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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]]s
    11 KB (1,554 words) - 14:43, 18 November 2023
  • | SolubleOther = Soluble in alcohols
    6 KB (827 words) - 15:31, 20 May 2020
  • 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 of
    2 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]]; alternative
    14 KB (1,973 words) - 11:41, 25 June 2023
  • *Butyl alcohols
    5 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 g
    5 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, alkanes
    8 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 react
    6 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
  • 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]], [[chloro
    6 KB (692 words) - 19:51, 16 October 2022
  • 28 KB (2,574 words) - 17:03, 26 March 2019
  • 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 potass
    6 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
  • 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. It
    19 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
  • 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]]. Bein
    8 KB (996 words) - 15:05, 18 November 2023
  • 6 KB (664 words) - 19:16, 25 November 2021
  • [[Category:Alcohols]] [[Category:Sugar alcohols]]
    6 KB (707 words) - 14:50, 18 November 2023
  • 8 KB (1,127 words) - 00:10, 11 December 2019
  • 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 alcohols
    6 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 ac
    11 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.43
    11 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
  • 6 KB (801 words) - 17:05, 8 January 2020
  • | SolubleOther = Soluble in alcohols
    9 KB (1,223 words) - 00:12, 29 March 2020
  • 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 alcohols
    347 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 dump
    13 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, th
    10 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 ketones
    9 KB (1,171 words) - 21:27, 21 September 2023
  • [[Category:Alcohols]] [[Category:Primary alcohols]]
    4 KB (433 words) - 11:13, 9 June 2023
  • 9 KB (1,194 words) - 18:31, 3 February 2024
  • 6 KB (704 words) - 20:06, 21 January 2020

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