Polycyclic and Heterocyclic Aromatic Compounds
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Transcript of Polycyclic and Heterocyclic Aromatic Compounds
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CHAPTER 19
Polycyclic And Heterocyclic Aromatic
Compounds
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Nomenclature of Polycyclic Aromatic Compounds
Polycyclic aromatic compounds have two or more benzene rings fused together
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Monosubstituted Naphthalene is often designated by Greak Letter
NO2α
α α
α
β
ββ
β1-nitronaphthaleneβ-nitronaphthalene
Cl
Cl
OH
2-naphtholβ-naphthol
1,5-dichloronaphthalene
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More NamingBr
Br
9,10-dibromoanthracene
OCH3
OCH3
9,10-dimethoxy phenanthrene
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Bonding in Polycyclic Aromatic Compounds
• In benzene, all C-C bond lengths are equal ( equal distribution of pi electrons around the benzene ring).
• In the polycyclic aromatic compounds, the C-C bond lengths are not the same ( e,g. the distance between carbon 1 and 2 =1.36 A° in naphthalene is smaller than the distance between Carbon 2 and 3 = 1.40 A°) there is no equal distribution of pi electrons around naphthalene
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Comparison of bond lengths in Naphthalene
1.36 A
1.39 A
1,42 A
1.40 A
o
o
o
o
C-C in ethane: 1.54 A°
C-C in ethylene: 1.34 A°
C-C in benzene: 1.40 A°
12
345
6
78
Two out of three resonance structures show a carbon 1 carbon 2 double bond
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Resonance Energy of Polycyclic Aromatic Compounds
36 61 84 92 Kcal/mol
The resonance energy per ring is less than that of benzene suggest
• the polycyclic aromatic compounds are more reactive than benzene.
• reaction at one ring loses less energy because the product still have one or more intact benzenoid rings.
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Example
BrBr
Br2
Resonqance energy 92 36 X 2 = 72
The product still has two benzene rings ; it loses only 20 Kcal/mol
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Oxidation of Naphthalene• Naphthalene can be oxidized to products in
which much of the aromaticity is retained.
COH
COH
O
O
O
O
O
V2O5airheat
-H2O
O
O
CrO3
CH3CO2Hheat
1,4-naphthquinone
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Reduction of Polycyclic Aromatic Compounds
The polycyclic aromatic compounds (unlike benzene) can be hydrogenated without heat or pressure , or they can be reduced with sodium and ethanol
Na, CH3CH2OHheat
no reaction
Na, CH3CH2OHheat
Na, CH3CH2OHheat
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Hydrogenation of Polycyclic Aromatic Compounds
Hydrogenation of Polycyclic Aromatic Compounds requires heat and pressure just as it does for benzene
5 H2, pt35 atm, 250 co
5 H2, pt35 atm, 250 co
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Electrophilic Aromatic Substitution of Naphthalene
Naphthalene undergoes electrophilic aromatic substitution predominately at the 1-position (α-position)
Br2no catalyst
HNO3, H2SO4
Br
NO2
1-bromonaphthalene
1-nitronaphthalene
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More Electrophilic Aromatic Substitution Reactions
conc. H2SO4
80 c
CH3CCl
O
AlCl3
SO3H
CCH3O
1-naphthalene sulphonic acid
1- acetylnaphthalene
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Position of Substitution of Naphthalene
Br Br
step 1
slow
H Br
+ step 2
- H+, fast
Br
intermediate
1-substitution MechanismFavored
H Br
+
H Br
+
H Br
+
H Br
+
major contributors
Resonance structures for the 1- substitution intermediate
H Br
+
H Br+
H Br+7 resonance structures;
4 aromatics (major)
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2-position mechanism Not favoredBr Br
step 1
slow
Br
H step 2
- H+, fast
Br
intermediate
+
Resonance structures for the2- substitution intermediateBr
H+
Br
H+
major contributors
Br
H+
Br
H
+
Br
H
+
Br
H
+
Only 6 resonance structures; 2 aromatics
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Sulfonation of Naphthalene
+ SO3
fast
slow
SO3HSO3H
SO3HSO3H
80 C
160 Co
o+
+
91% 9 %
85 %15%Kinetic product
Thermodynamic product
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1-naphtalenesulphonic acid vs2- naphtalenesulphonic acid
SO3HHH
Repulsion
SO3H
H
H
less repulsion
1-naphtalenesulphonic acid 2-naphtalenesulphonic
acidLess stableMore stable
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Kinetic vs Thermodynamic Control
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Reactions ExamplesCH3
Br2
CH3
Br
CNNO2CN
NO2
+
CN
HNO3
H2SO4
The reaction occurs at the more activated ring
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Heterocyclic Aromatic Compounds
•Heterocyclic compounds have an element other than carbon as a member of the ring•Example of aromatic heterocyclic compounds are shown below– Numbering always starts at the heteroatom
N
N
H
1
2
34
5
imidazole
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Pyridine, a Six-MemberedAromatic Heterocycle
• Pyridine has an sp2 hybridized nitrogen.• The p orbital on nitrogen is part of the
aromatic π system of the ring.• The nitrogen lone pair is in an sp2 orbital
orthogonal to the p orbitals of the ring; these electrons are not part of the aromatic system.
