alquenosreacciones
TRANSCRIPT
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Reacciones de Alquenos:
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Introduction: Additions to Alkenes
Generally the reaction is exothermic because one and one bond
are converted to two bonds
The electrons of the double bond are loosely held and are a source
of electron density, i.e. they are nucleophilic
Alkenes react with electrophiles such as H+ from a hydrogen
halide to form a carbocation
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3
The carbocation produced is an electrophile
It can react with a nucleophile such as a halide
Insert top scheme pg 331
In addition reactions the alkene changes from a
nucleophile in the first step to an electrophile in the
second
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Electron-rich atoms or molecules (nucleophiles) are
attracted to electron-deficient atoms or molecules
(electrophiles)
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Addition Reactions
The pi ( ) bond is easily broken, which
makes double and
triple bonds very
reactive.
In the addition reaction, reactants
are added to the
carbon atoms in the
double or triple bond.
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Reacciones de Alquenos
Alkenes react with many electrophiles to give useful
products by addition (often through special reagents)
Haluros (adicion H-X)
alcoholes (adicion H-OH)
dihaluros (adicion X-X)
alkanes (adicion H-H)
halohidrinas (adicion HO-X)
dioles (adicion HO-OH)
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REACCIONES DE ADICION
Son caractersticas de los compuestos insaturados: alquenos y alquinos
Reaccin de adicin a un alqueno se rompe el enlace y el par de e- se usa en la formacin de dos nuevos
enlaces
C C
sp2 sp3
YZ Y Z
Se combinan dos molculas para dar una sola
Inversa de la eliminacin
Nube de electrones disponibles para electrfilos
ADICION ELECTROFILICA C C
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Electrophilic Addition of HX to Alkenes
General reaction mechanism: electrophilic addition
Attack of electrophile (such as HBr) on bond of alkene produces carbocation
and bromide ion
Carbocation is itself an electrophile, reacting with nucleophilic bromide ion
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Writing Organic Reactions
No established convention shorthand
Can be formal kinetic expression
Not necessarily balanced
Reactants can be before or on arrow
Solvent, temperature, details, on arrow
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Curved Arrows in Reaction Mechanisms
Movement of a pair of electrons
Movement of one electron
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Curved Arrows Show the Flow of
Electrons
electron-rich center
electron-deficient center
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Rules on Using Curved Arrows
1. Arrows are drawn in the direction of the electron flow
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2. Curved arrows indicate the movement of electrons
3. The head of a curved arrow always points at an atom
CH3COCH3
O
HO -
+ CH3COCH3
O -
OH
CH3COCH3
O
HO -
+ CH3COCH3
O -
OH
correct incorrect
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4. The arrow starts at the electron source
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REACCIONES DE ADICION ELECTROFILICA
C C
Hidratacin C C
H OH
Halgenos
C C
Cl Cl
Hidroxilacin
C C
OH OH
Hidrogenacion
C C
H H
Halohidrinas
C C
Cl OH
Halogenuros de hidrgeno
C C
H Cl
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Electrophilic Addition of HX to
Alkenes
General reaction mechanism: electrophilic
addition
Attack of electrophile (such as HBr) on
bond of alkene produces carbocation and
bromide ion
Carbocation is itself an electrophile,
reacting with nucleophilic bromide ion
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In hydrohalogenation, the atoms of a hydrogen
halide add to the carbon atoms of a double
bond or triple bond.
Hydrohalogenation
CH3 CH CH CH3
H Cl
+ HClCH3 CH CH CH3
H
Br
+ HBr
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When an unsymmetrical alkene undergoes hydrohalogenation, the H in HX adds to the carbon in the double bond that has the greater number of H.
