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  • ...ts at room temperature, but at high temperatures it can be attacked by hot acids.
    5 KB (534 words) - 20:58, 23 October 2022
  • | SolubleOther = Reacts with acids In closed bottles, away from light and acids.
    4 KB (365 words) - 18:43, 24 January 2022
  • In closed bottles or plastic bags, away from acids. [[Category:Acids]]
    6 KB (755 words) - 16:43, 31 December 2021
  • ...is highly exothermic. In the hydrogenation of [[vegetable oil]]s and fatty acids, for example, the heat released, about 25 kcal per mole (105 kJ/mol), is su
    3 KB (392 words) - 15:32, 2 January 2022
  • | SolubleOther = Reacts with acids<br>Soluble in [[acetone]], [[benzene]], [[carbon disulfide]], [[carbon tetr ...weak base, with a ''K''<sub>b</sub> of 10<sup>−14</sup>. It reacts with acids to form salts.
    8 KB (943 words) - 22:46, 24 August 2023
  • *Lemon, apple, orange or onion juice (organic acids and the paper forms esters under heat) *Soap solution (carboxylic acids partially oxidize)
    5 KB (707 words) - 21:23, 5 November 2022
  • ...) is a purple-black or brown-black [[ink]] made from iron salts and tannic acids extracted from plant sources. It was the standard ink formulation used in E
    2 KB (336 words) - 21:29, 15 April 2022
  • ...hemically inert. While it is waterproof and resistant to breakdown by dil. acids and bases, it readily dissolves quickly in many non-polar solvents, like ke
    5 KB (611 words) - 11:56, 9 September 2023
  • [[Category:Acids]] [[Category:Weak acids]]
    3 KB (333 words) - 22:10, 29 August 2022
  • [[Category:Carboxylic acids]]
    3 KB (317 words) - 19:20, 23 November 2023
  • [[Category:Carboxylic acids]]
    4 KB (431 words) - 19:26, 23 November 2023
  • | SolubleOther = Reacts with acids<br>Miscible with [[acetone]], alcohols, [[benzene]], [[diethyl ether]], [[T
    4 KB (402 words) - 22:43, 1 September 2022
  • Diborane readily reduces carboxylic acids to the corresponding alcohols, whereas ketones react only sluggishly.
    6 KB (837 words) - 21:16, 2 September 2022
  • 5 KB (597 words) - 21:11, 22 October 2022
  • ...queous phase) are diatomic, inorganic compounds that function as Arrhenius acids. The formula is '''HX''' where X is one of the halogens ([[fluorine]], [[ch .... With the exception of hydrofluoric acid, the hydrogen halides are strong acids, with acid strength increasing down the group. Hydrofluoric acid is complic
    4 KB (526 words) - 19:22, 30 November 2022
  • ...sup>+</sup>) to the surrounding water molecules (H<sub>2</sub>O). In fact, acids must be surrounded by more than a single water molecule in order to ionize, ...acid with an ionization constant of 10<sup>9</sup> or higher may do this. Acids whose ionization constants are below 10<sup>9</sup> generally cannot form s
    2 KB (300 words) - 18:18, 2 January 2023
  • ...zing agents. Organic peroxides tend to be explosive, but some, like peroxy acids are simply powerful oxidizing agents.
    4 KB (526 words) - 12:51, 25 August 2023
  • [[Category:Acids]] [[Category:Weak acids]]
    5 KB (538 words) - 20:39, 14 April 2023
  • | SolubleOther = Reacts with acids<br>Insoluble in organic solvents
    5 KB (628 words) - 21:02, 2 June 2023
  • | SolubleOther = Reacts with acids<br>Insoluble in solvents Like other metal acetylides, it reacts with acids to release [[acetylene]] gas.
    5 KB (653 words) - 21:03, 2 June 2023

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