• Organosodium chemistry is the chemistry of organometallic compounds containing a carbon to sodium chemical bond. The application of organosodium compounds...
    11 KB (1,261 words) - 00:12, 27 August 2023
  • Thumbnail for Organometallic chemistry
    organometallic chemistry include: Period 2 elements: organolithium chemistry, organoberyllium chemistry, organoborane chemistry Period 3 elements: organosodium chemistry...
    31 KB (3,140 words) - 14:35, 7 August 2024
  • Alkynylation (category Organometallic chemistry)
    acetylene and acetone. Alkylation Methylation Organolithium reagent Organosodium chemistry Sonogashira coupling Glaser coupling Cadiot–Chodkiewicz coupling...
    12 KB (1,249 words) - 07:49, 9 May 2024
  • Thumbnail for Alkylation
    such as Grignard (organomagnesium), organolithium, organocopper, and organosodium reagents. These compounds typically can add to an electron-deficient...
    15 KB (1,651 words) - 13:59, 24 August 2024
  • Thumbnail for Sodium tetraphenylborate
    Na+-phenyl interactions. As such the salt could be classified as an organosodium compound. Addition of sodium tetraphenylborate to a solution of a tertiary...
    6 KB (631 words) - 00:31, 19 March 2024
  • stable in ionic compounds. It can also form intermetallic compounds and organosodium compounds. Sodium compounds are often soluble in water. Metallic sodium...
    14 KB (1,527 words) - 02:23, 13 August 2023
  • halide, increasing the probability that the alkyl halide will form the organosodium bond first and thus act more effectively as a nucleophile toward the...
    9 KB (915 words) - 00:40, 20 November 2023
  • Thumbnail for Sodium
    cryptands to solutions of sodium in ammonia via disproportionation. Many organosodium compounds have been prepared. Because of the high polarity of the C-Na...
    70 KB (8,197 words) - 02:14, 25 August 2024
  • Thumbnail for Alkali metal
    alkali metals are predominantly ionic. The application of organosodium compounds in chemistry is limited in part due to competition from organolithium...
    214 KB (23,508 words) - 15:09, 23 August 2024
  • anion sodium naphthalene to styrene. The results in the formation of an organosodium species, which rapidly added styrene to form a "two – ended living polymer...
    16 KB (1,844 words) - 03:22, 5 August 2024
  • Thumbnail for N-Butylsodium
    N-Butylsodium (category Organosodium compounds)
    organometallic compound with the idealized formula NaC4H9. Like other simple organosodium compounds, it is polymeric and highly basic. In contrast to n-butyllithium...
    5 KB (328 words) - 08:44, 17 June 2023
  • Thumbnail for Sodium methylsulfinylmethylide
    Sodium methylsulfinylmethylide (category Organosodium compounds)
    base of dimethyl sulfoxide. This unusual salt has some uses in organic chemistry as a base and nucleophile. Since the first publication in 1965 by Corey...
    7 KB (507 words) - 04:24, 22 March 2024
  • and [NMe4]+[PhCH2]−, respectively, by metathesis of the corresponding organosodium reagent with tetramethylammonium chloride. Since tetramethylammonium...
    32 KB (3,469 words) - 20:32, 22 July 2024
  • Thumbnail for Sodium cyclopentadienide
    Sodium cyclopentadienide (category Organosodium compounds)
    Sodium cyclopentadienide is an organosodium compound with the formula C5H5Na. The compound is often abbreviated as NaCp, where Cp− is the cyclopentadienide...
    7 KB (725 words) - 02:13, 19 June 2024
  • Thumbnail for Sodium naphthalene
    Sodium naphthalene (category Organosodium compounds)
    reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. When isolated, it invariably crystallizes...
    5 KB (420 words) - 11:50, 1 July 2024
  • 1021/jo01348a012. However, see Wurtz coupling for cases where an in situ generated organosodium reagent reacts with an alkyl halide. Lipshutz, Bruce H. (2002). Schlosser...
    11 KB (1,505 words) - 20:21, 12 July 2024