Markovnikovs Rule
CH3 CH CH2
Cl H
CH3 CH CH2 + HCl
CH3 CH CH2
H Cl
Does not form
C with the most H
Product that forms
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ADICION DE HALUROS DE HIDROGENO
CH2=CH2 + HX CH3CH2X
CH CH CH2=CHX CH3CHX2 HX HX
MECANISMO
CH3CH=CH2
H Cl
Paso 1 (lento)
Paso 2 (rpido)
CH3CH CH2
H
intermediario carbocatin
+ Cl-
CH3CH CH2
HCl-
CH3CHClCH3
- +
Reactivo: HBr (g) , HCl (g)
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CH3CH=CH2 CH3CHClCH3
HCl
CH3CH2CH2Cl
REGIOSELECTIVIDAD DE LA ADICIN DE HX A ALQUENOS
Regla de Markovnikov
En la adicin de HX a alquenos no
simtricos, el H+ de HX se dirige al
carbono con > nmero de hidrgenos
CH3CH=CH2
H Cl
CH3CH CH2
H Se va a formar el carbocatin ms estable que es el ms
sustituido
ORDEN DE ESTABILIDAD DE CARBOCATIONES
< < < <
ESTABILIDAD
CH3+
metilo
CH2CH3+
primario
(CH3)2CH+
secundario
(CH3)3C+
terciario
CH2=CH-CH2+
allico
benclico
CH2+
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Two step
process
First transition
state is high
energy point
Electrophilic Addition Energy
Diagram:
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Stability of Carbocations and
Markovnikovs Rule More stable carbocation forms faster
Tertiary cations and associated transition states are more stable
than primary cations
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Example of Electrophilic
Addition
Addition of hydrogen
bromide to 2-Methyl-
propene
H-Br transfers proton to
C=C
Forms carbocation
intermediate
More stable cation
forms
Bromide adds to
carbocation
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Electrophilic Addition for Syntheses
The reaction is successful with HCl and with HI as well
as HBr. Note that HI is generated from KI and
phosphoric acid
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Orientacion de la adicion electrofilica:
Regla de Markovnikov En un alqueno asimetrico, el reactivo HX puede
adicionarse de dos maneras distintas, pero una es preferida sobre la otra.
Si una orientacion predomina, se dice que la reaccion es regiospecifica
Markovnikov observo en el siglo XIX que en la adicion de HX a un alqueno, el H se une al carbono con mas hidrogenos y el X se une al otro carbono (aquel con mayor numero de sustituyentes alquilicos)
Esta es la Regla de Markovnikov
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Addition of HCl to 2-methylpropene is regiospecific one product forms where two are possible
If both ends have similar substitution, then the reaction is not regiospecific
Example of Markovnikovs Rule
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Same example:
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Practice Problem:
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Solution:
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Practice Problem:
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Solution:
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Problem : Major products?
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Problem : Which alkene?
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Mecanismo adicion electrofilica de alquenos
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Transition State resembles cation
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a more stable
carbocation
Carbocation Formation Is the Rate-
Limiting Step
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Carbocation Stabilities
Alkyl groups decrease the concentration of positive
charge in the carbocation
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Carbocation Structure and Stability
Carbocations are planar
The positively charged carbon is
surrounded by only 6 electrons in
three sp2 orbitals
The fourth orbital on carbon is a
vacant p-orbital
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Carbocation Structure and Stability
The stability of the carbocation
(measured by energy needed to form it
from R-X) is increased by the presence
of alkyl substituents
Therefore stability of carbocations:
3 > 2 > 1 > +CH3
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Heterolytic bond dissociations
energies:
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Stabilizing Carbocations:
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Electrophilic Addition Reactions Are
Regioselective
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Mechanism of Electrophilic Addition:
Rearrangements of Carbocations
Carbocations undergo structural
rearrangements following set patterns
1,2-H and 1,2-alkyl shifts occur
Goes to give more stable carbocation
Can go through less stable ions as
intermediates
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Rearrangement of Carbocation
1,2-hydride shift a more stable carbocation
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a more stable
carbocation
Rearrangement of Carbocation
1,2-methyl shift
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Carbocation does not always rearrange
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Carbocation Rearrangement
a more stable
carbocation
Ring Expansion
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Carbocation rearrangements:
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Hydride Shifts
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Alkyl (methyl) shifts
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TRANSPOSICIONES
CH3 C CH CH2
CH3
H
CH3 C CH CH3
CH3
H
+ CH3 C CH CH3
CH3
H OH
CH3 C CH CH3
CH3
H+
transposicin de hidruro
CH3 C CH CH3
CH3
HOH
El desplazamiento 1,2 de hidruro convierte al carbocatin secundario en uno
terciario que es ms estable produciendo el alcohol terciario como producto
mayoritario
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Problem : mechanism?
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H
Br
HBr
H-shift
Br-1
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Problem : mechanism?
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CH3
H3C
CH2
CH3
H3C
CH3
CH3
CH3
CH3
CH3
CH3
CH3
Cl
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Problem : What will be the
rearranged cations?
