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• Sodium oxide
  ...er = Reacts with alcohols, [[carboxylic acid]]s, esters, halogens, mineral acids<br>Insoluble in [[ether]]s, hydrocarbons ...he decomposition begins at 218 °C, yielding sodium oxide and furanes.<ref>Lewis, R.J. Sr. (ed) Sax's Dangerous Properties of Industrial Materials. 11th Edi
  5 KB (655 words) - 19:10, 6 February 2020
• Titanium(IV) chloride
  [[Category:Lewis acids]]
  5 KB (622 words) - 21:01, 5 June 2021
• Chromium(III) chloride
  [[Category:Lewis acids]]
  5 KB (542 words) - 21:34, 7 May 2020
• Blanc reaction
  ...hyde]] and [[hydrogen chloride]] catalyzed by [[zinc chloride]] or other [[Lewis acid]]s to form chloromethyl arenes.
  1 KB (214 words) - 18:52, 5 July 2019
• Amine
  Amines react with acids to form alkyl- or aryl-ammonium salts. [[Category:Lewis bases]]
  2 KB (278 words) - 15:35, 29 August 2017
• Friedel-Crafts reaction
  ...ves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid, such as [[aluminium chloride]], [[iron(III) chloride]], or other MXn ...wever, because the product ketone forms a rather stable complex with Lewis acids such as AlCl3, a stoichiometric amount or more of the "catalyst" must gener
  2 KB (230 words) - 21:46, 11 October 2022
• Triphenylphosphine
  Triphenylphosphine is a weak base, but does form stable salts with strong acids such as HCl and HBr. [[Category:Lewis bases]]
  4 KB (456 words) - 14:18, 6 October 2019
• Trimethylphosphine
  Trimethylphosphine is a weak [[base]], but does form stable salts with strong acids. [[Category:Lewis bases]]
  5 KB (594 words) - 22:30, 21 January 2020
• Ether cleavage
  ...[[ether]]s. The most common reagents used in ether cleavage are hydrohalic acids and certain organolithium compounds. ...[hydrofluoric acid]] to cleave ethers in protic media. Usage of hydrohalic acids takes advantage of the fact that these agents are able to protonate the eth
  3 KB (518 words) - 16:20, 6 June 2020
• Benzylamine
  Benzylamine reacts with acids forming salts. [[Category:Lewis bases]]
  5 KB (561 words) - 11:40, 20 August 2020
• Ethylamine
  | SolubleOther = Reacts with acids<br>Miscible with [[acetone]], [[benzene]], [[diethyl ether]], [[ethanol]], Ethylamine reacts with acids to form their respective salts.
  7 KB (882 words) - 21:56, 15 November 2020
• Purple acid
  *Similarly adducts of NO with strong Lewis acids are known, such as with HCl, BF₃ and SO₃. [[Category:Acids]]
  9 KB (1,331 words) - 13:07, 28 January 2023
• Aluminium iodide
  Anhydrous AlI₃ is a strong Lewis acid and will absorb water from the atmosphere to form hexahydrate. [[Category:Lewis acids]]
  6 KB (800 words) - 13:19, 18 November 2023
• Diphenylamine
  | SolubleOther = Reacts with acids<br>Soluble in [[acetone]], [[benzene]], [[carbon disulfide]], [[carbon tetr ...weak base, with a ''K''_b of 10⁻¹⁴. It reacts with acids to form salts.
  8 KB (943 words) - 22:46, 24 August 2023
• Boron trichloride
  As a strong Lewis acid, BCl₃ forms adducts with tertiary amines, phosphines, ether
  5 KB (597 words) - 21:11, 22 October 2022
• Trimethylamine
  | SolubleOther = Reacts with acids<br>Miscible with [[alcohol]]s, aromatics, [[ester]]s, [[ether]]s, halocarbo Trimethylamine reacts with acids forming trimethylammonium salts.
  6 KB (706 words) - 22:03, 25 December 2023