2013 lect5 elect_aromatik substitution
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...TRANSCRIPT
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Reactivity of Benzene
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Benzene’s Unusual Structure
All its C-C bonds are the same length: 139 pm — between single (154 pm) and double (134 pm) bonds, which means that electron density in all six C-C bonds is identical
Structure is planar, hexagonal, thus C–C–C bond angles is 120° Each C is sp2 and has a p orbital perpendicular to the plane of
the six-membered ring
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Stability of Benzene
Benzene is a cyclic compound that consists of six carbon atoms bonded together by σ bonds and a set of delocalized π bonds.
All the electrons associated with those π bonds delocalize over all six carbons.
Delocalized electrons in a cyclic conjugated system have a dramatic effect on the stability of the molecule.
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HEATS OF HYDROGENATION AS INDICATORS OF STABILITY
Therefore C6H6 has about 150 kJ more “stability” than an isolated set of three double bonds (See Figure 15-2)
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Stability of BenzeneIn fact, this stability makes aromatic molecules so unreactive that they do not follow the expected reaction pathways that their structures suggest they should.
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Electrophilic Aromatic Substitution
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Substitution Reactions of Benzene
Electrophilic aromatic substitution replaces a proton on benzene with another electrophile
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Bromination of Aromatic Rings
FeBr3 is added as a catalyst to polarize the bromine reagent
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INTERMEDIATE IN BROMINATION
Benzene’s electrons participate as a Lewis base (act as a nucleophile) toward Br2 (in a complex with FeBr3)
This reaction forms a cationic addition intermediate
The intermediate is not aromatic and therefore high in energy.
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FORMATION OF PRODUCT
The cationic addition intermediate transfers a proton to FeBr4
- (from Br- and FeBr3)
This restores aromaticity (in contrast with addition in alkenes)
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AROMATIC CHLORINATION/IODINATION
Chlorine and iodine (but not fluorine, which is too reactive) can produce aromatic substitution with the addition of other reagents to promote the reaction
Chlorination requires FeCl3 Iodine must be oxidized to form a more powerful I+
species (with Cu+ or peroxide)
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AROMATIC NITRATION The combination of nitric acid and sulfuric acid
produces NO2+ (nitronium ion)
The reaction with benzene produces nitrobenzene
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AROMATIC SULFONATION Substitution of H by SO3 (sulfonation) Reaction with a mixture of sulfuric acid and SO3 Reactive species is sulfur trioxide or its conjugate acid Reaction occurs via Wheland intermediate and is
reversible
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Alkali Fusion of Aromatic Sulfonic Acids
Sulfonic acids are useful as intermediates Heating with NaOH at 300 ºC followed by
neutralization with acid replaces the SO3H group with an OH
Example is the synthesis of p-cresol
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AROMATICALKYLATION The Friedel–Crafts Reaction
Aluminum chloride promotes the formation of the carbocation
Wheland intermediate forms
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Many ways of CARBOCATION FORMATION
CH3 CH CH3
Cl
+ AlCl3
CH3C
H3C H
Cl AlCl3+ _
H2C CH CH3
HFH3C CH CH3
F+
_
H3C CH CH3
OHBF3
H3C CH CH3
OH BF3+
H3C CH CH3+
+ HOBF3
_
=>
AROMATIC ALKYLATION
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Formation of Alkyl Benzene
C
CH3
CH3
H+
H
H
CH(CH3)2+
H
H
CH(CH3)2
B
F
F
F
OHCH
CH3
CH3
+
HF
BF
OHF
=>
+
-
AROMATIC ALKYLATION
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CARBOCATION REARRANGEMENTS During Alkylation
Similar to those that occur during electrophilic additions to alkenes
Can involve H or alkyl shifts
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Carbocation Rearrangements During Alkylation
Similar to those that occur during electrophilic additions to alkenes
Can involve H or alkyl shifts
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ACYLATION OF AROMATIC RINGS
Reaction of an acid chloride (RCOCl) and an aromatic ring in the presence of AlCl3 introduces acyl group, COR Benzene with acetyl chloride yields acetophenone
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FRIEDEL-CRAFTS ACYLATION
Similar to alkylation Reactive electrophile: resonance-stabilized acyl cation An acyl cation does not rearrange
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FORMYLATIONGatterman-Koch
Formyl chloride is unstable. Use a high pressure mixture of CO, HCl, and catalyst.
Product is benzaldehyde.