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Problem : mechanism?
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Problem : carbocation structure?
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ADICION DE HBr ANTI-MARKOVNIKOV
CH3CH=CH2
HBr
CH3CH2CH2Br perxidos
MECANISMO RADICALES
1. Formacin del radical Br
ROOR 2 RO
RO + HBr ROH + Br
2. Adicin de Br al alqueno
Br + CH3CH=CH2 CH3CHBrCH2 CH3CHCH2Br
3. Formacin del producto
CH3CHCH2Br
+ H-Br CH3CH2CH2Br + Br
C-O
O
O-C
O
C-O
O
35 kcal/mol
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In hydration, H and OH from water add to the
carbon atoms of a double bond or triple bond
to form alcohols (OH).
The reaction is catalyzed by acid H+.
Hidratacion de alquenos: Alcoholes
+ HOHH
OH
CH3 CH CH2 + HOH
CH3 CH CH2
OH H
H+
H+
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Addition of Water to Alkenes:
Hydration
Hydration of an alkene is the addition of H-OH
to to give an alcohol
Acid catalysts are used in high temperature
industrial processes: ethylene is converted to
ethanol
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Addition of HOH to Alkene
What is the electrophile?
What nucleophile is present in the greatest concentration?
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HIDRATACION
CH3CH=CH2 + H2O CH3CH CH3
OHH+
MECANISMO 2 pasos como adicin de HX
1.
CH3CH CH2
H
CH3CH=CH2 + H+
CH3CH CH2
H
+ H2O CH3CH CH3
OH2
+
- H+ CH3CH CH3
OH
Sigue la regla de
Markovnikov produciendo
el alcohol ms sustituido
Es la inversa de la
deshidratacin de
alcoholes E1
Catlisis cida
ALQUINOS
CH3CH2C CH + H2O HgSO4
H2SO4 CH3CH2C CH2
OH
CH3CH2C CH3
O
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Francis A. Carey, Organic Chemistry, Fourth Edition. Copyright 2000 The McGraw-Hill Companies, Inc. All rights reserved.
Mechanism of acid-catalyzed hydration
of 2-methylpropeneFigure 6.9
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Addition of Water to Alkenes:
Hydroboration
Herbert Brown (HB) invented hydroboration (HB)
Borane (BH3) is electron deficient: a Lewis acid
Borane adds to an alkene to give an organoborane
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BH3 is a Lewis Acid
Six electrons in outer shell
Coordinates to oxygen electron pairs in ethers
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Addition of H-BH2 (from BH3-THF complex) to three alkenes gives a trialkylborane
Oxidation with alkaline hydrogen peroxide in water produces the alcohol derived from the alkene
Hydroboration-Oxidation Forms an
Alcohol from an Alkene
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Orientation in Hydration via
Hydroboration Regiochemistry is opposite to Markovnikov
orientation (anti Markovnikov )
OH is added to carbon with most Hs
H and OH add with syn stereochemistry, to the same face of the alkene (opposite of anti addition)
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Mechanism of
Hydroboration Borane is a Lewis acid
Alkene is Lewis base
Transition state involves
anionic development on B
The components of BH3
are across C=C
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Hydroboration: Orientation in
Addition Step
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Hydroboration, Electronic Effects Give
anti-Markovnikov
More stable carbocation is also consistent with steric
preferences
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Steric Preference
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Hydroboration - Oxygen
Insertion Step
H2O2, OH- inserts OH in place of B
Retains syn orientation
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HIDRATACION ANTI-MARKOVNIKOV HIDROBORACION-OXIDACION
CH3CH=CH2 1.BH3
2. H2O2, OH-
CH3CH2CH2OH
B2H6
(CH3CH2O)2O
2 BH3
gas txico
MECANISMO
CH3 CH CH2
H BH2- +
CH3 CH CH2
H BH2
hidrgeno en el carbono
ms sustituido
CH2=CH2 BH2CH2CH3
CH2=CH2 BH(CH2CH3)2
CH2=CH2
B(CH2CH3)3 H2O2, OH
- CH3CH2OH
CH3 CH CH2
H OH
alcohol menos sustituido
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ESTEREOQUMICA DE LA HIDROBORACIN
CH3H
H2O2/ HO-
CH3
OHH
H
CH3H
OH H
HBH2
H
CH3H
BH2
ADICION SYN
El tomo de boro y el hidruro se adicionan a los dos
tomos del doble enlace simultneamente
Ambos se adicionan del mismo lado del doble enlace
Cuando el organoborano se oxida al alcohol el grupo OH- ocupa la posicin del boro
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Hidrogenacion alquenos
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In hydrogenation, hydrogen atoms add to the carbon atoms of a double bond or triple bond.
