Search results

Jump to: navigation, search
  • Aqueous palladium(II) chloride can convert primary amides into nitriles, in a water-acetonitrile 1:1 mixture, the conversion takes pl
    8 KB (1,051 words) - 22:14, 15 November 2020
  • 7 KB (929 words) - 22:12, 29 May 2023
  • [[Ammonia]] will be deprotonated in the presence of strong bases to form amides.
    2 KB (283 words) - 12:34, 25 June 2023
  • *Reduce amides to amines
    6 KB (799 words) - 17:39, 29 February 2020
  • 8 KB (1,070 words) - 13:27, 10 July 2022
  • *Convert primary amides into nitriles
    6 KB (692 words) - 20:00, 12 September 2021
  • ...ylamine is a base commonly used in organic chemistry to prepare esters and amides from acyl chlorides. Like other tertiary amines,it catalyzes the formation
    5 KB (586 words) - 14:59, 25 December 2023
  • ...onc. sulfuric acid<br>Slightly soluble in acetates, [[acetone]], alcohols, amides, aq. acids, [[diethyl ether]]<br>Insoluble in [[ethanol]]
    5 KB (653 words) - 22:02, 5 November 2023
  • The thermal decomposition of amides in the presence of a catalyst will yield hydrogen cyanide gas. An approxima
    10 KB (1,464 words) - 12:40, 26 January 2024
  • ...n. The conjugate bases of these "acids" are superbases, and their "salts" (amides, hydrides, carbides) are ones as well and react with water irreversibly.
    3 KB (535 words) - 21:07, 26 June 2017
  • .../archive/rhodium/chemistry/amide.preparation.html Preparation of Aliphatic Amides]''' ...odium/chemistry/azide2amine.zn-nh4cl.html Reduction of Azides to Amines or Amides With Zinc and Ammonium Chloride as Reducing Agent]'''
    6 KB (941 words) - 16:51, 27 September 2016
  • *Make nitriles from amides
    6 KB (750 words) - 09:43, 15 August 2022
  • [[Category:Metal amides]]
    5 KB (631 words) - 01:20, 30 August 2020
  • ...th excess reagent and/or elevated temperatures, while carboxylic acids and amides are not reduced at all. However, in the presence of elemental [[iodine]], N
    10 KB (1,222 words) - 19:18, 13 August 2023
  • 3 KB (428 words) - 22:37, 10 June 2018
  • ...p://www.sciencemadness.org/talk/viewthread.php?tid=12038 Acid halides from amides]
    2 KB (233 words) - 20:52, 19 May 2019
  • [[Category:Amides]]
    5 KB (501 words) - 20:51, 26 December 2022
  • [[Category:Amides]]
    4 KB (451 words) - 15:11, 4 May 2020
  • [[Category:Amides]]
    4 KB (393 words) - 18:21, 29 February 2020
  • [[Category:Amides]]
    5 KB (552 words) - 17:20, 30 June 2020
  • ...ondary [[amine]]s in [[carbon tetrachloride]] solution to yield perchloric amides:
    5 KB (598 words) - 19:55, 28 August 2020
  • [[Category:Amides]]
    5 KB (559 words) - 19:42, 31 December 2020
  • ...to give the corresponding esters. Similarly, it reacts with amines to give amides. Condensation with [[diethylamine]] for example, yields N,N-diethylbenzamid
    6 KB (662 words) - 10:16, 7 July 2022
  • ...d and black solid products are obtained, suspected to be P-suboxides and P-amides.
    5 KB (644 words) - 23:48, 13 November 2021
  • The preparation of tosyl esters and amides are conducted in the presence of a base, which absorbs hydrogen chloride. T
    5 KB (629 words) - 19:54, 15 September 2022
  • ...borohydride is less reducing 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