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  • 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 valu
    8 KB (1,051 words) - 22:14, 15 November 2020
  • *Convert primary amides into nitriles
    6 KB (692 words) - 20:00, 12 September 2021
  • *Make nitriles from amides
    6 KB (750 words) - 09:43, 15 August 2022
  • *Make organic nitriles
    6 KB (794 words) - 13:27, 10 July 2022
  • Sodium cyanide reacts with halocarbons to give nitriles. [[Iodine]] can be used as catalyst. *Make nitriles
    10 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, oxidatio
    3 KB (428 words) - 22:37, 10 June 2018
  • *Make nitriles
    2 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. Kauff
    8 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 eli
    3 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 decarboxyl
    8 KB (1,023 words) - 20:49, 13 March 2024