A catalyst such as Pt or Ni is used to speed up the reaction.
Hydrogenation
HC CH + 2H2Ni
HC CH
H H
H H
H2C CH2
H HPt
H2H2C CH2 +
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HIDROGENACION CATALITICA
CH3CH=CH2 H2 / Pt
CH3CH2CH3
CH3C CCH3 H2 / Pt CH3CH2CH2CH3
H2 / Pd Na2CO3
Pb(AcO)4 quinolina
C C
H3C CH3
H H
Na / NH3 (lq)
cis
CH3
H
C C
H3C
H
trans
CATALIZADOR
Metal finamente dividido
o adsorbido sobre un
soporte insoluble e
inerte como carbono
o carbonato de bario
Para reducir alquenos
Pt Pd Ni Cu
Catalizador envenenado
es aquel que est
parcialmente desactivado
por tratamiento del metal
(Lindlar)
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progreso de la reaccin
E
CH3CH=CH2
CH3CHCH3 +
CH3CH2CH2+
DIAGRAMA DE ENERGA PARA LA PROTONACION DEL PROPENO
Ea2
Ea1
Ea2 < Ea1
carbocatin secundario
Efecto inductivo
Desplazamiento de electrones a travs de
enlaces debido a la diferencia de electro-
negatividad entre los tomos de un enlace
H C+ C
R
R
R
120
C+
Hiperconjugacin
Superposicin del orbital p vaco del
sp2 con el orbital de un enlace C-H vecino
Los e- del enlace estabilizan la carga positiva del carbocacin dispersndola
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MECANISMO
H H R2C=CR2 C C
R
R R
RH H
C C
R
R R
R
H H H
C C
R
R R
R
H
Primero el H2 se adsorbe sobre la superficie del metal, luego se rompen los
enlaces y se forman enlaces H-metal. Se adsorbe el alqueno en la superficie
del metal y su orbital interactua con los orbitales vacos del metal
La molcula de alqueno se desplaza sobre la superficie hasta que colisiona con
un tomo de hidrgeno unido al metal, se produce la reaccin y se regenera
el catalizador
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Mechanism of Catalytic
Hydrogenation
Heterogeneous reaction between phases
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Catalytic Hydrogenation of an Alkene
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Hydrogenation
Alkene + H2 Alkane
Catalyst required, usually Pt, Pd, or Ni.
Finely divided metal, heterogeneous
Syn addition
=>
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ESTEREOQUIMICA DE LA HIDROGENACION CATALITICA
ADICION SYN Los dos tomos de hidrgeno se adicionan a la misma cara
del doble enlace
H
H
H
H
CH3
CH3
CH3
CH3
CH3H3C
H3C
H
CH3H3C
H
CH3H2
Pd
H2
PtO2
- pineno reduccin exclusivamente en la
cara inferior por bloqueo del metilo
cis-1,2-dimetilciclohexano
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Reduction of Alkenes:
Hydrogenation
Requires Pt or Pd as powders on carbon and H2 Hydrogen is first adsorbed on catalyst
Reaction is heterogeneous (process is not in solution)
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Syn Addition
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Steric effect:
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Hydrogen Addition- Selectivity
With Pt or Pd catalysts, selective for C=C.
No reaction with C=O, C=N
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Hydrogen Addition- Selectivity
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Problem : Major Products?
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Solid Fats from Liquid Oils
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100
When hydrogen adds to the
double bonds in
vegetable oils, the
products are
solids at room
temperature.
Hydrogenation of Oils
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In halogenation, halogen atoms add to the
carbon atoms of a double bond or triple
bond.
Halogenation
+ HC C CH3 2Cl2C C
Cl Cl
Cl Cl
CH3H
H2C CH2
Br Br
Br2H2C CH2 +
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Testing for Double and Triple
Bonds
When bromine (Br2) is
added to an alkane, the
red color of bromine
persists.
When bromine (Br2) is
added to an alkene or
alkyne, the red color of
bromine disappears
immediately.
