Chapter 18 Reactions of Aromatic molecules Benzene is aromatic: a cyclic conjugated compound with 6 electrons Reactions of benzene lead to the retention.

Chapter 18 Reactions of Aromatic molecules

•Benzene is aromatic: a cyclic conjugated compound with 6 electrons

•Reactions of benzene lead to the retention of the aromatic core

Types of Reactions

• Electrophilic substitution

• Diazonium chemistry

• Nucleophilic substitution

• Misc. modification of substituents

Electrophilic Substitution Reactions of Benzene and Its Derivatives

Electrophilic Substitution versus addition

Arenium ion: Wheland intermediateAlso called sigma complex

Energy diagram comparison of electrophilic substitution versus electrophilic addition

Is this kinetic or thermodynamic control?

Electrophilic Bromination of Aromatic Rings

ortho-bromotoluenepara-bromotoluenetoluene

meta-bromonitrobenzene

Regiochemistry (ortho, para, meta) will depend on relative stability of resonance structures for carbocation intermediates

Mechanism for Electrophilic Bromination of Aromatic Rings

ortho carbocation ortho carbocation

para carbocation

Electrophilic substitution of Bromobenzene

Halogens are ortho para directors, but are still deactivating compared with benzene

Transformations of Aryl bromides

Aromatic Nitration• The combination of nitric acid and sulfuric acid produces

NO2+ (nitronium ion)

• The reaction with benzene produces nitrobenzene

Gun solvent

Nitration of toluene: an electron rich monomer

ortho & para Regioselectivity explained

Kinetics are more favorable for ortho and para isomers with electron donating substitutent on benzene

Too corrosive for artillery shells

•High explosive: Shock wave•Secondary explosive: requires primer (primary explosive) to detonate•Nitroaromatics are harmful: aplastic anemia and liver toxicity

Reactions of nitroaromatics

• Nitro is deactivating (destabilizes the Wheland intermediate & slows reactions).

• Reactions are 100,000 slower than with benzene• Meta directing

More polynitrationmono-brominationReduction to anilines and azo

compoundsNucleophilic aromatic substitution

Meta selective: electron withdrawing groups

•electron withdrawing group inductively destabilizes adjacent carbocations in ortho and para cases. • No adjacent carbocation in meta regiochemistry resonance structures

Reduction of Nitroaromatics to Aryl amines

Amine group is electron donating: changes subsequent regiochemistry from meta to ortho-para

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

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

Alkylation of Aromatic Rings: The Friedel–Crafts Reaction

• Aromatic substitution of a R+ for H• Aluminum chloride promotes the formation of

the carbocation• Rearrangement of carbocation can occur

Friedel Craft alkylation mechanism

Friedel Craft alkylation with rearrangements

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)• Will not work with rings containing an amino group

substituent or a strongly electron-withdrawing group

Control Problems

• Multiple alkylations can occur because the first alkylation is activating

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

Friedel Craft Acylation Mechanism

Acylation – No rearrangement of acylium ions

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

Strongly Activating o,p directors: Multiple additions

Reduce reactivity with acetyl groups

Summary of activation versus deactivation and ortho & para versus meta direction

With multiple substitutents there can be antagonistic or reinforcing effects

Antagonistic or Non-Cooperative

D = Electron Donating Group (ortho/para-directing)W = Electron Withdrawing Group (meta-directing)

Reinforcing or Cooperative

Multiple Substituents in antagonistic systems

The most strongly activating substituent will determine the position of the next substitution. May have mixtures.

OCH3

O2N

SO3

H2SO4

OCH3

O2N

SO3H

OCH3

O2N

SO3H

+

=>

Sulfonic acid blocking groups

?

?

Electrophilic substitution reaction used to make plastics

Bakelite, NovolacAcid or base catalyzed reactions

Acid catalyzed reaction of phenol with formaldehyde

Electrophilic substitution reaction used to make plastics

Acid catalyzed reaction of phenol with formaldehyde

Electrophilic substitution reaction used to make plastics

Base catalyzed reaction of phenol with formaldehyde

Nucleophilic Aromatic Substitution

• While protons attached to electron-rich aromatics can be displaced by electrophiles, halogens attached to electron-depleted aromatics can be displaced by nucleophies

• Nucleophilic aromatic substitution is similar to SN1/SN2 in its outcome, but follows completely different mechanisms

Substitution Nucleophilic Aromatic (SNAr), the Benzyne Mech, and reaction of diazonium salts

SNAr Mechanism: Electron EWG’s

Addition-Elimination Reactions

• Typical for aryl halides with nitro groups in ortho or para position

• Addition to form intermediates (Meisenheimer complexes) by electron-withdrawal

• Halide ion is then lost by elimination

Chlorobenzene is unreactive under ordinary laboratory conditions…

…but brute force will do the job!

However, this can’t be the same mechanism

Nucleophilic substitution aromatic

Strong EWG ortho or para to leaving group (F, Cl, Br, I, OTf)

Strong nucleophile (HO-, RO-, Amide, thiolate, carbanions)

SNAr used in making polymers (plastics)

Elimination-Addition: Benzynes • The reaction involves an elimination reaction that gives a

triple bond, followed by rapid addition of water

• The intermediate is called benzyne

Evidence for Benzyne as an Intermediate

• Bromobenzene with 14C only at C1 gives substitution product with label scrambled between C1 and C2

• Reaction proceeds through a symmetrical intermediate in which C1 and C2 are equivalent— must be benzyne

Structure of Benzyne• Benzyne is a highly distorted alkyne• The triple bond uses sp2-hybridized carbons, not the usual

sp• The triple bond has one bond formed by p–p overlap and

by weak sp2–sp2 overlap

Another Nucleophilic Like reaction using Diazonium Salts (made from Anilines)

ArNH2 is easily made from reduction of nitrobenzenes. Permits preparation of molecules impossible to make otherwise

Mechanism for formation of Diazonium Salts from Anilines

Three possible reaction mechanisms for Nucleophilic substitution reactions with Diazonium salts

Thermal ionization (like SN1)

Organometallic

Redox (radical intermediate)

e.g. Formation of phenol

e.g. Sandmeyer reaction

62

Diazonium chemistry

16.10 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, ArR ArCO2H

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

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

16.11 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)

Summary of reactions not involving aromatic substitution

• Reduction of nitrobenzenes to anilines• Conversion of benzenesulfonic acids to phenols• Side chain oxidation of alkylbenzenes to benzoic

acids• Side chain halogenation of alkylbenzenes• Reduction of benzenes to cyclohexanes• Reduction of aryl ketones to alkyl benzenes