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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. Brønsted–Lowry acid–base theory - Wikipedia

    en.wikipedia.org/wiki/Brønsted–Lowry_acid...

    Because DMSO accepts protons more strongly than H 2 O the acid becomes stronger in this solvent than in water. [11] Indeed, many molecules behave as acids in non-aqueous solutions but not in aqueous solutions. An extreme case occurs with carbon acids, where a proton is extracted from a C−H bond. [12] Some non-aqueous solvents can behave as acids.

  4. Superacid - Wikipedia

    en.wikipedia.org/wiki/Superacid

    Another group of superacids, the carborane acid group, contains some of the strongest known acids. Finally, when treated with anhydrous acid, zeolites (microporous aluminosilicate minerals) will contain superacidic sites within their pores. These materials are used on massive scale by the petrochemical industry in the upgrading of hydrocarbons ...

  5. Energy level - Wikipedia

    en.wikipedia.org/wiki/Energy_level

    The energy level of the bonding orbitals is lower, and the energy level of the antibonding orbitals is higher. For the bond in the molecule to be stable, the covalent bonding electrons occupy the lower energy bonding orbital, which may be signified by such symbols as σ or π depending on the situation.

  6. HSAB theory - Wikipedia

    en.wikipedia.org/wiki/HSAB_theory

    An alternative quantitative measure is the heat of formation of the Lewis acid-base adduct in a non-coordinating solvent. The ECW model is quantitative model that describes and predicts the strength of Lewis acid base interactions, -ΔH . The model assigned E and C parameters to many Lewis acids and bases.

  7. Hydroxyl radical - Wikipedia

    en.wikipedia.org/wiki/Hydroxyl_radical

    The hydroxyl radical can damage virtually all types of macromolecules: carbohydrates, nucleic acids , lipids (lipid peroxidation) and amino acids (e.g. conversion of Phe to m-Tyrosine and o-Tyrosine). The hydroxyl radical has a very short in vivo half-life of approximately 10 −9 seconds and a high reactivity. [5]

  8. Carbonic acid - Wikipedia

    en.wikipedia.org/wiki/Carbonic_acid

    Carbonic acid is a chemical compound with the chemical formula H 2 C O 3. The molecule rapidly converts to water and carbon dioxide in the presence of water. However, in the absence of water, it is quite stable at room temperature .

  9. Organic acid - Wikipedia

    en.wikipedia.org/wiki/Organic_acid

    An organic acid is an organic compound with acidic properties. The most common organic acids are the carboxylic acids, whose acidity is associated with their carboxyl group –COOH. Sulfonic acids, containing the group –SO 2 OH, are relatively stronger acids. Alcohols, with –OH, can act as acids but they are usually very weak.