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• Benzyl alcohol
  ...g stores as solvent, mostly pure, though most of the time mixed with other solvents. [[Category:Solvents]]
  5 KB (621 words) - 10:50, 9 September 2023
• Nitroethane
  ...id, with a fruity odor, slightly soluble in water, but miscible in organic solvents. ...diethyl ether, [[dimethyl sulfoxide]] or [[dimethylformamide]] are used as solvents instead.<ref>Shao, Yi-Ming; Yang, Wen-Bin; Kuo, Tun-Hsun; Tsai, Keng-Chang;
  7 KB (850 words) - 22:48, 20 January 2020
• Karl Fischer titration
  ...]], or [[methyl cellosolve]] (ethylene glycol monomethyl ether). Alcoholic solvents like these give 1 : 1 reaction stoichiometry. === Additives / co-solvents ===
  10 KB (1,556 words) - 18:24, 17 April 2019
• Dimethylzinc
  ...t reacts with all protic solvents, but is very soluble in many hydrocarbon solvents, like alkanes and aromatics.
  7 KB (843 words) - 22:43, 17 November 2020
• Benzoyl chloride
  ...iquid, with a pungent aromatic odor. It reacts with water and other protic solvents.
  6 KB (662 words) - 10:16, 7 July 2022
• Solvent
  Solvents can be broadly classified into two categories: polar and non-polar. A speci ...ty of water is indicated by its high dielectric constant of 88 (at 0 °C). Solvents with a dielectric constant of less than 15 are generally considered to be n
  2 KB (288 words) - 19:42, 11 October 2022
• Chlorosulfuric acid
  ...c and a powerful lachrymator. It reacts with water and alcohols and protic solvents, but dissolves in halocarbons.
  8 KB (1,050 words) - 20:53, 5 November 2023
• Kolbe nitrile synthesis
  ...th the application of alkali cyanides such as [[sodium cyanide]] and polar solvents the reaction type is an S_N2 reaction whereby the alkyl halide is ...ciples, the carbon center is more basic and more nucleophilic. When protic solvents are used, the resulting greater solvation of this carbon center is thought
  3 KB (522 words) - 18:44, 11 March 2024