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  • ...de]], [[carbon tetrachloride]], [[chloroform]], [[dichloromethane]], liq [[Hydrogen chloride|HCl]]<br>Readily soluble in [[Titanium(IV) chloride|TiCl<sub>4</su
    8 KB (1,001 words) - 21:15, 22 October 2022
  • ...b>]], [[Tin(IV) chloride|SnCl<sub>4</sub>]]<br>Sparingly soluble in liq. [[hydrogen iodide|HI]] Phosphorus oxychloride reacts with water to form phosphoric acid and hydrogen chloride fumes.
    6 KB (750 words) - 09:43, 15 August 2022
  • ...loride, [[bromoacetic acid]], [[carbon disulfide]], [[chloroform]], liq. [[hydrogen sulfide|H<sub>2</sub>S]], liq. [[sulfur dioxide|SO<sub>2</sub>]] ...at, a solvent can also be used, such as [[carbon tetrachloride]], [[carbon disulfide]] or [[benzene]]. This route is recommended if you're substituting red P wi
    6 KB (765 words) - 20:59, 2 December 2018
  • ...fur dioxide|SO<sub>2</sub>]]<br>sparingly soluble in [[benzene]], [[carbon disulfide]], [[carbon tetrachloride]]
    5 KB (599 words) - 20:58, 2 December 2018
  • ...rbon disulfide]], [[diethyl ether]], liq. [[Hydrogen bromide|HBr]], liq. [[Hydrogen chloride|HCl]], conc. [[sulfuric acid]], [[Tetrahydrofuran|THF]] ...It is soluble in [[diethyl ether]], [[benzene]], [[chloroform]], [[carbon disulfide]], concentrated [[sulfuric acid]].
    5 KB (508 words) - 15:12, 31 December 2018
  • | SolubleOther = Soluble in [[1,4-Dioxane|1,4-dioxane]], [[carbon disulfide|CS<sub>2</sub>]], [[carbon tetrachloride|CCl<sub>4</sub>]], [[chloroform]], ...[[antimony(III) oxide]] with conc. [[hydrochloric acid]], with a bit of [[hydrogen peroxide]] to speed up the reaction. The aq. acid is removed via distillati
    6 KB (803 words) - 12:58, 18 December 2022
  • | cyano || ~C≡N || ~CN || [[cyanogen]] || [[hydrogen cyanide]]<br>prussic acid|| [[cyanide]] || cyanido-<br>cyano- || -nitrile<b | isocyano || ~NC || ~N≡C || isocyano-formonitrile || Hydrogen isocyanide<br>isohydrocyanic acid || isocyanide || isocyanido-<br>isocyano-
    4 KB (399 words) - 20:19, 6 September 2022
  • | Formula = '''[[Carbon|C]]'''<sub>13</sub>'''[[Hydrogen|H]]'''<sub>10</sub>'''[[Oxygen|O]]''' ...r = Soluble in glacial [[acetic acid]], [[acetone]], [[benzene]], [[carbon disulfide]], [[carbon tetrachloride|CCl<sub>4</sub>]], [[methanol]]
    4 KB (497 words) - 10:13, 9 July 2022
  • ..., [[methanol]], [[propylene glycol]]<br>Insoluble in [[benzene]], [[carbon disulfide]], [[chloroform]], [[petroleum ether]] ...acetic acid. This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group.
    5 KB (588 words) - 21:39, 13 June 2020
  • | Solvent3 = carbon disulfide TNA will react with [[hydrogen peroxide]] and conc. [[sulfuric acid]] to yield 1,2,4,6-tetranitrobenzene.
    8 KB (913 words) - 19:47, 11 October 2020
  • ...]], [[dioxane]], [[methanol]]<br>Slightly soluble in [[benzene]], [[carbon disulfide]], [[diethyl ether]], [[ethanol]], [[hexane]] Succinonitrile is mainly produced by the addition of [[hydrogen cyanide]] to acrylonitrile:<ref>http://www.mrw.interscience.wiley.com/emrw/
    5 KB (509 words) - 12:12, 29 December 2020
  • ...er = Soluble in [[nitric acid]]<br>Insoluble in [[acetonitrile]], [[carbon disulfide]], [[chloroform]], [[diethyl ether]], [[ethanol]] Iodine pentoxide will react with [[hydrogen sulfide]], forming [[sulfur dioxide]]:
    6 KB (782 words) - 22:30, 5 February 2021
  • vol. 38; (1984); p. 825 - 827</ref> or [[hydrogen peroxide]]<ref>Bray, W. C.; Caulkins, A. L.; Journal of the American Chemic
    8 KB (1,012 words) - 21:27, 24 May 2021
  • ...Reacts with alcohols, amines, bases<br>Miscible with [[benzene]], [[carbon disulfide]], ethers, halocarbons Treating benzoyl chloride with [[hydrogen peroxide]] and sodium hydroxide yields [[benzoyl peroxide]].<ref>https://ww
    6 KB (662 words) - 10:16, 7 July 2022
  • Some proteins can be denatured by 2-mercaptoethanol, which cleaves the disulfide bonds that may form between thiol groups of cysteine residues. 2-Mercaptoethanol is produced from the reaction of [[ethylene oxide]] with [[hydrogen sulfide]]. Thiodiglycol and various zeolites are used to catalyze the react
    4 KB (462 words) - 20:47, 14 November 2021
  • ...Other = Reacts with acids<br>Soluble in [[acetone]], [[benzene]], [[carbon disulfide]], [[carbon tetrachloride]], [[diethyl ether]], [[ethanol]], [[ethyl acetat | Solvent3 = carbon disulfide
    8 KB (943 words) - 22:46, 24 August 2023
  • ...uryl chloride]], [[trifluoroacetic acid]]<br>Sparingly soluble in [[carbon disulfide]], [[carbon tetrachloride|CCl<sub>4</sub>]]<br>Insoluble in hydrocarbons ...sulfuric acid reacts violently with water to yield [[sulfuric acid]] and [[hydrogen chloride]], commonly seen as vapors fuming copiously from the liquid:
    8 KB (1,050 words) - 20:53, 5 November 2023
  • | SolubleOther = Slightly soluble in [[acetone]], [[benzene]], [[carbon disulfide]], [[chloroform]], [[diethyl ether]], [[ethanol]], [[toluene]], [[xylene]] ...011). "Coordination Complexes as Catalysts: The Oxidation of Anthracene by Hydrogen Peroxide in the Presence of VO(acac)2". Journal of Chemical Education. 88 (
    6 KB (673 words) - 20:19, 27 December 2023

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