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Fin hidrogenacion alkenes
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Addition of Halogens to Alkenes
Bromine and chlorine add to alkenes to give 1,2-
dihaldes, an industrially important process
F2 is too reactive and I2 too unreactive
Cl2 reacts as Cl+ Cl-; Br2 is similar
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Addition of Br2 to Cyclopentene
Addition is exclusively trans (stereospecific)
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Mechanism of Bromine Addition
Br+ adds to an alkene producing a cyclic cation: a bromonium ion, in which bromine shares charge with carbon
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Mechanism of Bromine Addition
Since the Br blocks one face, one must get anti (trans) addition
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Addition of Br2 to Cyclopentene
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The Reality of Bromonium Ions Bromonium were postulated more than 60 years ago to explain
the stereochemical course of the addition (to give the trans-dibromide from a cyclic alkene
George Olah (Nobel Prize 1994) showed that bromonium ions are stable in liquid SO2 with SbF5 and can be studied directly by nuclear magnetic resonance spectroscopy
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111
Halohydrin Formation
This is formally the addition of HO-X to an
alkene (with +OH as the electrophile) to give a
1,2-halo alcohol, called a halohydrin
The actual reagent is the dihalogen (Br2 or Cl2
with water in an organic solvent)
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Mechanism of Formation of a
Bromohydrin
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113
Mechanism of Formation of a
Bromohydrin
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114
Mechanism of Formation of a
Bromohydrin
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115
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116
An Alternative to Bromine
Bromine is a difficult reagent to use for this reaction
N-Bromosuccinimide (NBS) produces bromine in organic solvents and is a safer source
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MECANISMO
CH3CH CH2
BrBr
- Br -
bromonio asimtrico
CH3CH CH2
Br
+
Br - bromuro ataca del lado opuesto
al que est el bromo ADICION ANTI
Br H
H
CH3C CH
Br
EVIDENCIA DE ADICION ANTI
H
H
Br
Br
H
H
Br
HH +
Br-
Br- Br
Br
H
H + trans
cis
Br2
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FORMACION DE HALOHIDRINAS
R2C=CH2
X2, H2O
OH
R2C CH2
Br
1,2-halohidrina
X: Cl o Br
MECANISMO
CH3CH CH2
BrBr
- Br - CH3CH CH2
Br
+
H2O
OH
CH3C CH2
BrH
OH2
CH3C CH2
BrH
+
-H+
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119
ADICION DE HALOGENOS
Br2 CH3CH CHCH3
CH3C CCH3
Br
CH3CH CHCH3
Br
Br Br
Br
CH3C CCH3
BrBr2
Bromo y cloro se
adicionan al doble
o triple enlace
Fluor da reacciones
explosivas
Iodo se adiciona pero
el producto es inestable
CH2=CH2 < RCH=CH2 < R2C=CH2 < R2C=CHR < R2C=CR2
ORDEN DE REACTIVIDAD DE LOS ALQUENOS
REACTIVIDAD
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OxidationofAlkenes:Hydroxylation
HydroxylationaddsOHtoeachendofC=C Oxidizingagentisosmiumtetroxide Stereochemistryofadditionissyn Productisa1,2dialcoholordiol (alsocalleda
glycol)
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OXIDACIONDEALQUENOS
Variosproductosdependiendodelalquenoydeloxidante
OXIDACIONDELENLACE SINRUPTURADELENLACEOXIDACIONDELENLACE CONRUPTURADELENLACE
OXIDACIONSINRUPTURA FORMACIONDEDIOLES
OHOH
HHO
O
HH
O-
O
Mn
OO
HH
O
O
Os
H
H
KMnO4,aq
25C
OsO4
Na2SO3
H2O
HO
cis1,2ciclohexanodiol
ADICIONSYN
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FormationofDiolsviaOsmiumTetroxide
Hydroxylation convertstosyndiol Osmiumtetroxide,thensodiumbisulfate Viacyclicosmatediester
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Problem:WhichAlkene?
