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  • ...he Brønsted-Lowry definition. Lewis acids belong in the subcategory Lewis acids. This is for simplicity and organizational purposes.
    104 members (8 subcategories, 0 files) - 19:06, 20 April 2019
  • [[Category:Acids]]
    21 members (0 subcategories, 0 files) - 07:15, 17 October 2015
  • Carboxylic acids are weak acids with a -COOH unit. [[Category:Acids]]
    53 members (9 subcategories, 0 files) - 17:14, 16 April 2018
  • 9 members (0 subcategories, 0 files) - 19:04, 20 April 2019
  • Mineral acids are generally those that are inorganic in composition. [[Category:Acids]]
    28 members (0 subcategories, 0 files) - 10:24, 10 July 2016
  • Hydrohalic acids are aqueous solutions of hydrogen halides. [[Category:Acids]]
    4 members (0 subcategories, 0 files) - 10:02, 10 July 2016
  • 7 members (1 subcategory, 0 files) - 14:03, 9 July 2016
  • Acids that do not dissociate completely and have a very low ratio of dissociation [[Category:Acids]]
    32 members (0 subcategories, 0 files) - 07:20, 17 October 2015
  • Acids that do not dissociate completely, but have a high ratio of dissociation. [[Category:Acids]]
    20 members (0 subcategories, 0 files) - 07:16, 17 October 2015
  • [[Category:Carboxylic acids]]
    5 members (0 subcategories, 0 files) - 21:44, 31 October 2016
  • Amino acids are organic compounds containing amine (-NH<sub>2</sub>) and carboxyl (-COO [[Category:Carboxylic acids]]
    3 members (0 subcategories, 0 files) - 19:52, 25 November 2018
  • [[Category:Carboxylic acids]]
    1 member (0 subcategories, 0 files) - 21:00, 17 November 2018
  • Carboxylic acids with an OH group positioned on the next carbon attached to the carboxyl gro [[Category:Carboxylic acids]]
    4 members (1 subcategory, 0 files) - 17:47, 25 November 2018
  • α-Hydroxy acids, or alpha hydroxy acids (AHAs), are a class of chemical compounds that consist of a carboxylic acid [[Category:Carboxylic acids]]
    2 members (0 subcategories, 0 files) - 17:47, 25 November 2018
  • Carboxylic acids that have double or triple covalent bonds between adjacent carbon atoms. [[Category:Carboxylic acids]]
    2 members (0 subcategories, 0 files) - 20:58, 26 November 2018
  • 1 member (0 subcategories, 0 files) - 23:04, 2 January 2020
  • 1 member (0 subcategories, 0 files) - 19:13, 2 February 2020
  • Keto acids or ketoacids (also called oxo acids or oxoacids) are organic compounds that contain a carboxylic acid group and [[Category:Carboxylic acids]]
    2 members (1 subcategory, 0 files) - 18:37, 29 November 2020
  • Alpha-keto acids are carboxylic acids that have the keto group adjacent to the carboxylic acid. [[Category:Carboxylic acids]]
    1 member (0 subcategories, 0 files) - 18:38, 29 November 2020

Page text matches

  • [[Category:Acids]] [[Category:Weak acids]]
    11 KB (1,554 words) - 14:43, 18 November 2023
  • ...es not associate completely, but achieves an equilibrium between conjugate acids and bases. ...ases. Such compounds are said to be weaker bases than water. The conjugate acids of these "bases" - usually exotic oniums like phosphonium or methanium - ar
    4 KB (693 words) - 14:17, 23 November 2016
  • ...ted above 1000 °C. It will dissolve in alkali solutions and non-oxidizing acids, such as [[hydrochloric acid]] releasing hydrogen gas, but not in [[nitric Bulk beryllium metal should be kept away from strong acids or sharp objects. Powdered beryllium must be kept in closed containers, awa
    9 KB (1,264 words) - 13:34, 17 March 2018
  • | SolubleOther = Reacts with acids
    4 KB (482 words) - 10:01, 19 November 2017
  • ...e]] rapidly hydrolyse in moist air and water. Bismuth will react with most acids, but [[oxygen]] or [[hydrogen peroxide]] has to be present to oxidize the m
    11 KB (1,551 words) - 22:07, 19 October 2020
  • | SolubleOther = Dissolves in acids
    5 KB (592 words) - 15:16, 18 November 2023
  • ...g water will quickly break apart the molecule into the two smaller organic acids. The solid must be protected from air as moisture in the air will also degr [[Category:Acids]]
    6 KB (827 words) - 15:31, 20 May 2020
  • [[Category:Mineral acids]] [[Category:Acids]]
    6 KB (692 words) - 13:57, 18 November 2023
  • ...rtin periodinane]]. The direct oxidation of primary alcohols to carboxylic acids can be carried out using [[potassium permanganate]] or the [[Jones reagent] ...ves salt-like compounds called alkoxides. Because most alcohols are weaker acids than water, alkoxides are typically hydrolyzed fully and irreversibly into
    6 KB (832 words) - 21:26, 29 June 2019
  • 10 KB (1,388 words) - 15:49, 25 February 2018
  • ...amounts of phosphorus, it is also capable of α-chlorination of carboxylic acids and is the reagent of choice from the bromination of sensitive alcohols. Bo
    14 KB (1,973 words) - 11:41, 25 June 2023
  • ...in glacial acetic acid as a step in the production of camphor. With dilute acids, terpin hydrate becomes the major product.
    5 KB (663 words) - 23:53, 25 August 2020
  • Aluminium will react with strong acids to form its corresponding salt, except [[nitric acid]], where a [[Passivati ...react violently with water in this form. Aluminum reacts more readily with acids and bases than other metals, as well as solutions of less-reactive metal io
    14 KB (1,991 words) - 11:52, 25 June 2023
  • ...metal being partly protected by insoluble white [[calcium hydroxide]]. In acids where the calcium salt is soluble, the metal reacts vigorously. Calcium metal is hazardous because of it reacts violently with water and acids. Calcium metal is found in some drain cleaners, where it functions to gener
    11 KB (1,502 words) - 15:50, 22 December 2022
  • [[Category:Lewis acids]]
    6 KB (716 words) - 18:37, 7 February 2024
  • ...the trick, preferably cheap ones, such as acetic acid or vinegar. Volatile acids however may generate a thick fog of ammonia salts, which are notorious for
    11 KB (1,471 words) - 22:56, 24 August 2023
  • | SolubleOther = Reacts with alcohols, carboxylic acids, mineral acids<br>Insoluble in all solvents Pure calcium carbide reacts slowly with anhydrous acids.
    9 KB (1,277 words) - 13:58, 18 November 2023
  • | SolubleOther = Reacts with strong acids<br>Soluble in [[acetone]], [[ammonia]], [[ethanol]], [[sulfur dioxide]]
    5 KB (645 words) - 21:52, 5 January 2022
  • | SolubleOther = Reacts with acids<br>Insoluble in organic solvents
    10 KB (1,377 words) - 19:55, 9 September 2023
  • When treated with acids, it releases carbon dioxide:
    6 KB (816 words) - 14:47, 18 November 2023

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