CO + HCl H C
O
ClAlCl3/CuCl
H C O+
AlCl4
_
C
O
H
+ C
O
H+ HCl+
=>
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SUMMARY
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Reaksi elektrofilik aromatik10.27 sampai 10 2910.48
Soal tantangan
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SUBSTITUENT EFFECTS IN ELECTROFILIC AROMATIC
SUBTITUTION
DEACTIVATOR
ACTIVATOR
Meta-Directing
Ortho- and Para-Directing
Inductive effects
Resonance effect
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EFFECT OF SUBSTITUENT on Friedel-Crafts Alkylation
Alkylation will not work with rings containing an amino group substituent or a strongly electron-withdrawing group
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On the other hand multiple alkylations occur and become a major products
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SUBSTITUENT EFFECTS IN AROMATIC RINGS
Substituents can cause a compound to be (much) more or (much) less reactive than benzene
Substituents affect the orientation of the reaction – the positional relationship is controlled ortho- and para-directing activators, ortho- and para-directing
deactivators, and meta-directing deactivators
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ORIGINS OF SUBSTITUENT EFFECTS
An interplay of inductive effects and resonance effects
Inductive effect - withdrawal or donation of electrons through a bond
Resonance effect - withdrawal or donation of electrons through a bond due to the overlap of a p orbital on the substituent with a p orbital on the aromatic ring
RESONANSI, PERGESERAN ELEKTRON, STRUKTUR RESONANSI (penyumbang utama, penyumbang tambahan), STABILISASI RESONANSI (bab 1 hal.70-77)
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Inductive Effects Controlled by electronegativity and the polarity of
bonds in functional groups Halogens, C=O, CN, and NO2 withdraw electrons
through bond connected to ring Alkyl groups donate electrons
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Resonance Effects – Electron Withdrawal
C=O, CN, NO2 substituents withdraw electrons from the aromatic ring by resonance
electrons flow from the rings to the substituents
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Resonance Effects – Electron Donation
Halogen, OH, alkoxyl (OR), and amino substituents donate electrons
electrons flow from the substituents to the ring Effect is greatest at ortho and para
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An Explanation of Substituent Effects
Activating groups donate electrons to the ring, stabilizing the Wheland intermediate (carbocation)
Deactivating groups withdraw electrons from the ring, destabilizing the Wheland intermediate
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Ortho- and Para-Directing Activators: Alkyl Groups Alkyl groups activate/direct further substitution to positions
ortho and para to themselves Alkyl group is most effective in the ortho and para positions
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Energy Diagram
=>
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Ortho- and Para-Directing Activators: OH and NH2 Alkoxyl, and amino groups have a strong, electron-
donating resonance effect Most pronounced at the ortho and para positions
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Summary ofActivators
=>
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Ortho- and Para-Directing Deactivators: Halogens Electron-withdrawing inductive effect outweighs
weaker electron-donating resonance effect Resonance effect is only at the ortho and para
positions, stabilizing carbocation intermediate
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Summary ofActivators
=>
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Deactivating Meta-Directing Substituents Electrophilic substitution reactions for
nitrobenzene are 100,000 times slower than for benzene.
The product mix contains mostly the meta isomer, only small amounts of the ortho and para isomers.
Meta-directors deactivate all positions on the ring, but the meta position is less deactivated. =>
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Ortho Substitutionon Nitrobenzene
=>
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Para Substitution on Nitrobenzene
=>
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Meta Substitutionon Nitrobenzene
=>
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Energy Diagram
=>
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Meta-Directing Deactivators
Inductive and resonance effects reinforce each other Ortho and para intermediates destabilized by
deactivation from carbocation intermediate Resonance cannot produce stabilization
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Summary of Deactivators
=>
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More Deactivators
=>
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Summary Table: Effect of Substituents in Aromatic Substitution
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Summary of Directing Effects
=>
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Soal tantangan
Pengaktifan cincin benzena10.3010.34
Pengarahan orto para10.3110.3210.33
Efek dari substituen10.50
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TRISUBSTITUTED BENZENES
Br
CH2CH3
NO2
OH
Cl
Br
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Trisubstituted Benzenes: Additivity of Effects If the directing effects of the two groups are the
same, the result is additive
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Substituents with Opposite Effects
If the directing effects of two groups oppose each other, the more powerful activating group decides the principal outcome
Often gives mixtures of products
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Meta-Disubstituted Compounds Are Unreactive The reaction site is too hindered To make aromatic rings with three adjacent
substituents, it is best to start with an ortho-disubstituted compound
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Soal tantangan
Substitusi ke 310.3610.3710.3810.3910.49
10.5110.52
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Jalur Reaksi mana dipilih?
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Reaksi mana dipilih?
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NUCLEOPHILIC AROMATIC
SUBSTITUTION
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NUCLEOPHILICAROMATIC SUBSTITUTION
A nucleophile replaces a leaving group on the aromatic ring.
Electron-withdrawing substituents activate the ring for nucleophilic substitution.
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Aryl Halides and Nucleophilic Aromatic Substitution
Simple aryl and vinyl halides do not undergo nucleophilic substitution
Back-side attack required for SN2 reaction is blocked in aryl halides
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SN2 reaction also doesn’t occur in aryl (and vinyl halides) because the carbon-halide bond is shorter and stronger than in alkyl halides
Bonds to sp2-hybridized carbons are shorter, and therefore stronger, than to sp3-hybridized carbons
Resonance gives the carbon-halogen bond some double bond character
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Nucleophilic substitution can occur on benzene rings when strong electron-withdrawing groups are ortho or para to the halogen atom
The more electron-withdrawing groups on the ring, the lower the temperature required for the reaction to proceed
Nucleophilic Aromatic Substitution by Addition-Elimination: The SNAr Mechanism
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The carbanion is stabilized by electron-withdrawing groups in the ortho and para positions
addition-elimination mechanism
A Meisenheimer complex, which is a delocalized carbanion, is an intermediate
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Addition-EliminationMechanism
=>
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NUCLEOPHILIC AROMATIC SUBSTITUTION
Aryl halides with electron-withdrawing substituents ortho and para react with nucleophiles
Form addition intermediate (Meisenheimer complex) that is stabilized by electron-withdrawal
Halide ion is lost to give aromatic ring
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Soal tantangan
Substitusi nukleofilik10.14
Sintesis10.4510.4610.47
Sintesis10.5310.5410.5510.5610.5710.58