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OXIDACIONCONRUPTURA OZONOLISIS
OO O- +
OO O-
+O
O O-+ O
O O-+
Ozono:molculaformadaportrestomosdeoxgeno
Oznolisis1.oxidacindelalquenoporozonoparadarunoznido
2.oxidacinoreduccindeloznido
Resultadodelaoznolisiseslarupturadeldobleenlacedelalquenoparaformardoscompuestoscarbonlicos,unoacadaladodledobleenlaceoriginal
C C C C+
Esunareaccindedegradacinyseusaparalocalizarlaposicindeundobleenlaceydeducirlaestructuradeunalquenodesconocido
Reactivo
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OzonolysisofAlkenes CleavageofalkeneswithozoneandworkupwithzincinaceticacidleadstolesshighlyoxidizedcarbonsthanproductsfromcleavagewithhotKMnO4
Unsubstitutedcarbonsareoxidizedtoformaldehyde,monosubstitutedcarbonsareoxidizedtoaldehydesanddisubstitutedcarbonsareoxidizedtoketones
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Ozoneaddsacrossthedoublebondtoformtheinitialozonidewhichrearrangestoahighlyunstableozonide
Theozonidesreactwithzincandaceticacidtoeffectthecleavage
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C CH3C CH3
H CH3
O O
OREDUCTIVA
aldehdocetona
+Zn/AcOH
OXIDATIVA
cido
2.Oxidacinoreduccindeloznido
H2O2 /H+ +
CH3CH
O
acetaldehdo
CH3CCH3
O
acetona
CH3CCH3
O
acetona
CH3COH
O
cidoactico
1.Oxidacindelalqueno
H
O
CH3-C C-CH3CH3
O OC C
H3C CH3
H CH3
O O
O
C CH3C CH3
H CH3
1,2,3trioxolano1,2,4trioxolano
OZONIDO
O3
CCl4
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OzonolysisofAlkenes CleavageofalkeneswithozoneandworkupwithzincinaceticacidleadstolesshighlyoxidizedcarbonsthanproductsfromcleavagewithhotKMnO4
Unsubstitutedcarbonsareoxidizedtoformaldehyde,monosubstitutedcarbonsareoxidizedtoaldehydesanddisubstitutedcarbonsareoxidizedtoketones
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SolvedProblem AnunknownalkenewithformulaC7H12 yieldsonlythefollowingproductonoxidationwithhotKMnO4
Answer:Sincenocarbonsaremissingintheproduct,thealkenemustbepartofaringintheoriginalmolecule
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AdditionofRadicalstoAlkenes:Polymers
Apolymer isaverylargemoleculeconsistingofrepeatingunitsofsimplermolecules(monomers),formedbypolymerization
Alkenesreactwithradicalcatalyststoundergoradicalpolymerization
Ethyleneispolymerizedtopolyethylene
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FreeRadicalPolymerizationofAlkenes
Alkenescombinemanytimestogivepolymer Reactivityinducedbyformationoffreeradicals
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FreeRadicalPolymerization:Initiation
Initiation afewradicalsaregeneratedbythehomolysisoftheOObondinbenzoylperoxide
Thebenzoyloxyradicaladdstoethylenetoformacarbonradical
-
Polymerization:Propagation
Radicalfrominitiationaddstoalkenetogeneratealkenederivedradical
Thisradicaladdstoanotheralkene,andsoonmanytimes
-
Polymerization:Termination
Chainpropagationendswhentworadicalchainscombine,orreactwithsomeradicalscavenger
Notcontrolledspecificallybutaffectedbyreactivityandconcentration
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OtherPolymers
-
UnsymmetricalMonomers
Ifthedoublebondisunsymmetrical,thereactionisviamorehighlysubstituted(morestable)radical
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ChainBranchingDuringPolymerization
Duringradicalpropagationchaincandevelopforksleadingtobranching
Onemechanismofbranchingisshortchainbranchinginwhichaninternalhydrogenisabstracted
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LongChainBranching
Inlongchains,ahydrogenfromanotherchainisabstracted
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CationicPolymerization
VinylmonomersreactwithBrnstedorLewisacidtoproduceareactivecarbocationthataddstoalkenesandpropagatesvialengtheningcarbocations
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Monomers
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NaturalRubber:
Madefromthesapofanumberofplants,principallyHeveabrasiliensis
Cruderubber(latex)isZpolyisoprene
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Alkenesobtention:EliminationReactions:
Alkenes are commonly made by elimination of HX from alkyl halide: (dehydrohalogenation); using heat and KOH and dehydration from alcohols.
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Francis A. Carey, Organic Chemistry, Fourth Edition. Copyright 2000 The McGraw-Hill Companies, Inc. All rights reserved.
