benzene
TRANSCRIPT
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BENZENE AND DERIVATIVES
MEMBERS GROUP :NUR HIDAYAH BADARUDDIN
SYAZANA ISMAILNOOR AZURAH ABDUL
RAZAKIRA NUSRAT JAAFAR
NOR FADILAH ZAKARIA
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INTRODUCTION
• Benzene is a chemical that is a colourless or light yellow liquid at room temperature. It has a sweet odour and is highly flammable.
• Natural sources of benzene include volcanoes and forest fires. Benzene is also a natural part of crude oil, gasoline, and cigarette smoke.
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Michael Faraday• The word "benzene" derives
historically from "gum benzoin", sometimes called "benjamin" an aromatic resin known to European pharmacists and perfumers since the 15th century as a product of southeast Asia.
• Michael Faraday first isolated and identified benzene in 1825 from the oily residue derived from the production of illuminating gas, giving it the name bicarburet of hydrogen.
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IUPAC NOMENCLATURE
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a) MONOSUBSTITUTION
• 1) Benzene as the parent name:
ethylbenzene chlorobenzene bromobenzene
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2)Common name:
styrene toluene
cymene
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3)Alkyl substituent is larger than ring:
3-phenyldecane
5-phenylpentanoic acid
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b) DISUBSTITUTION
• 1)Ortho- disubstituted benzene has two substituent in a 1,2 positions:
• Principle functional group is the benzene therefore root = benzene
• There are two chlorine substituent therefore dichloro.
• The substituent locants are 1 and 2 therefore ortho.
O-dichlorobenzene
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2) Meta -disubstituted benzene has two substituents in a 1,3 positions:
• Principle functional group is the benzne therefore root = benzene
• There is a chlorine substituent therefore chloro.
• There is a bromine substituent therefore bromo.
• The substituent locants are 1 and 3 therefore meta.
m-bromochlorobenzene
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3) Para-disubstituted benzene has two substituents in a 1,4 positions:
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Polydisubstituted benzene derivatives:
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c) POLYSUBSTITUTION
• Benzene with more than 2 substituents are named by numbering the position of each substituent with lowest possible numbers:
• Principle functional group is the aromatic amine therefore = aniline
• There is a C1 substituent therefore methyl• There is a C2 substituent therefore ethyl• Numbering from the -NH2 (priority group at C1)
gives the substituents the locants =2 and 3
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2-ethyl-3-methylaniline
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Physical Properties of Benzene
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1.The Kekulé Structure of Benzene
• German chemist Friedrich August Kekulé von Stradonitz
• A structure of benzene, containing 3 cyclic conjugated double bonds which systematically called 1,3,5-cyclohexatriene
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• The true structure of benzene is a resonance hybrid of the two Lewis structures, with the dashed lines of the hybrid indicating the position of the π bonds.
hybrid
Cont.
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2.Stability
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• Benzene does not undergo addition reactions typical of other highly unsaturated compounds, including conjugated dienes.
• Benzene does not react with Br2 to yield an addition product. Instead, in the presence of a Lewis acid, bromine substitutes for a hydrogen atom, yielding a product that retains the benzene ring.
Cont.
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3.Boiling Point• The only attractions between neighbouring molecules are van der Waals
dispersion forces.• Benzene boils at 80°C -
o-dichlorobenzeneb.p. 1810C
m-dichlorobenzeneb.p. 1730C
p-dichlorobenzeneb.p. 1700C
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4. The Criteria for Aromacity : Hückel's Rule
• 4 structural criteria must be satisfied for a compound to be aromatic:
a) Cyclicb) Planarc) Completely Conjugatedd) Contain a particular number of π electrons
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[4] A molecule must satisfy Hückel’s rule, which requires a particular number of electrons.
•Benzene is aromatic and especially stable because it contains 6 electrons.
Hückel's rule:
•Cyclobutadiene is antiaromatic and especially unstable because it contains 4 electrons.
Cont.
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Note that Hückel’s rule refers to the number of electrons, not the number of atoms in a particular ring.
Cont.
