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Capítulo 8

Reacciones de los alquenos

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Regioselectividad de las adiciones electrofílicas - Efecto peróxido
Regioselectividad de las adiciones electrofílicas - Efecto peróxido
In the presence of organic peroxides, the addition of hydrogen bromide to an alkene yields the isomer that is not predicted by Markovnikov’s rule. ...

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Reacción en cadena de radicales libres y polimerización de alquenos
Reacción en cadena de radicales libres y polimerización de alquenos
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a ...

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Halogenación de alquenos
Halogenación de alquenos
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence ...

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Formación de halohidrina a partir de alquenos
Formación de halohidrina a partir de alquenos
An alkene, such as propene, reacts with bromine in the presence of water to yield a halohydrin. Halohydrins contain a halogen and a hydroxyl group ...

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Hidratación de alquenos catalizada por ácido
Hidratación de alquenos catalizada por ácido
Alkenes react with water in the presence of an acid to form an alcohol. In the absence of acid, hydration of alkenes does not occur at a significant rate, ...

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Regioselectividad y estereoquímica de la hidratación catalizada por ácido
Regioselectividad y estereoquímica de la hidratación catalizada por ácido
The rate of acid-catalyzed hydration of alkenes depends on the alkene's structure, as the presence of alkyl substituents at the double bond can ...

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Oximercuriación-Reducción de alquenos
Oximercuriación-Reducción de alquenos
Oxymercuration–reduction of alkenes is one of the major reactions converting alkenes to alcohols. It involves the hydration of alkenes with mercuric ...

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Hidroboración-Oxidación de Alquenos
Hidroboración-Oxidación de Alquenos
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary ...

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Regioselectividad y estereoquímica de la hidroboración
Regioselectividad y estereoquímica de la hidroboración
A significant aspect of hydroboration–oxidation is the regio- and stereochemical outcome of the reaction. Hydroboration proceeds in a concerted ...

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Oxidación de alquenos: Dihidroxilación syn con Tetraóxido de Osmio
Oxidación de alquenos: Dihidroxilación syn con Tetraóxido de Osmio
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double ...

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Oxidación de alquenos: Dihidroxilación syn con permanganato de potasio
Oxidación de alquenos: Dihidroxilación syn con permanganato de potasio
Alkenes can be dihydroxylated using potassium permanganate.  The method encompasses the reaction of an alkene with a cold, dilute solution of ...

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Oxidación de alquenos: Anti dihidroxilación con peroxiácidos
Oxidación de alquenos: Anti dihidroxilación con peroxiácidos
Diols are compounds with two hydroxyl groups. In addition to syn dihydroxylation, diols can also be synthesized through the process of anti ...

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Escisión oxidativa de los alquenos: Ozonólisis
Escisión oxidativa de los alquenos: Ozonólisis
In ozonolysis, ozone is used to cleave a carbon–carbon double bond to form aldehydes and ketones, or carboxylic acids, depending on the work-up. ...

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Reducción de alquenos: Hidrogenación catalítica
Reducción de alquenos: Hidrogenación catalítica
Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a ...

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Reducción de alquenos: Hidrogenación catalítica asimétrica
Reducción de alquenos: Hidrogenación catalítica asimétrica
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of ...
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