Hydroperoxide: Difference between revisions
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[[Category:Chemical compounds]] | [[Category:Chemical compounds]] | ||
[[Category:Peroxides]] | [[Category:Peroxides]] | ||
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File:FunktionelleGruppen_Hydroperoxide.svg|Hydroperoxide functional group | |||
File:Sharpless_epoxidation_DE.svg|Sharpless epoxidation | |||
File:Hock-Phenol.png|Hock process for phenol | |||
File:Schenk-En-Reaktion.png|Schenk ene reaction | |||
File:Tetrahydrofuran_peroxide_formation.svg|Tetrahydrofuran peroxide formation | |||
File:LyaseNonenalHemiAc.png|Lyase nonenal hemiacetal | |||
File:Karen'sOOH.svg|Hydroperoxide | |||
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Latest revision as of 11:13, 18 February 2025

Hydroperoxide is a compound that contains the hydroperoxy functional group (composed of an oxygen-oxygen single bond attached to a hydrogen atom). This group is denoted as -OOH. Hydroperoxides are considered a type of peroxide, which is a broader category of compounds that contain an oxygen-oxygen bond. The presence of the hydrogen atom distinguishes hydroperoxides from other peroxides. Hydroperoxides play a significant role in various chemical processes, including organic synthesis, polymerization, and the degradation of materials. They are also pivotal in atmospheric chemistry and the initiation of combustion processes.
Formation[edit]
Hydroperoxides are typically formed through the reaction of oxygen (O2) with organic compounds, especially in the presence of light or certain catalysts. This process is known as autoxidation. In organic chemistry, the formation of hydroperoxides is often the first step in the autoxidation of alkenes, ethers, and other susceptible compounds. The reaction involves the formation of a radical intermediate, which then reacts with molecular oxygen to form the hydroperoxide.
Chemical Properties[edit]
Hydroperoxides are reactive species due to the weak O-O bond, which has a relatively low dissociation energy. This makes them prone to decomposition, especially upon heating or in the presence of metal catalysts, into various radicals and compounds, including alcohols, ketones, and aldehydes. The decomposition of hydroperoxides can be both a useful reaction in synthesis and a hazardous event, as it can lead to explosive outcomes under certain conditions.
Uses[edit]
In the chemical industry, hydroperoxides serve as initiators for polymerization reactions and as intermediates in the synthesis of fine chemicals. For example, cumene hydroperoxide is a key intermediate in the production of phenol and acetone via the cumene process. Hydroperoxides are also used in the formulation of various organic peroxides, which are essential in polymer chemistry.
Safety[edit]
Due to their instability and potential for explosive decomposition, hydroperoxides require careful handling and storage. Safety measures include the use of stabilizers, temperature control, and the avoidance of contact with incompatible materials such as strong acids, bases, and reducing agents.
Environmental Impact[edit]
Hydroperoxides play a crucial role in atmospheric chemistry, particularly in the formation of tropospheric ozone and other oxidants. They are involved in the oxidation of volatile organic compounds (VOCs), which contributes to air pollution and has implications for human health and climate change.
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Hydroperoxide functional group
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Sharpless epoxidation
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Hock process for phenol
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Schenk ene reaction
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Tetrahydrofuran peroxide formation
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Lyase nonenal hemiacetal
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Hydroperoxide