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- https://chem.libretexts.org/Courses/Chabot_College/Chem_12A%3A_Organic_Chemistry_Fall_2022/10%3A_Properties_and_Reactions_of_Alkenes/10.24%3A_Oxidative_Cleavage_of_AlkenesOxidative cleavage of alkenes can occur by several different pathways. The most common reagents and pathways are discussed in this section.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Alkenes/Reactivity_of_Alkenes/OzonolysisOzonolysis is a type of weak oxidative cleavage where we cleave alkenes (double bonds) into either ketones, aldehydes or carboxylic acid using ozone.
- https://chem.libretexts.org/Workbench/Chemistry_LHS_Bridge/13%3A_Alkenes/13.04%3A_Reactivity_of_Alkenes/13.4.17%3A_OzonolysisOzonolysis is a type of weak oxidative cleavage where we cleave alkenes (double bonds) into either ketones, aldehydes or carboxylic acid using ozone.
- https://chem.libretexts.org/Workbench/Chemistry_LHS_Bridge/13%3A_Alkenes/13.04%3A_Reactivity_of_Alkenes/13.4.18%3A_Ozonolysis_of_Alkenes_and_AlkynesOzonolysis is a method of oxidatively cleaving alkenes or alkynes using ozone (O3), a reactive allotrope of oxygen. The process allows for carbon-carbon double or triple bonds to be replaced by d...Ozonolysis is a method of oxidatively cleaving alkenes or alkynes using ozone (O3), a reactive allotrope of oxygen. The process allows for carbon-carbon double or triple bonds to be replaced by double bonds with oxygen. This reaction is often used to identify the structure of unknown alkenes by breaking them down into smaller, more easily identifiable pieces.
- https://chem.libretexts.org/Courses/University_of_Illinois_UrbanaChampaign/Chem_2363A_Fundamental_Organic_Chemistry_I_(Chan)/05%3A_Addition_Reactions_of_Alkenes/5.09%3A_Oxidative_Cleavage_of_AlkenesOxidative cleavage of alkenes can occur by several different pathways. The most common reagents and pathways are discussed in this section.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Alkenes/Reactivity_of_Alkenes/Ozonolysis_of_Alkenes_and_AlkynesOzonolysis is a method of oxidatively cleaving alkenes or alkynes using ozone (O3), a reactive allotrope of oxygen. The process allows for carbon-carbon double or triple bonds to be replaced by d...Ozonolysis is a method of oxidatively cleaving alkenes or alkynes using ozone (O3), a reactive allotrope of oxygen. The process allows for carbon-carbon double or triple bonds to be replaced by double bonds with oxygen. This reaction is often used to identify the structure of unknown alkenes by breaking them down into smaller, more easily identifiable pieces.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Basic_Principles_of_Organic_Chemistry_(Roberts_and_Caserio)/11%3A_Alkenes_and_Alkynes_II_-_Oxidation_and_Reduction_Reactions._Acidity_of_Alkynes/11.07%3A_Oxidation_ReactionsMost alkenes react readily with ozone, even at low temperatures, to yield cyclic peroxidic derivatives known as ozonides. Ozonization of alkenes has been studied extensively for many years, but there ...Most alkenes react readily with ozone, even at low temperatures, to yield cyclic peroxidic derivatives known as ozonides. Ozonization of alkenes has been studied extensively for many years, but there is still disagreement about the mechanism (or mechanisms) involved because some alkenes react with ozone to give oxidation products other than ozonides. Several oxidizing reagents react with alkenes under mild conditions to give, as the overall result, addition of hydrogen peroxide.
- https://chem.libretexts.org/Courses/Nassau_Community_College/Organic_Chemistry_I_and_II/08%3A_Reactions_of_Alkenes/8.15%3A_Oxidative_Cleavage_of_AlkenesOxidative cleavage of alkenes can occur by several different pathways. The most common reagents and pathways are discussed in this section.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Map%3A_Organic_Chemistry_(Wade)_Complete_and_Semesters_I_and_II/Map%3A_Organic_Chemistry_I_(Wade)/09%3A_Reactions_of_Alkenes/9.15%3A_Oxidative_Cleavage_of_AlkenesOxidative cleavage of alkenes can occur by several different pathways. The most common reagents and pathways are discussed in this section.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Map%3A_Organic_Chemistry_(Wade)_Complete_and_Semesters_I_and_II/Map%3A_Organic_Chemistry_(Wade)/09%3A_Reactions_of_Alkenes/9.15%3A_Oxidative_Cleavage_of_AlkenesOxidative cleavage of alkenes can occur by several different pathways. The most common reagents and pathways are discussed in this section.
- https://chem.libretexts.org/Courses/Westminster_College/CHE_261_-_Organic_Chemistry_I/09%3A_Electrophilic_Addition_Reactions_of_Alkenes_and_Alkynes/9.11%3A_More_Electrophilic_AdditionsMost alkenes react readily with ozone, even at low temperatures, to yield cyclic peroxidic derivatives known as ozonides. Ozonization of alkenes has been studied extensively for many years, but there ...Most alkenes react readily with ozone, even at low temperatures, to yield cyclic peroxidic derivatives known as ozonides. Ozonization of alkenes has been studied extensively for many years, but there is still disagreement about the mechanism (or mechanisms) involved because some alkenes react with ozone to give oxidation products other than ozonides. Several oxidizing reagents react with alkenes under mild conditions to give, as the overall result, addition of hydrogen peroxide.