• The lone pair on nitrogen is available to react with protons and so pyridine is basic
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Pyridine
Nα
ββ
α
γ
aromaticPyridine contain an electronegative nitrogen polar
Ν
δ+
δ−
Because the nitrogen is more electronegative than carbon, the rest of pyridine ring is electron deficient carbon atoms on the ring carry a partial positive charge pyridine has a low reactivity toward electrophilicsubstitution compared to benzene
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Reactions of Pyridine• Pyridine forms a cation with Lewis acids the
ring becomes even more electron deficient.
Ν
FeBr3
δ+
−
+
•Pyridine does not undergo Friedel- Crafts alkylationor Acylation.
•It does not undergo coupling with diazonium salts.
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Bromination of Pyridine• Bromination proceeds only at a high temperature
in the vapor phase by free radical path substitution occurs at the 3-position
N
Br2300o
N
Br
N
Br Br
+
3-bromopyridine37%
26%3,5-dibromopyridine
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Pyridine is basic• pKb of pyridine = 8.75 . It is less basic than
aliphatic amine (why?).• It undergo many reactions typical of amines
N+HCl- Pyridinium chloride
N
HCl
CH3ISN
2N+CH3 I-
N-methypyridiniumiodide
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Oxidation of alkyl pyridine
• The side chains in pyridine can be oxidized to carboxyl groups similar to alkyl benzene.
N
CO2H
N
CH2CH3KMnO4, H+
3-pyridinecarboxylic acid
3-ethylpyridine
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Nucleophilic Substitution on the Pyridine Ring
• Pyridine ring is electron deficient it is susceptible to nucleophilc attack.
• Nucleophilic substitution proceeds readily at the 2-position followed by the 4-position but not at the 3-position.
N Br
NH3heat N NH2
2-bromopyridine 2-aminopyridine
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Mechanism of substitution at the 2-position
N Br
NH3heat
- H+
NBr
NH2
-
NBr
NH2
-
NBr
NH2
-
- Br
N NH2
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Substitution at the 4-position
N
Cl
NH3heat
N
NH2
N
Br
CH3CH2O-
heatN
OCH2CH3
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Nucleophilic Substitution of pyridine
• Pyridine undergo nucleophilic substitution at the 2-position with extremely strong bases e.g. RLior NH2
-
N NH-
H2O
N NH2
+ OH-
NheatNH2
-
Nheat
RLi
N R
+ LiH
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Mechanism
NNH2
-N
NH2
H-
NNH2
H
-
NNH2
H
-
loss of H-
N NH H
+ H-
H2+N NHN NH2
H2OOH-
+
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Quinoline and Isoquinoline
N1
2
345
6
78
N1
2
345
6
78
isoquinolinequinoline
Both quinoline and isoquinoline contain a pyridine ring fused to a benzene ring
The nitrogen containing ring behaves like the pyridine ring.
The other ring behaves like naphthalene
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Electrophilic Substitution of Quinoline and Isoquinoline
• Both compounds undergo electrophlicsubstitution but in positions 5 and 8.
N
NO2
N
NO2
+
N
HNO3
H2SO4 N
NO2
N
NO2
+
N
HNO3H2SO4
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Reaction at the Nitrogen-Containing Ring of Quinoline and
Isoquinoline1. Both quinoline and isoquinoline (like
pyridine ) are weak bases ( pKb = 9.1 and 8.6 respectively.
2. Both compounds ( like pyridine) undergo nucleophilc substitution at the position α to the nitrogen.
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Examples
N
HCl
N
H+ Cl-
CH3IN N
CH3
+ I-
N
CH2CH3
+ Br-N
CH3CH2Br
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More Examples
N CH2CH3N
CH3CH2Li1)
2) H2O
NNH2
-1)
2) H2O N
NH2
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Five-membered Aromatic Heterocycle
In furan and thiophene an electron pair on the heteroatom is in a p orbital which is part of the aromatic system
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Pyrrole* This p orbital contains two electrons and participates in the aromatic system* The lone pair of pyrrole is part of the aromatic system and not available for protonation; pyrrole is therefore not basic
N H
N H + H+ no reaction
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Pyrrole Ring is Polar• The nitrogen atom in pyrrole contributes two
electrones to the aromatic pi cloud the nitrogen is electron deficient (not basic).
• The pyrrole ring is electron-rich partial negative ( opposite to pyridine ring)
N N
Hδ
δ
δ
δ-
-+
+
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Electrophilic Substitution on the Pyrrole Ring
• Because the ring carbon are the negative part the carbon are activated toward electrophilic
attack (pyrrole is more reactive than benzene)
N
H
SO3pyridine N
H
SO3H
N
H
HNO3
(CH3CO)2O N
H
NO2
2-pyrrolesulphonic acid
2-nitropyrrole
Substitution occurs at the 2-position
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Substitution at the 2-position is Favored over the 3-position
2-nitration
N
HNO2
H+
N
HNO2
H+
N
HNO2
H+
+NO2
N
H
N
H
NO2
-H+
3 resonance structures for the intermediate of nitration at the 2-position
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Nitration at the 3-position
+ +N
H
HNO2
N
H
HNO2
-H+
N
H
NO2
N
H
+NO2
The are only 2 resonance structures for the intermediate of nitration at the 3-position as compared to 3-resonance structures at the 2-position substitution at 2-position is favored.
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Other five-membered HetercyclicAromatic Compounds
• Furan and thiphene behave like pyrrole toward electrophilic substitution,
Br2
O OBr
SSO3H
H2SO4
SO3S
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Porphyrins• The porphyrin ring system is aromatic planar
compound contains four pyrrole rings joined by =CH- groups.
• They are biologically important unit.
The highlighted hydrogen atoms can be replaced by metal ions
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