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- [[Category:Aryl halides]]4 KB (458 words) - 20:56, 2 December 2018
- | style="text-align:center;"| Alkyl and aryl halides, esters, ethers, halogenated solvents19 KB (2,493 words) - 16:52, 25 July 2023
- *Converted aryl halides to aryl aldehyde ([[Sommelet reaction]]) *Preparation of primary alkyl or aryl amines from aryl or alkyl halides ([[Delépine reaction]])8 KB (1,003 words) - 14:48, 18 November 2023
- *amines of the formula NH<sub>3−x</sub>R<sub>x</sub>, where R = alkyl or aryl. Pyridine and its derivatives are also included here. ...hines of the formula PR<sub>3−x</sub>A<sub>x</sub>, where R = alkyl, A = aryl.1 KB (179 words) - 20:02, 10 April 2023
- '''Ethers''' are a class of organic compounds, where two alkyl or aryl groups are connected to an oxygen atom. The general formula for an ether is1 KB (196 words) - 21:59, 1 December 2018
- ...tone with one methyl group (R–CO–CH<sub>3</sub>, where R = H, alkyl or aryl) in the presence of a base.2 KB (241 words) - 15:52, 30 May 2018
- [[Category:Aryl halides]]6 KB (661 words) - 20:54, 16 May 2021
- ...lic chemistry|organometallic chemical]] reaction in which alkyl, vinyl, or aryl-magnesium halides, known as [[Grignard reagent]]s add to a carbonyl group i1 KB (202 words) - 21:10, 30 November 2018
- '''Grignard reagents''' are alkyl, vinyl, or aryl-[[magnesium]] halides, with the general formula R-MgX, where R is the organ6 KB (857 words) - 14:37, 1 April 2019
- Aryl thiols can also be chlorinated this way. ...s passed through the hot solution until no more gas is absorbed. The crude aryl chloride is purified via separation and distillation.1 KB (214 words) - 18:52, 5 July 2019
- ...[[hydrogen]] atoms have been replaced by a substituent such as an alkyl or aryl group. ...ve the general formula NH<sub>3−x</sub>R<sub>x</sub>, where R = alkyl or aryl and x is the number of substituted groups.2 KB (278 words) - 15:35, 29 August 2017
- *Prepare aromatic aldehydes from aryl halides ([[benzaldehyde]] from [[benzyl chloride]] e.g.)721 B (89 words) - 16:51, 3 November 2018
- ..., and α-carbonyl halides. Secondary halides are far less reactive. Vinyl, aryl and tertiary alkyl halides are unreactive.2 KB (285 words) - 19:55, 18 May 2019
- '''Benzophenone''' is the simplest di-[[aryl]] [[ketone]].4 KB (497 words) - 10:13, 9 July 2022
- |[https://www.youtube.com/channel/UCP5KSO8JNiXSLY9bW24Ko2A Sec. Aryl]57 KB (7,679 words) - 14:44, 18 February 2024
- Another but more specialized method for making aryl-NO<sub>2</sub> group starts from halogenated phenols, is the Zinke nitratio6 KB (839 words) - 21:28, 26 October 2020
- where R is [[alkyl]] or [[aryl]], and where ArOH is BHT or related phenolic antioxidants. Each BHT consume5 KB (560 words) - 17:13, 30 November 2022
- ...O<sub>2</sub> group. Nitrites have the general formula RONO, where R is an aryl or alkyl group. Isopropyl nitrite and other alkyl nitrites are used in medi3 KB (473 words) - 00:51, 29 March 2020
- ...that would require the formation of unstable carbocations (methyl, vinyl, aryl or primary carbon) proceed via S<sub>N</sub>2 mechanism. The hydrohalic aci3 KB (518 words) - 16:20, 6 June 2020
- [[Category:Aryl halides]]5 KB (626 words) - 20:47, 16 May 2021