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  • | OtherNames = Essence of vinegar (concentrated)<br>Hydrogen acetate<br>Methanecarboxylic acid<br>Vinegar (dilute) ...l]], [[hexane]], [[isopropanol]], [[methanol]]<br>Immiscible with [[carbon disulfide]], [[carbon tetrachloride]], [[pentane]]
    11 KB (1,554 words) - 14:43, 18 November 2023
  • ...methylformamide]]<br>Slightly soluble in glacial [[acetic acid]], [[carbon disulfide]], [[ethanol]] ...de, so it will produce a variety of other gases such as[[Hydrogen sulfide| hydrogen sulfide]] and [[phosphine]].
    7 KB (929 words) - 22:12, 29 May 2023
  • | Name = Carbon disulfide | ImageFile = Carbon disulfide syringe sample and original bottle by Thoisoi2.png
    10 KB (1,388 words) - 21:40, 16 October 2022
  • ...is difficult. The best way is to wash the glass with a diluted solution of hydrogen peroxide or a salt such as sodium thiosulfate or metabisulfite. If you're u ...of other solvents, such as acetone, ethyl acetate, THF, chloroform, carbon disulfide, is not recommended, as, apart from wasting large amounts of valuable solve
    11 KB (1,909 words) - 21:41, 2 December 2018
  • ...], [[propylene glycol]]<br>Insoluble in [[acetone]], [[benzene]], [[carbon disulfide]], [[carbon tetrachloride|CCl<sub>4</sub>]], [[chloroform]], [[diethyl ethe ...ed as a solvent. It is a polyol, consisting of a propane molecule with one hydrogen on each of the carbons being substituted by a [[hydroxyl]] group.
    6 KB (707 words) - 14:50, 18 November 2023
  • ...ining plants, must be neutralized with [[Sodium hypochlorite|bleach]] or [[hydrogen peroxide]], to turn them into less harmful cyanates. The resulting cyanates ...ous and carcinogenic. These should be converted to the +3 oxidation state; hydrogen peroxide as well as sulfites or thiosulfate will do this, which is typicall
    347 KB (46,057 words) - 20:09, 13 March 2024
  • ...is insoluble in most common solvents and water, but is soluble in [[carbon disulfide]], [[benzene]], [[toluene]] and [[xylene]]. There are over 30 [[allotrope]] ...dustry to remove hydrogen sulfide. This is a very useful way to neutralize hydrogen sulfide, as opposed to burning it, as it produces elemental sulfur and wate
    12 KB (1,653 words) - 18:25, 13 February 2021
  • ...rug precursors such as gamma-butyrolactone, explosive precursors including hydrogen peroxide, and in some cases even diethyl ether or copper sulfate. ...rbon disulfide]], [[chloroform]], [[formaldehyde]], [[hydrazine]], conc. [[hydrogen peroxide]] (>50%), [[phenol]], [[sulfuric acid]], cyanides, mercury and cad
    15 KB (2,253 words) - 08:21, 25 June 2023
  • | SolubleOther = Soluble in [[acetone]], [[benzene]], [[carbon disulfide|CS<sub>2</sub>]], [[carbon tetrachloride|CCl<sub>4</sub>]], [[chloroform]], ...loride fumes in humid air forming a white smoke of [[tin(IV) oxide]] and [[hydrogen chloride]].
    7 KB (954 words) - 18:13, 7 June 2023
  • ...onoxide<br>Dihydrogen oxide<br>Hydrogen oxide<br>Oxidane<br>Hydric acid<br>Hydrogen hydroxide<br>Hydrogenyl alcohol ...ketone]], [[methyl formate]], [[nitromethane]]<br>Immiscible with [[carbon disulfide]], [[ester]]s, [[ether]]s, halocarbons, hydrocarbons
    8 KB (1,049 words) - 23:33, 14 July 2019
  • | Solvent3 = carbon disulfide Reactions with [[hydrogen peroxide]] form a very unstable organic peroxide explosive, similar to [[ac
    8 KB (1,003 words) - 14:48, 18 November 2023
  • | Chloric acid, chromic acid, chromium (VI) oxide, hydrogen peroxide, manganese (VII) oxide, nitric acid, ozone, perchloric acid, perox | Chloric acid, chromic acid, chromium (VI) oxide, hydrogen peroxide, manganese (VII) oxide, nitric acid, ozone, perchloric acid, perox
    48 KB (5,818 words) - 20:11, 13 March 2024
  • | style="text-align:center;"| Hydrogen | style="text-align:center;"| Hydrogen sulfide (gas)
    174 KB (19,350 words) - 20:07, 13 March 2024
  • ...''' is a gray chemical compound, that readily hydrolyzes in air to release hydrogen sulfide gas. It has the chemical formula '''Al<sub>2</sub>S<sub>3</sub>'''. Aluminium sulfide reacts with water to release [[hydrogen sulfide]]:
    6 KB (790 words) - 19:18, 19 July 2017
  • | OtherNames = Phosphamine<br>Phosphorus trihydride<br>Phosphorated hydrogen | SolubleOther = soluble in alcohol, [[carbon disulfide]], [[diethyl ether]]<br>slightly soluble in [[benzene]], [[chloroform]], [[
    7 KB (904 words) - 15:22, 10 July 2019
  • | SolubleOther = Reacts with alcohols<br>Soluble in [[benzene]], [[carbon disulfide]], [[hexane]], [[1,2-Dichloroethane|1,2-dichloroethane]]<br>Poorly soluble ...decomposes when heated to 200 °C. It is soluble in [[benzene]], [[carbon disulfide]] and fairly soluble in [[hexane]]. Its density is 4.18 g/cm<sup>3</sup> at
    7 KB (863 words) - 19:36, 20 June 2023
  • ...lcohol and its esters, valeric ether<br>Insoluble in [[benzene]], [[carbon disulfide]], [[toluene]] .../sub>''') is an unstable compound formed by the addition of an acidified [[hydrogen peroxide]] solution to solutions of metal chromates, such as sodium or [[po
    6 KB (782 words) - 19:42, 12 February 2023
  • Ammonium azide will detonate to release [[nitrogen]] and [[hydrogen]] gases. ...luble in [[acetone]], [[aniline]], [[benzaldehyde]], [[benzene]], [[carbon disulfide]], [[chlorobenzene]], [[chloroform]], [[diethyl ether]], [[ethyl acetate]],
    6 KB (740 words) - 18:42, 14 October 2019
  • | SolubleOther = Soluble in glacial [[acetic acid]], [[benzene]], [[carbon disulfide]], [[chloroform]], [[diethyl ether]]<br>Slightly soluble in [[glycerol]], o Iodoform can be reduced with [[hydrogen iodide]] to diiodomethane:
    6 KB (734 words) - 16:57, 13 April 2019
  • ...panol]], <br>Insoluble in [[acetone]], [[benzene]], [[petroleum ether]], [[hydrogen sulfide]] Electrolysis of [[sodium nitrate]] in the presence of [[hydrogen chloride]] will also give hydroxylamine. A lead cathode and a coal anode ar
    8 KB (1,041 words) - 16:34, 30 December 2023
  • ...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