Elimination by the E1 mechanismFigure 5.12
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ZaitsevsRule:FormationoftheMostSubstitutedAlkeneisFavoredwithaSmallBase
Somehydrogenhalidescaneliminatetogivetwodifferentalkeneproducts
ZaitzevsRule:whentwodifferentalkeneproductsarepossibleinanelimination,themosthighlysubstituted(moststable)alkenewillbethemajorproduct
Thisistrueonlyifasmallbasesuchasethoxideisused
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Heatsofhydrogenationofthreebuteneisomers:
OverallRelativeStabilitiesofAlkenes Thegreaterthenumberofattachedalkylgroups(i.e.themorehighlysubstitutedthecarbonatomsofthedoublebond),thegreaterthealkenesstability
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SynthesisofAlkenesviaEliminationReactions Dehydrohalogenation
ReactionsbyanE2mechanismaremostuseful E1reactionscanbeproblematic
E2reactionarefavoredby: Secondaryortertiaryalkylhalides Alkoxidebasessuchassodiumethoxideorpotassiumtertbutoxide
BulkybasessuchaspotassiumtertbutoxideshouldbeusedforE2reactionsofprimaryalkylhalides
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FormationoftheLeastSubstitutedAlkeneUsingaBulkyBase
Bulkybasessuchaspotassiumtertbutoxidehavedifficultyremovingstericallyhinderedhydrogensandgenerallyonlyreactwithmoreaccessiblehydrogens(e.g.primaryhydrogens)
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AcidCatalyzedDehydrationofAlcohols
Recallthateliminationisfavoredoversubstitutionathighertemperatures
Typicalacidsusedindehydrationaresulfuricacidandphosphoricacid Thetemperatureandconcentrationofacidrequiredtodehydrate
dependsonthestructureofthealcohol
Primaryalcoholsaremostdifficulttodehydrate,tertiaryaretheeasiest
Rearrangementsofthecarbonskeletoncanoccur
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MechanismforDehydrationofSecondaryandTertiaryAlcohols:AnE1Reaction
Onlyacatalyticamountofacidisrequiredsinceitisregeneratedinthefinalstepofthereaction
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Francis A. Carey, Organic Chemistry, Fourth Edition. Copyright 2000 The McGraw-Hill Companies, Inc. All rights reserved.
Mechanism of acid-catalyzed dehydration of tert-butyl alcoholFigure 5.6
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CarbocationStabilityandtheTransitionState Recallthestabilityofcarbocationsis:
ThesecondstepoftheE1mechanisminwhichthecarbocationformsisratedetermining
Thetransitionstateforthisreactionhascarbocationcharacter Tertiaryalcoholsreactthefastestbecausetheyhavethemoststabletertiarycarbocationliketransitionstateinthesecondstep
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TherelativeheightsofG forthesecondstepofE1dehydrationindicatethatprimaryalcoholshaveaprohibitivelylargeenergybarrier
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CarbocationStabilityandtheOccurrenceofMolecularRearrangements RearrangementsDuringDehydrationofSecondaryAlcohols
Rearrangementsofcarbocationsoccurifamorestablecarbocationcanbeobtained
Example
ThefirsttwostepsaretosameasforanyE1dehydration
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Francis A. Carey, Organic Chemistry, Fourth Edition. Copyright 2000 The McGraw-Hill Companies, Inc. All rights reserved.
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Prob.:Howmanyalkeneproductsfromdehydration?
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Solution:
AlquenosReaccionesIAlkenescontOxidation of Alkenes: HydroxylationSlide Number 2Formation of Diols via Osmium TetroxideProblem : Which Alkene?Slide Number 5Slide Number 6Slide Number 7Slide Number 8Slide Number 9Slide Number 10Addition of Radicals to Alkenes: PolymersFree Radical Polymerization of AlkenesFree Radical Polymerization: InitiationPolymerization: PropagationPolymerization: TerminationOther PolymersUnsymmetrical MonomersChain Branching During PolymerizationLong Chain BranchingCationic PolymerizationSlide Number 21MonomersNatural Rubber:Alkenes obtention: Elimination Reactions:Slide Number 25Slide Number 26Slide Number 27Slide Number 28Slide Number 29Slide Number 30Slide Number 31Slide Number 32Slide Number 33Slide Number 34Slide Number 35Slide Number 36Prob. : How many alkene products from dehydration?Solution: