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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
- ...s in contact with open air. This compounds reacts violently with water and alcohols, releasing a fine mist of sulfuric acid and alkyl sulfates. It has a relati11 KB (1,598 words) - 23:45, 25 August 2020
- ...ice of solvent. Recommended solvents are acetone and isopropanol, as lower alcohols will partially esterify with carboxylic acids, resulting in impurities and7 KB (1,088 words) - 20:32, 28 July 2015
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27 KB (4,285 words) - 21:31, 9 September 2023
- ...ll form an azeotrope. Toluene is miscible with many organic solvents, like alcohols and esters. Toluene has a high refractive index, which causes it to exhibit7 KB (892 words) - 19:16, 15 September 2022
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8 KB (1,049 words) - 23:33, 14 July 2019
- | SolubleOther = Reacts with acids and alkalis<br>Insoluble in alcohols, [[ester]]s, [[ether]]s, halocarbons5 KB (692 words) - 14:01, 23 May 2021
- | SolubleOther = Soluble in [[acetone]], [[ethyl acetate]] and short alcohols<br>Insoluble in [[benzene]], [[chloroform]], [[toluene]], [[diethyl ether]] ...soluble in water, 209 g/100 ml at 25 °C. It is also soluble in low chain alcohols. For other solubilities refer to the info box. It is soluble in iso-butanol8 KB (1,080 words) - 09:06, 14 August 2023
- ...water. It's smell is described as closer to acetone than other short chain alcohols like ethanol. It burns on contact with cuts (like ethanol) and it's widely [[Category:Alcohols]]8 KB (1,041 words) - 10:33, 30 July 2023
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8 KB (1,003 words) - 14:48, 18 November 2023
- [[Category:Alcohols]] [[Category:Primary alcohols]]5 KB (552 words) - 14:42, 19 April 2020
- ...a chromate ester as an intermediate, similar to other esters produced from alcohols. Decomposition of the ester forms a carbonyl group in the new structure, co ...tion is not inherently selective in producing aldehydes alone from primary alcohols. A work-around may be to drip Jones reagent into a large excess of the alco5 KB (879 words) - 18:55, 11 July 2019
- ...grade products including KOH, NaOH, HCl<sub>(aq)</sub>, NH<sub>4</sub>OH, alcohols, glycols. ...d products, inclusing samples of various perfume essences (like ling chain alcohols).21 KB (3,057 words) - 21:32, 19 March 2024
- ...yellow-orange powder that is nearly insoluble in water but soluble in many alcohols. This makes it especially useful for the production of pH testing strips, a5 KB (658 words) - 21:08, 19 July 2018
- [[Category:Alcohols]]5 KB (560 words) - 13:55, 18 November 2023
- ...d [[hydrochloric acid]]s, can be used to oxidize [[primary alcohol|primary alcohols]] to [[aldehyde]]s and [[secondary alcohol]]s to [[ketone]]s.7 KB (974 words) - 17:44, 30 November 2022
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9 KB (1,103 words) - 12:29, 25 June 2023
- ...above 200 °C, in the presence of a tertiary or sterically bulk secondary alcohols, like [[tert-Butanol|t-butanol]] and [[menthol]]. The yield of this route i16 KB (2,327 words) - 18:19, 29 August 2021
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7 KB (831 words) - 17:39, 2 June 2021
- *Ethers and long-chained alcohols must never be distilled to dryness, as they tend form explosive peroxides d ...luminium alloy will react with acids much faster, but will also react with alcohols and even water. Because of this phenomenon, avoid putting gallium on alumin48 KB (5,818 words) - 20:11, 13 March 2024
- ...also soluble in liquid ammonia and pyridine. It is poorly soluble in most alcohols, like [[methanol]] and [[ethanol]].5 KB (609 words) - 18:43, 17 August 2020
- ...at even very low concentrations. It is only very slightly soluble in lower alcohols and other organic solvents, but solubility increases slightly with the addi5 KB (539 words) - 22:20, 11 November 2020
- [[Category:Alcohols]] [[Category:Tertiary alcohols]]5 KB (655 words) - 07:29, 14 February 2021
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5 KB (605 words) - 18:39, 3 October 2018
- Zinc sulfate is a white hygroscopic solid. It is soluble in water and some alcohols. It forms three hydrates.5 KB (650 words) - 20:20, 10 February 2020
- Phenol is weakly acidic, though still more acidic than aliphatic alcohols (about one million times more acidic), and at high pH gives the '''phenoxid10 KB (1,312 words) - 21:33, 5 March 2024
- * Make brominated hydrocarbons from alcohols (useful in making grignards)5 KB (677 words) - 19:21, 20 June 2023
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5 KB (574 words) - 22:53, 22 May 2018
- ...strong fishy-like. It is very soluble in water and organic solvents, like alcohols.8 KB (1,050 words) - 13:47, 26 August 2023
- ...good solubility in water (73.9 g/100 ml at 20 °C), but is less soluble in alcohols and [[ethylene glycol]]. It melts at 66 °C (anhydrous) and 73.9 °C (nonah6 KB (690 words) - 17:03, 26 December 2018
- It is a very potent oxidizer. It oxidizes primary alcohols to carboxylic acids, carboxylic acids to carbon dioxide and water, chlorate11 KB (1,555 words) - 17:28, 30 November 2022
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5 KB (517 words) - 21:17, 9 January 2022
- As it is sensitive to moisture and alcohols, it's best to store it in a hermetically sealed container, a desiccator or6 KB (790 words) - 00:11, 11 December 2019
- | SolubleOther = Slowly reacts with alcohols<br>Insoluble in [[acetone]], [[acetonitrile]], [[dichloromethane]]6 KB (717 words) - 16:43, 30 July 2023
- [[Category:Alcohols]] [[Category:Sugar alcohols]]5 KB (624 words) - 17:51, 3 December 2021
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8 KB (1,057 words) - 08:26, 27 July 2019
- | SolubleOther = Miscible with hydrocarbons, anhydrous alcohols<br>Insoluble in [[glycerol]]5 KB (546 words) - 15:21, 18 November 2023
- [[Category:Alcohols]] [[Category:Sugar alcohols]]4 KB (431 words) - 19:31, 28 June 2017
- ...[sucrose]]). It is soluble in water, but less so in organic solvents, like alcohols and [[acetone]]. ...countries. It is slightly less sweet than sucrose, but unlike other sugar alcohols it does not have a laxative effect at low doses for most people. Consuming5 KB (570 words) - 13:58, 16 April 2023
- [[Category:Alcohols]]5 KB (617 words) - 16:15, 2 January 2022
- | SolubleOther = Reacts with [[amine]]s, alkali<br> Slightly soluble in alcohols ...oiodic acid. The dissolution is exothermic. It is also slightly soluble in alcohols.7 KB (872 words) - 23:09, 28 March 2020
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6 KB (688 words) - 15:30, 24 October 2018
- Symmetric ethers are commonly prepared via acid catalyzed dehydration of alcohols.1 KB (196 words) - 21:59, 1 December 2018
- ...g/L at 20 °C), although it will form emulsions. It is however soluble in alcohols and ether It has a strong odor which is reminiscent of fruity candy and blu5 KB (542 words) - 21:21, 13 September 2020
- Aluminium sulfide will react with alcohols at high temperature to give their respective thiols. such as: With [[methan6 KB (790 words) - 19:18, 19 July 2017
- | SolubleOther = Insoluble in alcohols, halocarbons, hydrocarbons ...orless white hygroscopic solid, slightly soluble in water and insoluble in alcohols.6 KB (746 words) - 15:14, 18 November 2023
- The same reaction also happens with alcohols, giving barium alkoxide.9 KB (1,241 words) - 21:55, 14 May 2018
- ...ss.org/whisper/viewthread.php?tid=15171 Synthesis of longer chain tertiary alcohols]''16 KB (1,869 words) - 16:27, 13 March 2024
- [[Category:Alcohols]]5 KB (656 words) - 08:55, 5 August 2021
- Water is also a polar solvent, as are alcohols.3 KB (509 words) - 15:45, 10 March 2017
- Many chemicals, such as [[ether]]s or secondary alcohols, tend to undergo autoxidation when in contact with air. Halogenated carbons ...c acid]] will serve as nourishment for mold or other biological organisms. Alcohols, like [[ethanol]], will not turn into their respective carboxylic acids (li20 KB (2,386 words) - 20:46, 1 March 2021