatureAlkene Nomenclature
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4) If a substituent is present, identify its position 4) If a substituent is present, identify its position by number. by number. Hydroxyl groups take Hydroxyl groups take precedence over the double bond when the precedence over the double bond when the chain is numbered.chain is numbered.The compound shown above isThe compound shown above is2-methyl-3-buten-1-ol.2-methyl-3-buten-1-ol.
HH22CC CHCHCHCHCHCH22OHOH
CHCH33
Alkene NomenclatureAlkene Nomenclature
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methylenemethylene
vinylvinyl
allylallyl
isopropenylisopropenyl
CHCHHH22CC
HH22CC CHCHCHCH22
HH22CC CCHCCH33
HH22CC
Alkenyl GroupsAlkenyl Groups
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Cycloalkene NomenclatureCycloalkene Nomenclature
1) Replace the -1) Replace the -aneane ending of the cycloalkane ending of the cycloalkane having the same number of carbons by -having the same number of carbons by -eneene..
CyclohexeneCyclohexene
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1) Replace the -1) Replace the -aneane ending of the cycloalkane ending of the cycloalkane having the same number of carbons by -having the same number of carbons by -eneene..
2) Number 2) Number throughthrough the double bond in the the double bond in thedirection that gives the lower number to the direction that gives the lower number to the first-appearing substituent.first-appearing substituent.
Cycloalkene NomenclatureCycloalkene Nomenclature
CHCH33
CHCH22CHCH33
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1) Replace the -1) Replace the -aneane ending of the cycloalkane ending of the cycloalkane having the same number of carbons by -having the same number of carbons by -eneene..
2) Number 2) Number throughthrough the double bond in the the double bond in thedirection that gives the lower number to the direction that gives the lower number to the first-appearing substituent.first-appearing substituent.
6-Ethyl-1-methylcyclohexene6-Ethyl-1-methylcyclohexeneCHCH33
CHCH22CHCH33
Cycloalkene NomenclatureCycloalkene Nomenclature
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5.125.12Structure and Bonding in AlkenesStructure and Bonding in Alkenes
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bond angles: bond angles: H-C-H = 117°H-C-H = 117°
H-C-C = 121°H-C-C = 121°
bond distances: bond distances: C—H = 110 pmC—H = 110 pm
C=C = 134 pmC=C = 134 pm
planarplanar
Structure of EthyleneStructure of Ethylene
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Framework of Framework of bonds bondsEach carbon is Each carbon is spsp22 hybridized hybridized
Bonding in EthyleneBonding in Ethylene
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Each carbon has a half-filled Each carbon has a half-filled pp orbital orbital
Bonding in EthyleneBonding in Ethylene
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Side-by-side overlap of half-Side-by-side overlap of half-filled filled pp orbitals gives a orbitals gives a bond bond
Bonding in EthyleneBonding in Ethylene
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5.35.3Isomerism in AlkenesIsomerism in Alkenes
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Isomers are different compounds thatIsomers are different compounds thathave the same molecular formula.have the same molecular formula.
IsomersIsomers
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Isomers
Constitutional isomers Stereoisomers
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Isomers
Constitutional isomers Stereoisomers
different connectivitydifferent connectivitysame connectivity;same connectivity;
different arrangementdifferent arrangementof atoms in spaceof atoms in space
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Isomers
Constitutional isomers Stereoisomers
consider the isomeric alkenes of consider the isomeric alkenes of molecular formula Cmolecular formula C44HH88
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2-Methylpropene2-Methylpropene1-Butene1-Butene
cis-cis-2-Butene2-Butene trans-trans-2-Butene2-Butene
CC CC
HH
HH HH
CHCH22CHCH33
HH33CC
CC CC
CHCH33
HH
HHHH
CHCH33
CC CC
HH33CC
HH
CC CC
HH
HHHH33CC
HH33CC
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2-Methylpropene2-Methylpropene1-Butene1-Butene
cis-cis-2-Butene2-Butene
CC CC
HH
HH HH
CHCH22CHCH33
HH
CHCH33
CC CC
HH33CC
HH
CC CC
HH
HHHH33CC
HH33CC
Constitutional isomersConstitutional isomers
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2-Methylpropene2-Methylpropene1-Butene1-Butene
trans-trans-2-Butene2-Butene
CC CC
HH
HH HH
CHCH22CHCH33
HH33CC
CC CC
CHCH33
HH
HH
CC CC
HH
HHHH33CC
HH33CC
Constitutional isomersConstitutional isomers
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cis-cis-2-Butene2-Butene trans-trans-2-Butene2-Butene
HH33CC
CC CC
CHCH33
HH
HHHH
CHCH33
CC CC
HH33CC
HH
StereoisomersStereoisomers
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trans (identical or trans (identical or analogous substituents analogous substituents on opposite sides)on opposite sides)
Stereochemical NotationStereochemical Notation
cis (identical or cis (identical or analogous substitutents analogous substitutents on same side)on same side)
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transtransciscis
Interconversion of stereoisomericInterconversion of stereoisomericalkenes does not normally occur.alkenes does not normally occur.
Requires that Requires that component of doublecomponent of doublebond be broken.bond be broken.
