Search results
Results from the WOW.Com Content Network
The hydroxyl radical is often referred to as the "detergent" of the troposphere because it reacts with many pollutants, often acting as the first step to their removal. It also has an important role in eliminating some greenhouse gases like methane and ozone. [3] The rate of reaction with the hydroxyl radical often determines how long many ...
In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formula −OH and composed of one oxygen atom covalently bonded to one hydrogen atom. In organic chemistry , alcohols and carboxylic acids contain one or more hydroxy groups.
2-Mercaptoethanol (also β-mercaptoethanol, BME, 2BME, 2-ME or β-met) is the chemical compound with the formula HOCH 2 CH 2 SH. ME or βME, as it is commonly abbreviated, is used to reduce disulfide bonds and can act as a biological antioxidant by scavenging hydroxyl radicals (amongst others). It is widely used because the hydroxyl group ...
The hydroxyl radical, Lewis structure shown, contains one unpaired electron. Lewis dot structure of a Hydroxide ion compared to a hydroxyl radical. In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron.
The fact that oxygen changes the radiation chemistry might be one reason why oxygenated tissues are more sensitive to irradiation than the deoxygenated tissue at the center of a tumor. The free radicals, such as the hydroxyl radical, chemically modify biomolecules such as DNA, leading to damage such as breaks in the DNA strands. Some substances ...
The hydroxyl radical • OH combines with H 2 S to form HS • and water. [21] Other reactions investigated by Tiee (1981) are HS • + ethylene, HS • + O 2 → HO • + SO, and reactions with itself HS • + HS • → H 2 S 2 or H 2 and S. [22] The disulfide can further react with HS • to make the disulfide radical HS–S • and H 2 S. [19]
Ultimately, both reactions generate hydroxyl radicals. These radicals are oxidative in nature and nonselective with a redox potential of E 0 = +3.06 V. [24] This is significantly greater than many common organic compounds, which typically are not greater than E 0 = +2.00 V. [25] This results in the non-selective oxidative behavior of these ...
The free radicals generated by this process engage in secondary reactions. For example, the hydroxyl is a powerful, non-selective oxidant. [6] Oxidation of an organic compound by Fenton's reagent is rapid and exothermic and results in the oxidation of contaminants to primarily carbon dioxide and water.