Hydroperoxide

The bond length in peroxides is about 1.45 Å, and the angles (R = H, C) are about 110° (water-like). Characteristically, the dihedral angles are about 120°. The bond is relatively weak, with a bond dissociation energy of , less than half the strengths of , , and bonds. Hydroperoxides are typically more volatile than the corresponding alcohols: • tert-BuOOH (b.p. 36°C) vs tert-BuOH (b.p. 82-83°C) • Methyl hydroperoxide| (b.p. 46°C) vs Methanol| (b.p. 65°C) • cumene hydroperoxide (b.p. 153°C) vs cumyl alcohol (b.p. 202°C) • Triphenylmethyl hydroperoxide| (m.p. 87.5–88.5 °C) is a particularly stable example of a hydroperoxide ==Miscellaneous reactions==

Hydroperoxides are mildly acidic. The range is indicated by 11.5 for Methyl hydroperoxide| to 13.1 for . Hydroperoxides can be reduced to alcohols with lithium aluminium hydride, as described in this idealized equation: : This reaction is the basis of methods for analysis of organic peroxides. Another way to evaluate the content of peracids and peroxides is the volumetric titration with alkoxides such as sodium ethoxide. The phosphite esters and tertiary phosphines also effect reduction: : ==Uses==

Precursors to epoxides "The single most important synthetic application of alkyl hydroperoxides is without doubt the metal-catalysed epoxidation of alkenes." In the Halcon process tert-butyl hydroperoxide (TBHP) is employed for the production of propylene oxide. Of specialized interest, chiral epoxides are prepared using hydroperoxides as reagents in the Sharpless epoxidation. Production of cyclohexanone and caprolactone Hydroperoxides are intermediates in the production of many organic compounds in industry. For example, the cobalt catalyzed oxidation of cyclohexane to cyclohexanone: : Drying oils, as found in many paints and varnishes, function via the formation of hydroperoxides. Hock processes Compounds with allylic and benzylic C−H bonds are especially susceptible to oxygenation. Such reactivity is exploited industrially on a large scale for the production of phenol by the Cumene process or Hock process for its cumene and cumene hydroperoxide intermediates. Such reactions rely on radical initiators that reacts with oxygen to form an intermediate that abstracts a hydrogen atom from a weak C-H bond. The resulting radical binds , to give hydroperoxyl (ROO•), which then continues the cycle of H-atom abstraction. ==Formation==

By autoxidation The most important (in a commercial sense) peroxides are produced by autoxidation, the direct reaction of with a hydrocarbon. Autoxidation is a radical reaction that begins with the abstraction of an H atom from a relatively weak C-H bond. Important compounds made in this way include tert-butyl hydroperoxide, cumene hydroperoxide and ethylbenzene hydroperoxide: : : Auto-oxidation reaction is also observed with common ethers, such as diethyl ether, diisopropyl ether, tetrahydrofuran, and 1,4-dioxane. An illustrative product is diethyl ether peroxide. Such compounds can result in a serious explosion when distilled. : From hydrogen peroxide Many industrial peroxides are produced using hydrogen peroxide. Reactions with aldehydes and ketones yield a series of compounds depending on conditions. Specific reactions include addition of hydrogen peroxide across the C=O double bond: : In some cases, these hydroperoxides convert to give cyclic diperoxides: : Addition of this initial adduct to a second equivalent of the carbonyl: : Further replacement of alcohol groups: : Triphenylmethanol reacts with hydrogen peroxide in the presence of acid to give the hydroperoxide: : Naturally occurring hydroperoxides Many hydroperoxides are derived from fatty acids, steroids, and terpenes. The biosynthesis of these species is affected extensively by enzymes. is generated by conversion of linolenic acid to the hydroperoxide by the action of a lipoxygenase followed by the lyase-induced formation of the hemiacetal. In the remote troposphere, hydrogen peroxide (H₂O₂) and methyl hydroperoxide (CH₃OOH) are among the most abundant hydroperoxides and act as reservoirs for HOx (OH + HO₂), buffering radical concentrations and tracing oxidation chemistry. Formation in the remote troposphere is dominated by peroxy-radical chemistry: HO₂ + HO₂ → H₂O₂ + O₂ and CH₃O₂ + HO₂ → CH₃OOH + O₂ Global aircraft observations during NASA's Atmospheric Tomography (ATom) mission show that their distributions reflect formation via peroxy-radical chemistry and are modulated by season and recent convection. Under atmospheric conditions, the reaction of organic peroxyl radicals (RO₂) with HO₂—an important source of ROOH—exhibits a generally negative temperature dependence, and its product branching competes with RO₂ autoxidation (isomerization) and RO₂+RO₂ channels. Many functionalized RO₂ types (for example, β-hydroxy or highly oxygenated RO₂) still lack good laboratory data on rates and products. Because of that, the predicted ROOH yields—and how they change with temperature—remain uncertain. == Inorganic hydroperoxides ==

Although hydroperoxide often refers to a class of organic compounds, many inorganic or metallo-organic compounds are hydroperoxides. One example involves sodium perborate, a commercially important bleaching agent with the formula . It acts by hydrolysis to give a boron-hydroperoxide: : This hydrogen peroxide then releases hydrogen peroxide: : Several metal hydroperoxide complexes have been characterized by X-ray crystallography, for example: triphenylsilicon and triphenylgermanium hydroperoxides can be obtained by reaction of initial chlorides with excess of hydrogen peroxide in presence of base. Some form by the reaction of metal hydrides with oxygen gas: :{{chem2|L_{n}M\sH + O2 -> L_{n}M\sO\sO\sH}} ({{chem2|L_{n} }} refers to other ligands bound to the metal) Some transition metal dioxygen complexes abstract H atoms (and sometimes protons) to give hydroperoxides: :{{chem2|L_{n}M(O2) + H -> L_{n}MOOH}} ==References==