Sandrogreco Tautomeric Equilibria In Relation To Pi Electron Delocalization
Lecture 10 More Aromaticswillson.cm.utexas.edu/Teaching/Chemistry 328N 2019/Files... ·...
Transcript of Lecture 10 More Aromaticswillson.cm.utexas.edu/Teaching/Chemistry 328N 2019/Files... ·...
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Chemistry 328N
More AromaticsLecture 10
February 21, 2019
H
H
H
HH
H
H
H
H
H H
H
H
H
H
H
H
H
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Chemistry 328N
From Lecture 9
Erich Armand Arthur
Joseph Hückel
1896 - 1980
Arthur Atwater Frost
1909 - 2002
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Chemistry 328N
To be Aromatic …a compound must :
1. be Cyclic
2. have one P orbital on each atom in the ring
3. be planar or nearly so to give orbital overlap
4. have a closed loop of 4n+2 pi electrons in the
cyclic arrangement of p orbitals
Hückel's Rule for Aromaticity
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Chemistry 328N
Among planar, monocyclic, completely conjugated
polyenes, only those with 4n + 2p electrons possess
special stability (are aromatic)
n 4n+2
0 2
1 6 benzene!
2 10
3 14
4 18
Hückel's Rule
Magic Numbers
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Chemistry 328N
Actually and inadvertently defines a condition
for cyclic molecules in which the bonding
molecular orbitals are filled and there are no
electrons in non-bonding or antibonding
orbitals …. roughly analogous to the
“rare gas” condition for atomic orbitals…
Hückel's Rule
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Chemistry 328N
Benzene
Antibonding
Bonding
6 p electrons fill all of the bonding orbitals
all p antibonding orbitals are empty
p-MOs of Benzene
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Chemistry 328N
Hückel and Pyridine
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Chemistry 328N
Hückel and Pyrrole
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Chemistry 328N
Huckel and Furan
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Chemistry 328N
Recognizing Aromatic CompoundsBe careful with Huckel’s Rule
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Chemistry 328N
Some Nomenclature
A
B
A
B
A
B
Ortho
or 1,2Meta
or 1,3
Para
or 1,4
Please read about naming in Chapter 21!
http://www.word-origins.com/definition/benzene.html
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Chemistry 328N
Some Nomenclature
Please read about naming in Chapter 21.3. Many substituted benzenes
are so old and so common that they have been given “nick” names!
OH CH3 CH3
CH3
CH3
CH3
CH3
CH3
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Chemistry 328N
Benzene rings--substitution patterns
From Crewes, Rodriguez and Jaspars, ch 8Out-of-plane bending combinations,
quite small, but in a normally clean
region of IR. Reliable even with nitro or
carboxyl substitution
850,780,
700
R
R
R
R
R
R
R
750
750,700
820
Unreliable with NO2, CO2H subs
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Chemistry 328N
If the region between 1667-2000 cm-1 (w) is free of
interference (C=O stretching frequency) a weak
grouping of peaks is observed for aromatic systems.
Analysis of this region can lead to a determination of
the substitution pattern on the aromatic ring
Monosubstituted
1,2 disubstituted (ortho or o-)
1,2 disubstituted (meta or m-)
1,4 disubstituted (para or p-)
G
G
G
G
G
G
G
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Chemistry 328N
CH3
CH3
CH3
CH3
CH3
CH3
768 cm-1 691 cm-1
742 cm-
795 cm-1
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Chemistry 328N
Secondary magnetic field
generated by circulating pelectrons deshields aromatic
protons
Circulating p electrons
Ring Current in BenzeneRing Current in Benzene
Bo
Deshielded
H H
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Chemistry 328N
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Chemistry 328N
NMR Spectrum of Toluene
CH35
3
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Chemistry 328N
18 p electrons satisfies Hückel's rule
resonance energy = 418 kJ/mol
bond distances range between 137-143 pm
[18]Annulene
H HH
HH
H
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Chemistry 328N
nmr Spectroscopy
⚫ Ring Current effect is massive in the larger
annulenes, for example for [18]annulene
H
H
H
HH
H
H
H
H
H H
H
HH
HH
H
H
the six hydrogens on
the inside of the ring
resonate at d - 3.00!!
