Chapter 6 Alkenes and Alkynes I: Structure and Preparation.
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Transcript of Chapter 6 Alkenes and Alkynes I: Structure and Preparation.
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Chapter 6Alkenes and Alkynes I:
Structure and Preparation
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Alkene - Hydrocarbon With Carbon-Carbon Double Bond
• Also called an olefin but alkene is better• Includes many naturally occurring materials
– Flavors, fragrances, vitamins• Important industrial products
– These are feedstocks for industrial processes
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Nomenclature
• Suffix “-ene”
• Find longest continuous carbon chain containing the double bond for root name
• Number carbons in chain so that double bond carbons have lowest possible numbers
• Rings have “cyclo” prefix
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Many Alkenes Are Known by Common Names
• Ethylene = ethene• Propylene = propene• Isobutylene = 2-
methylpropene• Isoprene = 2-methyl-
1,3-butadiene
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Name the following Alkenes
CH2 CHCH2CH2CHCH3
CH3 CH3
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6.4 Electronic Structure of Alkenes
• Carbon atoms in a double bond are sp2-hybridized– Three equivalent orbitals at 120º separation in plane– Fourth orbital is atomic p orbital
• Combination of electrons in two sp2 orbitals of two atoms forms bond between them
• Additive interaction of p orbitals creates a bonding orbital– Subtractive interaction creates a anti-bonding orbital
• Occupied orbital prevents rotation about -bond• Rotation prevented by bond - high barrier, about 268 kJ/mole
in ethylene
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6.5 Cis-Trans Isomerism in Alkenes
• The presence of a carbon-carbon double can create two possible structures– cis isomer - two similar
groups on same side of the double bond
– trans isomer similar groups on opposite sides
• Each carbon must have two different groups for these isomers to occur
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Cis or Trans?
C CCH3
H
CH2CH3
HC C
CH3 CH3
CH2CH2CH3H
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Cis, Trans Isomers Require That End Groups Must Differ in Pairs
• 180°rotation superposes
• Bottom pair cannot be superposed without breaking C=C
X
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6.6 Sequence Rules: The E,Z Designation
• Neither compound is clearly “cis” or “trans”– Substituents on C1 are
different than those on C2
– We need to define “similarity” in a precise way to distinguish the two stereoisomers
• Cis, trans nomenclature only works for disubstituted double bonds
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Develop a System for Comparison of Priority of Substituents
• Assume a valuation system– If Br has a higher “value”
than Cl
– If CH3 is higher than H
• Then, in A, the higher value groups are on opposite sides
• In B, they are on the same side– Requires a universally
accepted “valuation”
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E,Z Stereochemical Nomenclature
• Priority rules of Cahn, Ingold, and Prelog
• Compare where higher priority group is with respect to bond and designate as prefix
• E -entgegen, opposite sides
• Z - zusammen, together on the same side
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Ranking Priorities: Cahn-Ingold-Prelog Rules
• Must rank atoms that are connected at comparison point• Higher atomic number gets higher priority
– Br > Cl > O > N > C > H
In this case,The higher priority groups are opposite:(E )-2-bromo-2-chloro-propene
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• If atomic numbers are the same, compare at next connection point at same distance
• Compare until something has higher atomic number• Do not combine – always compare
Extended Comparison
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• Substituent is drawn with connections shown and no double or triple bonds
• Added atoms are valued with 0 ligands themselves
Dealing With Multiple Bonds
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18Francis A. Carey, Organic Chemistry, Fourth Edition. Copyright © 2000 The McGraw-Hill Companies, Inc. All rights reserved.
Structure and bonding in ethyleneFigure 5.1
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6.7 Alkene Stability
• Cis alkenes are less stable than trans alkenes• Compare heat given off on hydrogenation: Ho
• Less stable isomer is higher in energy– And gives off more heat– tetrasubstituted > trisubstituted > disubstituted >
monosusbtituted– hyperconjugation stabilizes alkyl
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Prepartion of Alkenes
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Dehydration of an Alcohol
CH3
CH3
CH3C
OH
+ H2SO4 CH2
H3CC
H3C
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23Francis A. Carey, Organic Chemistry, Fourth Edition. Copyright © 2000 The McGraw-Hill Companies, Inc. All rights reserved.
Orbital description of the E2 mechanismFigure 5.10
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24Francis A. Carey, Organic Chemistry, Fourth Edition. Copyright © 2000 The McGraw-Hill Companies, Inc. All rights reserved.
Elimination by the E1 mechanismFigure 5.12
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26Francis A. Carey, Organic Chemistry, Fourth Edition. Copyright © 2000 The McGraw-Hill Companies, Inc. All rights reserved.
Bonding in acetyleneFigure 9.2