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  2. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    Acid strength is the tendency of an acid, symbolised by the chemical formula, to dissociate into a proton, +, and an anion, .The dissociation or ionization of a strong acid in solution is effectively complete, except in its most concentrated solutions.

  3. Chlorine - Wikipedia

    en.wikipedia.org/wiki/Chlorine

    The primary decay mode of isotopes lighter than 35 Cl is electron capture to isotopes of sulfur; that of isotopes heavier than 37 Cl is beta decay to isotopes of argon; and 36 Cl may decay by either mode to stable 36 S or 36 Ar. [42] 36 Cl occurs in trace quantities in nature as a cosmogenic nuclide in a ratio of about (7–10) × 10 −13 to 1 ...

  4. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    Organochlorine chemistry is concerned with the properties of organochlorine compounds, or organochlorides, organic compounds that contain one or more carbon–chlorine bonds. [1] The chloroalkane class (alkanes with one or more hydrogens substituted by chlorine) includes common examples. The wide structural variety and divergent chemical ...

  5. Oxidizing agent - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_agent

    The international pictogram for oxidizing chemicals. Dangerous goods label for oxidizing agents. An oxidizing agent (also known as an oxidant, oxidizer, electron recipient, or electron acceptor) is a substance in a redox chemical reaction that gains or "accepts"/"receives" an electron from a reducing agent (called the reductant, reducer, or electron donor).

  6. Oxyacid - Wikipedia

    en.wikipedia.org/wiki/Oxyacid

    If there are more than two oxyacids having the same element as the central atom, then, in some cases, acids are distinguished by adding the prefix per-or hypo-to their names. The prefix per-, however, is used only when the central atom is a halogen or a group 7 element. [8] For example, chlorine has the four following oxyacids: hypochlorous ...

  7. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    Phenols are more acidic than typical alcohols. The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pK a is usually between 10 and 12).

  8. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  9. Chlorine-releasing compounds - Wikipedia

    en.wikipedia.org/wiki/Chlorine-releasing_compounds

    The strength of chlorine-releasing solutions, as well as their dosage in uses like water chlorination and pool sanitization, is usually expressed as mass concentration of "free chlorine" or "available chlorine". It is the mass of chlorine gas (Cl 2) that would yield the same oxidizing power as the product contained in (or applied to) a specific ...