Up field of TMS!!
the twelve hydrogens on
the outside of the ring
resonate at d 9.3
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Chemistry 328N
Ortho H’s = 9 Hz
Meta H’s = 3 Hz
Para H’s < 1 Hz
Coupling Constants - Aromatics
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Chemistry 328N
NMR Spectrum of
1-iodo-4-methoxybenzene
OCH3I
CHCl3 impurity
2 2
3
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Chemistry 328N
NMR Spectrum of
1-bromo-4-ethoxybenzene
OCH2CH3Br
4
2
3
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Chemistry 328NX = Y X ~ X’ X = X
THE p-DISUBSTITUTED PATTERN CHANGES AS THE
TWO GROUPS BECOME MORE AND MORE SIMILAR
all H
equivalent
All peaks move closer.
Outer peaks get smaller …………………..… and finally disappear.
Inner peaks get taller…………………………. and finally merge.
X
X
X
X'
X
Y
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Chemistry 328N
Phenols⚫ The functional group of a phenol is an -OH
group bonded to a benzene ring
Phenol
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Chemistry 328N
Phenols
⚫ Cresols
Phenol o-cresol m-cresol p-cresol
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Chemistry 328N
La Brea Tar Pits
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Chemistry 328N
Phenol
Joseph Lister
1827 - 1909
A British surgeon and a pioneer of
antiseptic surgery, who successfully
introduced carbolic acid (now known as
phenol) to sterilize surgical instruments
and to clean wounds, which led to
reducing post-operative infections and
made surgery safer for patients.
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Chemistry 328N
Carbolic Acid Antiseptic
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Chemistry 328N
Acidity of Phenols
⚫ Phenols are much more acidic than aliphatic alcohols that also contain the -OH group
⚫ delocalization of the negative charge by resonance stabilizes the phenoxide ion relative to the alkoxide ion
Phenol: pKa = 9.95
Ethanol: pKa= 15.9
OH O-
CH3CH2O -
CH3CH2OH
H2O+
H2O+
H3O+
+
H3O+
+
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Chemistry 328N
Lets move electrons together!!
PLEASE FOLLOW ME STEP BY STEP
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Chemistry 328N
Acidity of Phenols
OH + OH- O- + H2 O
pKa 9.95pKa 15.7
Strong
acid
Strong
base
Weak
base
Weak
acid+ +
• Strong acids have weak conjugate bases
• Stabilization of anions leads to weak/stable conjugate bases!
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Chemistry 328N
Acidities of Phenols
– Part of the acid-strengthening effect of -NO2 is due to
its electron-withdrawing inductive effect
– In addition, -NO2 substituents in the ortho and para
positions help to delocalize the negative charge by
Resonance
••
+ +
delocalization of negative charge onto oxygen
O
O ON
O
O
NO
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Chemistry 328N
Acidities of Phenols
⚫ Nitro groups increase the acidity of phenols by
both an electron-withdrawing inductive effect and
a resonance effect
pKa 7.15pKa 8.28pKa 9.95p-Nitrophenolm-NitrophenolPhenol
OH
NO2
OH
NO2
OH
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Chemistry 328N
Acidity of Phenols
⚫ Alkyl and halogen substituents effect acidities by
inductive effects
– alkyl groups are electron-releasing by “induction”
– halogens are electron-withdrawing by “induction”
pKa 9.18pKa 8.85
m-Chloro phenolPhenol m-Cresol p-Cresol
pKa 9.95 pKa 10.01 pKa 10.17
OH
CH3
OH
CH3
OH OH
ClCl
OH
p-Chloro-phenol
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Chemistry 328N
Finally….Chemistry!!
A + B C
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Chemistry 328N
Synthesis: Alkyl-Aryl Ethers
⚫ Alkyl-aryl ethers can be prepared by the
Williamson ether synthesis
– but only using phenoxide salts and alkyl halides
– aryl halides are unreactive to SN2 reactions
no reaction+X RO-Na
+ X
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Chemistry 328N
Alkyl-Aryl Ethers
Sn2 reactions are accelerated by:
• polar aprotic solvents
• phase transfer catalysis
• crown ethers
Remember: methyl > 10 >20 and 30 is a no go!
{Review chapter 8??}
OO-
Cl
Cl-
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Chemistry 328N
Reactions at Benzyl Carbons
CH3
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Chemistry 328N
Benzylic Reactions
⚫ Benzylic radicals ( and cations) are easily formed because
of the resonance stabilization of these intermediates
– the benzyl radical is a hybrid of five contributing structures
C
H
H
.
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Chemistry 328N
Benzylic Bromination
⚫ Bromination proceeds by a radical mechanism
NBS
CCl4
Br
Slow
N OO
Br
N OO+ Br
NBS = N-bromosuccinimide
A Regioselective reaction ! !
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Chemistry 328N
Flash Card Tricks
⚫ frontBr
??
⚫ Back
NBS
CCl4
???
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Chemistry 328N
Allylic and benzylic
bromination with NBS