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  • ...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 relati
    11 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 and
    7 KB (1,088 words) - 20:32, 28 July 2015
  • 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 exhibit
    7 KB (892 words) - 19:16, 15 September 2022
  • 8 KB (1,049 words) - 23:33, 14 July 2019
  • | SolubleOther = Reacts with acids and alkalis<br>Insoluble in alcohols, [[ester]]s, [[ether]]s, halocarbons
    5 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-butanol
    8 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
  • 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 alco
    5 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, a
    5 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
  • 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 i
    16 KB (2,327 words) - 18:19, 29 August 2021
  • 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 alumin
    48 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

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