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6 KB (658 words) - 10:28, 27 December 2023
- Acetic acid will react with alcohols in the presence of a catalyst, such as [[sulfuric acid]] to form [[ester]]s11 KB (1,554 words) - 14:43, 18 November 2023
- | SolubleOther = Soluble in alcohols6 KB (827 words) - 15:31, 20 May 2020
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6 KB (692 words) - 13:57, 18 November 2023
- '''Alcohols''' are organic compounds which contain a hydroxyl functional group (-OH) bo == Types of Alcohols ==6 KB (832 words) - 21:26, 29 June 2019
- Many alkyl alcohols will dehydrate to an [[ester]] on addition of [[nitric acid]] with loss of2 KB (205 words) - 17:55, 24 January 2020
- ...xylic acids and is the reagent of choice from the bromination of sensitive alcohols. Both of these reactions occur via a [[phosphorus tribromide]]; alternative14 KB (1,973 words) - 11:41, 25 June 2023
- *Butyl alcohols5 KB (569 words) - 19:01, 25 September 2022
- [[Category:Alcohols]] [[Category:Primary alcohols]]7 KB (908 words) - 21:07, 12 September 2019
- ...lacial acetic acid]], a useful reagent. Calcium acetate will also gel many alcohols if mixed in correct proportions. Too much calcium acetate will revert the g5 KB (677 words) - 15:15, 18 November 2023
- | SolubleOther = Reacts with alcohols, carboxylic acids, mineral acids<br>Insoluble in all solvents ...es, is a superbase. It is capable of deprotonating not just water but also alcohols, evolving acetylene.9 KB (1,277 words) - 13:58, 18 November 2023
- * Make [[calcium acetate]] for gelling alcohols and production of [[acetone]]10 KB (1,377 words) - 19:55, 9 September 2023
- * Remove alcohols from esters (from the reaction product of esterifications)8 KB (1,076 words) - 21:01, 22 March 2021
- ...er = Reacts with acids<br>Slightly soluble in [[glycerol]]<br>Insoluble in alcohols, alkanes8 KB (1,050 words) - 20:51, 6 June 2018
- ...lames after a few seconds. This reaction also works with many other simple alcohols and polyols like [[glycerol]] and some sugars. This is similar to the react6 KB (706 words) - 18:37, 2 June 2021
- ...p://www.sciencemadness.org/talk/viewthread.php?tid=12655 Calcium oxide and alcohols/ethers]8 KB (1,039 words) - 23:42, 20 March 2020
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5 KB (608 words) - 11:11, 2 November 2019
- ...d, soluble in water, with a sour taste. It is soluble in water, less so in alcohols, [[glycerol]], [[propylene glycol]], and insoluble in [[benzene]], [[chloro6 KB (692 words) - 19:51, 16 October 2022
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28 KB (2,574 words) - 17:03, 26 March 2019
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5 KB (543 words) - 22:36, 28 August 2018
- 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
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6 KB (801 words) - 17:05, 8 January 2020
- | SolubleOther = Soluble in alcohols9 KB (1,223 words) - 00:12, 29 March 2020
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5 KB (667 words) - 12:48, 17 June 2019
- ...o carbon dioxide and water. However, chromic acid will (violently) oxidize alcohols to their respective aldehydes or ketones, which cannot be oxidized further | style="text-align:center;"| Lots of water in an open space; low chain alcohols347 KB (46,057 words) - 20:09, 13 March 2024
- ...m will slowly form. Other tertiary alcohols, and even bulk chain secondary alcohols have been shown to work just as good. The reaction mixture can then be dump13 KB (1,879 words) - 20:16, 17 September 2022
- ...es oxidation]] to oxidize primary alcohols to [[aldehyde]]s, and secondary alcohols to [[ketone]]s. The dichromate is reduced to Cr(III) in these reactions, th10 KB (1,262 words) - 21:32, 16 October 2022
- ...rong acids will oxidize primary alcohols to carboxylic acids and secondary alcohols to ketones. *Oxidize alcohols to carboxylic acids and ketones9 KB (1,171 words) - 21:27, 21 September 2023
- [[Category:Alcohols]] [[Category:Primary alcohols]]4 KB (433 words) - 11:13, 9 June 2023
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9 KB (1,194 words) - 18:31, 3 February 2024
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6 KB (704 words) - 20:06, 21 January 2020