Electophilic Aromatic Substituionwebpages.iust.ac.ir/naimi/Lectures/Organic... · An interplay of...
Transcript of Electophilic Aromatic Substituionwebpages.iust.ac.ir/naimi/Lectures/Organic... · An interplay of...
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Organic Chemistry
M. R. Naimi-Jamal
Faculty of Chemistry
Iran University of Science & Technology
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Chapter 5-2. Chemistry of Benzene: Electrophilic Aromatic Substitution
Based on McMurry’s Organic Chemistry, 6th edition, Chapter 16
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Substitution Reactions of Benzene and Its Derivatives
Benzene is aromatic: a cyclic conjugated compound with 6 electrons
Reactions of benzene lead to the retention of the aromatic -system
Electrophilic aromatic substitution replaces a
proton on benzene with another electrophile
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Bromination of Aromatic Rings
Benzene’s electrons participate as a Lewis base in reactions with Lewis acids
The product is formed by loss of a proton, which is replaced by bromine
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Bromination of Aromatic Rings
FeBr3 is added as a catalyst to polarize the bromine reagent
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Cationic Intermediate in Bromination
The addition of bromine occurs in two steps
In the first step the electrons act as a nucleophile toward Br2 (in a complex with FeBr3)
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This forms a cationic addition intermediate
The intermediate is not aromatic and therefore high in energy
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Formation of Product from Intermediate
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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Other Aromatic Substitutions
The reaction with bromine involves a mechanism that is similar to many other reactions of benzene with electrophiles
The cationic intermediate was first proposed by G. W. Wheland of the University of Chicago and is often called the Wheland intermediate
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Aromatic Chlorination and Iodination
Chlorine and iodine (but not fluorine, which is too reactive) can produce aromatic substitution in the presence of Lewis acids.
Chlorination requires FeCl3
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Aromatic Chlorination and Iodination
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), which
is isoelectronic with CO2
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Aromatic Nitration
The reaction with benzene produces nitrobenzene
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Reduction of nitro compounds to amines
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Aromatic Sulfonation
Substitution of H by SO3 (sulfonation)
Reaction with a mixture of sulfuric acid and SO3 (fuming sulfuric acid)
Reactive species is sulfur trioxide or its conjugate acid
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Aromatic Sulfonation
Sulfur trioxide, or its conjugate acid, react
by the usual mechanism:
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Useful reactions of sulfonic acids
Sulfonic acids are useful as intermediates in the
synthesis of sulfa drugs and phenols:
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Alkylation of Aromatic Rings: The Friedel–Crafts Reaction
Aromatic substitution of “R+” for H,
alkylating the ring
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Alkylation of Aromatic Rings: The Friedel–Crafts Reaction
Aromatic substitution of a R+ for H
Aluminum chloride promotes the formation of the carbocation
Wheland intermediate forms
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Limitations of the Friedel-Crafts Alkylation
Only alkyl halides can be used (F, Cl, I, Br)
Aryl halides and vinylic halides do not react
(their carbocations are too hard to form)
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Limitations of the Friedel-Crafts Alkylation
Will not work with rings containing an amino
group substituent or a strongly electron-
withdrawing group
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Control Problems
Multiple alkylations can occur because the
first alkylation is activating
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Carbocation Rearrangements During Alkylation
Similar to those that occur during electrophilic additions to alkenes
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Similar reactions:
Mechanism?
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Solution:
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Another variation:
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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
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Mechanism of Friedel-Crafts Acylation
Similar to alkylation; reactive electrophile is a
resonance-stabilized acyl cation, which does
not rearrange
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Problem: acid chloride reactant?
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Substituent Effects in Aromatic Rings
Substituents can cause a compound to be (much) more or (much) less reactive than benzene
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Substituent Effects in Aromatic Rings
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 s 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
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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 s 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
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Resonance Effects – Electron Withdrawal
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Resonance Effects – Electron Donation
Halogen, OH, alkoxyl (OR), and amino substituents donate electrons
Effect is greatest at ortho and para
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Resonance Effects – Electron Donation
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Contrasting Effects
Halogen, OH, OR, withdraw electrons
inductively so that they deactivate the
ring
Resonance interactions are generally
weaker, affecting orientation
The strongest effects dominate
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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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Electron Donation & Withdrawal from Benzene Rings
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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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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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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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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 Table: Effect of Substituents in Aromatic Substitution
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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
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Meta-Disubstituted Compounds Are Unreactive between the two groups
The reaction site is too hindered
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Prob.: Substitution at which positions?
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Prob.: Major substitution product(s)?
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Oxidation of Aromatic Compounds
Alkyl side chains can be oxidized to CO2H by strong reagents such as KMnO4 and Na2Cr2O7 if they have a C-H next to the ring
Converts an alkylbenzene into a benzoic acid
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Prob.: Oxidation products?
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Bromination of Alkylbenzene Side Chains
Reaction of an alkylbenzene with N-bromo-succinimide (NBS) and benzoyl peroxide (radical initiator) introduces Br into the side chain
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Mechanism of NBS (Radical) Reaction
Abstraction of a benzylic hydrogen atom
generates an intermediate benzylic
radical
Reacts with Br2 to yield product
Br· radical cycles back into reaction to
carry chain
Br2 produced from reaction of HBr with
NBS
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Mechanism of NBS (Radical) Reaction
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Benzylic Radical:
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Reduction of Aromatic Compounds
Aromatic rings are inert to catalytic hydrogenation under
conditions that reduce alkene double bonds
Can selectively reduce an alkene double bond in the
presence of an aromatic ring
Reduction of an aromatic ring requires more powerful
reducing conditions (high pressure or rhodium catalysts)
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Reduction of Aryl Alkyl Ketones
Aromatic ring activates neighboring carbonyl
group toward reduction
Ketone is converted into an alkylbenzene by
catalytic hydrogenation over Pd catalyst
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Synthesis Strategies
These syntheses require planning and
consideration of alternative routes
Work through the practice problems in this
section following the general guidelines for
synthesis and retrosynthetic analysis.
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Practice Problem:
Synthesize From Benzene:
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Solutions:
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Practice Problem:
Synthesize From Benzene:
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How can we make m-chloropropylbenzene?
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Putting it all together:
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Prob.: What’s wrong with these syntheses?
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Prob.: What’s wrong with these syntheses?
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Prob.: Synthesize from benzene
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Prob.: Identify the reagents
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Chapter 5-2, Questions
27, 33, 35, 41, 42
45, 51