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- Chromium(III) sulfate is readily soluble in water and some lower alcohols. ...hromate]] or [[sodium dichromate]] acidified with sulfuric acid to oxidize alcohols, produces chromium(III) sulfate as a byproduct, along with sodium or potass6 KB (795 words) - 16:52, 6 November 2018
- ...dorless white crystalline solid, soluble in water, but almost insoluble in alcohols.5 KB (605 words) - 22:41, 17 October 2020
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7 KB (964 words) - 18:49, 28 March 2021
- ...ith a pungent irritating odor, that fumes in air. It reacts with water and alcohols.5 KB (588 words) - 20:42, 22 November 2020
- ...tion. Substances commonly used for this purpose include [[magnesium]] (for alcohols), [[calcium oxide]], [[calcium hydride]], [[phosphorus pentoxide]], and [[s ...20 to 50ppm). This technique is not compatible with protic solvents (like alcohols) or halogenated solvents, as these will react directly with the sodium. It19 KB (2,493 words) - 16:52, 25 July 2023
- ...ester from an [[alcohol]] and a [[carboxylic acid]]. Carboxylic acids and alcohols esterify in small amounts according to a reversible equation:2 KB (340 words) - 15:26, 6 April 2022
- ...carbonate]]. [[Calcium oxide]] can also be used. Ethanol, like most other alcohols, is highly flammable, even in low concentrations in solution, although at l [[Category:Alcohols]]14 KB (1,953 words) - 20:56, 9 September 2023
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6 KB (820 words) - 18:00, 5 August 2019
- [[Category:Alcohols]]5 KB (501 words) - 13:36, 20 November 2020
- ...ic acids, formic acid is easily [[esterification|esterified]] with primary alcohols, often forming pleasant-smelling compounds such as [[methyl formate]]. Bein8 KB (996 words) - 15:05, 18 November 2023
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6 KB (664 words) - 19:16, 25 November 2021
- [[Category:Alcohols]] [[Category:Sugar alcohols]]6 KB (707 words) - 14:50, 18 November 2023
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8 KB (1,127 words) - 00:10, 11 December 2019
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5 KB (592 words) - 17:58, 8 November 2023
- ...commonly used for the reduction of esters and carboxylic acids to primary alcohols. *Reducing esters to alcohols6 KB (799 words) - 17:39, 29 February 2020
- ...s is rarer, as methanol is cheaper than the other alcohols. Some technical alcohols are nothing but almost pure MeOH mixed with dye. Methanol is significantly more toxic than other common alcohols such as [[ethanol]] or [[isopropanol]], as it is metabolized to [[formic ac11 KB (1,601 words) - 18:39, 9 July 2023
- ...c Chemistry including Medicinal Chemistry, Mild and selective oxidation of alcohols and deoximation of oximes over supported quinolinium fluorochromate, Vol.4311 KB (1,468 words) - 18:42, 27 May 2023
- ...s reactions, naphthalene can also be alkylated by reaction with alkenes or alcohols, with sulfuric or phosphoric acid as the catalyst.7 KB (924 words) - 15:02, 18 November 2023
- | SolubleOther = Reacts with alcohols<br>Soluble in [[carbon tetrachloride]], [[chloroform]], [[nitric acid]]6 KB (825 words) - 18:56, 12 October 2018
- ...poorly soluble in water, but miscible with other organic solvents, such as alcohols. It freezes at −29 °C and boils at around 100 °C.10 KB (1,375 words) - 20:01, 16 May 2023