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REACTION OF BENZENE
An electrophile (E⁺) reacts with an aromatic ring and substitutes for one of the hydrogen
Benzene does not undergo addition reactions because addition would yield a product that is not aromatic
Electrophilic Aromatic substituent
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Aromatic Halogenation
Aromatic Nitration
Friel-Crafts Alkylation
Friel-Crafts Acylation
Aromatic sulfonation
5 MAIN ELECTROPHILIC SUBSTITUENT
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GENERAL MECHANISM
Step 1 : Formation of arenium ionPositive ion X+ = electrophile
Example :
Step 2 : Loss of H +
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AROMATIC HALOGENATION
Reactants : Benzene and halogens (Clorine or Bromine)Conditions : Lewis acid like FeCl₃ or FeBr₃Analogous reaction with I2 and F2 are not synthetically useful because I2 is too unreactive and F2 is too violently
Electrophile : Cl⁺ or Br⁺ Example :
+ Br₂ no reaction (decolorization not observed)
+
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MECHANISM :
(The electrophile attacks the π electron system of the benzene ring to form a arenium ion)
Step 1 : Formation of Cl⁺ or Br⁺
Step 2 : Electrophilic substitution
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bromobenzene
Function of Lewis acid : Incerase the polarity of halogen molecules to produce positive halogen ions (Cl⁺ or Br⁺) = electrophile
Step 3 : Loss of proton to reform the aromatic ring
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AROMATIC NITRATION
Reactants : Benzene and concentrated HNO₃Conditions : Concentrated H₂SO₄
Example :
nitrobenzene
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MECHANISM :
- Sulfuric acid ionizes to produce a proton
-Nitric acid accepts a proton from a stronger acid (H₂SO₄) and form a protonated nitric acid
- The protonated nitric acid dissociates to form a nitronium ion (+NO2)
Step 1 : Formation of Nitronium ion (NO₂⁺)
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Step 2 : Electropjilic substitution
Step 3 : Loss of proton to re-form the aromatic ring
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Reactants : Benzene and alkyl halideCondition : catalyst (Lewis acid like AlCl₃)
+
FRIEDEL-CRAFT ALKYLATION
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Example :
1)
2)
AlCl₃
tolouene
Tert-butylbenzene
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MECHANISM :Step 1 : Formation of carbocation
Step 2 : Electrophilic substitution (electrophile attacks the π electron system of the benzene ring to form an arenium ion)
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Step 3 : loss of proton to re-form the aromatic ring
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Friedel-Craft Acylation
Reactancts: Aromatic rings and acid chloride
Product: KetoneCondition: Strong Lewis acid
Benzene
Acid chloride
Ketone
AlCl3
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Example:
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Mechanism:
Step 1: Dissociation of a chloride ion to form an acyl cation ("acylium ion")
Step 2: The resulting acylium ion or a related adduct is subject to nucleophilic attack by the arene
Step 3:Chloride anion (or AlCl4-) deprotonates the ring (an "arenium ion") to form HCl, and the AlCl3 catalyst is regenerated
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Aromatic Sulfonation
Organic reaction in which a hydrogen atom on an arene is replaced by a sulfonic acid functional group in an electrophilic aromatic substitution
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Mechanism:
Step 1: The p electrons of the aromatic C=C act as a nucleophile, attacking the electrophilic S, pushing charge out onto an electronegative O atom. This destroys the aromaticity giving the cyclohexadienyl cation intermediate.
Step 2: Loss of the proton from the sp3 C bearing the sulfonyl- group reforms the C=C and the aromatic system.
Step 3: Protonation of the conjugate base of the sulfonic acid by sulfuric acid produces the sulfonic acid.
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Substituent Effect in Substituted Aromatic Benzene
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Effect of Substituent
Orientation
Ortho-Para
Meta
Reaction Rate
Activating
Deactivating
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Orientation
Ortho-substitution-2 substituents occupy
positions next to each other.
Para-substitutionSubstituent occupy positions 1 and 4
Meta-substitution - Substituent occupy positions 1 and 3
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Activating Group & Deactivating Group
Activating Group: Substituent that activate the ring, making it more reactive than benzene
Deactivating Group: Substituent that deactivate ring, making it less reactive than benzene
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Ortho-Para Activator
Electron donating groups (EDG) with lone pairs on the atoms adjacent to the p system activate the aromatic ring by increasing the electron density on the ring through a resonance donating effect.
The resonance only allows electron density to be positioned at the ortho- and para- positions.
Hence these sites aremore nucleophilic, and the system tends to react with electrophiles at these ortho- and para- sites.
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Examples:
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Example:
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Meta –Directing Deactivator
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Meta-Directing
Dea
ctiva
tor i
ncre
ase
-COR-CO2R-SO3H-CHO-CO2H-CN-NO2
-NR2+
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Explanation of meta- deactivators
Meta directors slow the reaction by raising the energy of the
carbocation intermediate because they have (in one resonance
form, shown below) a positively charged atom attached to the
ring. Two positively charged atoms so close together is very
high in energy (especially unstable).
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SOME EXAMPLES OF "META DIRECTORS“
the acyl group in benzaldehyde
the NO2 group in nitrobenzene
acyl , -CN , -SO3H , CF3 , and -NO2 are meta directors and deactivate the ring toward electrophilic aromatic substitution.
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HALOGENATION OF ALKYLBENZENE SIDE CHAIN
Side chain bromination at the benzylic position occurs when aklybenzene is treated with N-bromosuccinimide (NBS)
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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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Free radical also occurs between alkylbenzene side chain with halogen in the presence of heat or light (hv)
CH3 + Cl2
hv CH2Cl
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OXIDATION OF ALKYLBENZENE
•Alkyl Benzene ring is inert to strong oxidizing agents such as KMnO4 and chromic reagent•side chains react readily with oxidizing agents are converted into carbonyl group –COOH (Benzoic acid)
CH3 KMnO4 COOH
KMnO4 COOHCH2 CH3
CH3 KMnO4 COOHH3C COOH
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THE END…THANK YOU