Search results
Create the page "Nitriles" on this wiki! See also the search results found.
- Aqueous palladium(II) chloride can convert primary amides into nitriles, in a water-acetonitrile 1:1 mixture, the conversion takes place at room te ...le nitriles, with a LD<sub>50</sub> of 2,460 mg/kg, while the next primary nitriles (propionitrile, butyronitrile, malononitrile, acrylonitrile) have LD50 valu8 KB (1,051 words) - 22:14, 15 November 2020
- *Convert primary amides into nitriles6 KB (692 words) - 20:00, 12 September 2021
- *Make nitriles from amides6 KB (750 words) - 09:43, 15 August 2022
- *Make organic nitriles6 KB (794 words) - 13:27, 10 July 2022
- Sodium cyanide reacts with halocarbons to give nitriles. [[Iodine]] can be used as catalyst. *Make nitriles10 KB (1,481 words) - 13:28, 10 July 2022
- [[Category:Nitriles]]6 KB (669 words) - 12:05, 29 December 2020
- ...is routes are hydration of alkynes, reaction of [[Grignard reagent]]s with nitriles, followed by hydrolysis, decarboxylation of carboxylic anhydrides, oxidatio3 KB (428 words) - 22:37, 10 June 2018
- *Make nitriles2 KB (285 words) - 19:55, 18 May 2019
- *Decarboxylation of α-nitro carboxylic acids formed from nitriles and ethyl nitrate.6 KB (839 words) - 21:28, 26 October 2020
- [[Category:Nitriles]]4 KB (460 words) - 20:50, 2 February 2020
- [[Category:Nitriles]]4 KB (492 words) - 19:50, 29 July 2021
- [[Category:Nitriles]]5 KB (509 words) - 12:12, 29 December 2020
- ...ng than borohydride. As such, it does not reduce amides, ethers, lactones, nitriles, nitro compounds and epoxides.6 KB (625 words) - 21:17, 30 August 2022
- [[Category:Nitriles]]11 KB (1,497 words) - 18:41, 28 March 2024
- Sodium hydrazide reacts with nitriles, followed by water, at low temperatures to yield amidrazones.<ref>Th. Kauff8 KB (1,004 words) - 14:42, 16 August 2023
- [[Category:Nitriles]]7 KB (885 words) - 13:11, 18 November 2023
- [[Category:Nitriles]]6 KB (791 words) - 12:10, 27 December 2023
- ...s''' is a substitution reaction commonly used for the preparation of alkyl nitriles by reaction of the corresponding alkyl halide with a metal cyanide. ...ondary bromides and chlorides react in moderate yields to give the desired nitriles. Tertiary halides mainly undergo side reactions, one of which is the E2 eli3 KB (522 words) - 18:44, 11 March 2024
- ...c synthesis as a strong base, for example for the hydrolysis of esters and nitriles, and as a base in aldol condensations. It can be used to perform decarboxyl8 KB (1,023 words) - 20:49, 13 March 2024