Fenton's reagent

One example is the hydroxylation of benzene by Fenton's reagent.

As an example tert-butanol is dimerized with Fenton's reagent and sulfuric acid to 2,5-dimethyl-2,5-hexanediol.

This is used in some organic chemistry oxidations, e.g. in the Fenton's reagent.

This technology is based on Fenton's reaction (Fenton's reagent).

Fenton's reagent was initially used to treat hydrocarbon sites where benzene, toluene, and ethylbenzene were present.

Fenton's reagent is basically a mixture of ferrous iron salts as a catalyst and hydrogen peroxide.

The chemicals used in the process are detrimental to microbes and rapidly degrade the soil, so Fenton's reagent must be used with extreme caution.

Fenton's reagent is a solution of hydrogen peroxide and an iron catalyst that is used to oxidize contaminants or waste waters.

Fenton's reagent in particular is highly exothermic and can cause unwanted effects on microbial life in the aquifer if it is not used carefully.

Examples of organic reagents include the Collins reagent, Fenton's reagent, and Grignard reagent.

Due to this, there are controversies on whether ISCO using Fenton's reagent is really a Fenton reaction.

He was also active in the research of combustion reactions, the separation of gold from sea water, adsorption effects, electrochemistry, and free radical research (see Fenton's reagent).

Fenton's reagent can be used to destroy organic compounds such as trichloroethylene (TCE) and tetrachloroethylene (PCE).

Fenton's reagent (hydrogen peroxide catalyzed with iron) and potassium permanganate are the oxidants that have been used the longest, and are now used the most widely.

He is remembered, however, in the context of Fenton's reagent - hydrogen peroxide containing a trace of ferrous salt, used to convert α-hydroxy acids to α-keto acids.

Oxidation of an organic compound by Fenton's reagent is rapid and exothermic (heat-producing) and results in the oxidation of contaminants to primarily carbon dioxide and water.

Fenton's reagent is also used in organic synthesis for the hydroxylation of arenes in a radical substitution reaction such as the classical conversion of benzene into phenol.

For example, vitamin C has antioxidant activity when it reduces oxidizing substances such as hydrogen peroxide, however, it will also reduce metal ions that generate free radicals through the Fenton's reagent.