Figure 5.2Figure 5.2
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transtransciscis
Figure 5.2Figure 5.2
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5.45.4Naming Steroisomeric AlkenesNaming Steroisomeric Alkenesby the E-Z Notational Systemby the E-Z Notational System
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Stereochemical NotationStereochemical Notation
cis and trans are useful when substituents are cis and trans are useful when substituents are identical or analogous (oleic acid has a cis identical or analogous (oleic acid has a cis double bond)double bond)cis and trans are ambiguous when analogies cis and trans are ambiguous when analogies are not obviousare not obvious
CC CC
CHCH33(CH(CH22))66CHCH22 CHCH22(CH(CH22))66COCO22HH
HH HH
Oleic acidOleic acid
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ExampleExample
What is needed:What is needed:
1) 1) systematic body of rules for ranking systematic body of rules for ranking substituentssubstituents2)2) new set of stereochemical symbols othernew set of stereochemical symbols otherthan cis and transthan cis and trans
CC CC
HH FF
ClCl BrBr
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CC CC
EE : : higher ranked substituents on higher ranked substituents on oppositeopposite sides sides ZZ : : higher ranked substituents on higher ranked substituents on samesame side side
higherhigher
lowerlower
The E-Z Notational SystemThe E-Z Notational System
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CC CC
EE : : higher ranked substituents on higher ranked substituents on oppositeopposite sides sides ZZ : : higher ranked substituents on higher ranked substituents on samesame side side
higherhigher
lowerlower
The E-Z Notational SystemThe E-Z Notational System
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CC CC
EE : : higher ranked substituents on higher ranked substituents on oppositeopposite sides sides ZZ : : higher ranked substituents on higher ranked substituents on samesame side side
EntgegenEntgegen
higherhigher
higherhigherlowerlower
lowerlower
The E-Z Notational SystemThe E-Z Notational System
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CC CCCC CC
EE : : higher ranked substituents on higher ranked substituents on oppositeopposite sides sides ZZ : : higher ranked substituents on higher ranked substituents on samesame side side
EntgegenEntgegen ZusammenZusammen
higherhigher
higherhigherlowerlower
lowerlower
lowerlower
higherhigher
lowerlower
higherhigher
The E-Z Notational SystemThe E-Z Notational System
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CC CCCC CC
Answer: Answer: They are ranked in order of They are ranked in order of decreasing atomic number. decreasing atomic number.
EntgegenEntgegen ZusammenZusammen
higherhigher
higherhigherlowerlower
lowerlower
lowerlower
higherhigher
lowerlower
higherhigher
Question: How are substituents ranked?Question: How are substituents ranked?
The E-Z Notational SystemThe E-Z Notational System
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The Cahn-Ingold-Prelog (CIP) SystemThe Cahn-Ingold-Prelog (CIP) System
The system that we use was devised byThe system that we use was devised byR. S. CahnR. S. CahnSir Christopher IngoldSir Christopher IngoldVladimir PrelogVladimir Prelog
Their rules for ranking groups were devised in Their rules for ranking groups were devised in connection with a different kind of connection with a different kind of stereochemistry—one that we will discuss in stereochemistry—one that we will discuss in Chapter 7—but have been adapted to alkene Chapter 7—but have been adapted to alkene stereochemistry.stereochemistry.
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(1)(1) Higher atomic number outranks lower Higher atomic number outranks lower atomic numberatomic number
Br > FBr > F Cl > HCl > H
higherhigher
lowerlower
BrBr
FF
ClCl
HH
higherhigher
lowerlower
CC CC
Table 5.1 CIP RulesTable 5.1 CIP Rules
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(1)(1) Higher atomic number outranks lower Higher atomic number outranks lower atomic numberatomic number
Br > FBr > F Cl > HCl > H
((Z Z )-1-Bromo-2-chloro-1-fluoroethene)-1-Bromo-2-chloro-1-fluoroethene
higherhigher
lowerlower
BrBr
FF
ClCl
HH
higherhigher
lowerlower
CC CC
Table 5.1 CIP RulesTable 5.1 CIP Rules
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(2) When two atoms are identical, compare the (2) When two atoms are identical, compare the atoms attached to them on the basis of their atoms attached to them on the basis of their atomic numbers. Precedence is established atomic numbers. Precedence is established at the first point of difference. at the first point of difference.
——CCHH22CCHH33 outranks — outranks —CCHH33
——CC((CC,H,H),H,H)
Table 5.1 CIP RulesTable 5.1 CIP Rules
——CC(H,H,H)(H,H,H)
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(3) Work outward from the point of attachment, (3) Work outward from the point of attachment, comparing all the atoms attached to a comparing all the atoms attached to a particular atom before proceeding furtherparticular atom before proceeding furtheralong the chain. along the chain.
——CCH(H(CCHH33))22 outranks outranks —C—CHH22CCHH22OHOH
——CC((CC,,CC,H),H) ——CC((CC,H,H),H,H)
Table 5.1 CIP RulesTable 5.1 CIP Rules
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(4) (4) Evaluate substituents one by one. Evaluate substituents one by one. Don't add atomic numbers within groups.Don't add atomic numbers within groups.
——CCHH22OOH outranks H outranks —C—C(CH(CH33))33
——CC((OO,H,H),H,H) ——CC(C,C,C)(C,C,C)
Table 5.1 CIP RulesTable 5.1 CIP Rules
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(5)(5) An atom that is multiply bonded to another An atom that is multiply bonded to another atom is considered to be replicated as a atom is considered to be replicated as a
substituent on that atom.substituent on that atom.
——CCH=H=OO outranks outranks —C—CHH22OOHH
——CC((OO,,OO,H),H) ——CC((OO,H,H),H,H)
Table 5.1 CIP RulesTable 5.1 CIP Rules
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A table of commonly encountered A table of commonly encountered substituents ranked according to precedence substituents ranked according to precedence is given on the inside back cover of the text.is given on the inside back cover of the text.
Table 5.1 CIP RulesTable 5.1 CIP Rules