World Library  
Flag as Inappropriate
Email this Article


Article Id: WHEBN0000515683
Reproduction Date:

Title: Carbanion  
Author: World Heritage Encyclopedia
Language: English
Subject: Birch reduction, Anionic addition polymerization, Ylide, E1cB-elimination reaction, Azomethine ylide
Collection: Anions, Reactive Intermediates
Publisher: World Heritage Encyclopedia



A carbanion is an anion in which carbon has an unshared pair of electrons and bears a negative charge usually with three substituents for a total of eight valence electrons.[1] The carbanion exists in a trigonal pyramidal geometry. Formally, a carbanion is the conjugate base of a carbon acid.

R3C-H + BR3C + H-B

where B stands for the base. A carbanion is one of several organic chemistry.


  • Theory 1
  • Carbon acids 2
  • Chiral carbanions 3
  • History 4
  • External links 5
  • See also 6
  • References 7


A carbanion is a nucleophile. The stability and reactivity of a carbanion is determined by several factors. These include

  1. The inductive effect. Electronegative atoms adjacent to the charge will stabilize the charge;
  2. Hybridization of the charge-bearing atom. The greater the s-character of the charge-bearing atom, the more stable the anion;
  3. The extent of conjugation of the anion. Resonance effects can stabilize the anion. This is especially true when the anion is stabilized as a result of aromaticity.

A carbanion is a Grignard reaction or in alkyl lithium chemistry. Stable carbanions do however exist. In 1984 Olmstead presented the lithium crown ether salt of the triphenylmethyl carbanion from triphenylmethane, n-butyllithium and 12-crown-4 at low temperatures:[2]

Formation of the triphenylmethane anion

Adding n-butyllithium to triphenylmethane in THF at low temperatures followed by 12-crown-4 results in a red solution and the salt complex precipitates at −20 °C. The central C-C bond lengths are 145 pm with the phenyl ring propelled at an average angle of 31.2°. This propeller shape is less pronounced with a tetramethylammonium counterion .[3]

One tool for the detection of carbanions in solution is proton NMR.[4] A spectrum of cyclopentadiene in DMSO shows four vinylic protons at 6.5 ppm and two methylene bridge protons at 3 ppm whereas the cyclopentadienyl anion has a single resonance at 5.50 ppm.

Carbon acids

Any molecule containing a C-H can lose a proton forming the carbanion. Hence any hydrocarbon containing C-H bonds can be considered an acid with a corresponding pKa value. Methane is certainly not an acid in its classical meaning yet its estimated pKa is 56. Compare this to acetic acid with pKa 4.76. The same factors that determine the stability of the carbanion also determine the order in pKa in carbon acids. These values are determined for the compounds either in water in order to compare them to ordinary acids, in dimethyl sulfoxide in which the majority of carbon acids and their anions are soluble or in the gas phase. With DMSO the acidity window for solutes is limited to its own pKa of 35.5.

name formula structural formula pKa
Methane CH4 ~ 56
Ethane C2H6 ~ 50
Anisole C7H8O ~ 49
Cyclopentane C5H10 ~ 45
Propene C3H6 ~ 44
Benzene C6H6 ~ 43
Toluene C6H5CH3 ~ 43
Dimethyl sulfoxide (CH3)2SO 35.5
Diphenylmethane C13H12 32.3
Aniline C6H5NH2 30.6
Triphenylmethane C19H16 30.6
Xanthene C13H10O 30
Ethanol C2H5OH 29.8
Phenylacetylene C8H6 28.8
Thioxanthene C13H10S 28.6
Acetone C3H6O 26.5
Acetylene C2H2 25
Benzoxazole C7H5NO 24.4
Fluorene C13H10 22.6
Indene C9H8 20.1
Cyclopentadiene C5H6 18
Malononitrile C3H2N2 11.2
Hydrogen cyanide HCN 9.2
Acetylacetone C5H8O2 8.95
Dimedone C8H12O2 5.23
Meldrum's acid C6H8O4 4.97
Acetic acid CH3COOH 4.76
Barbituric acid C4H2O3(NH)2 4.01
Trinitromethane HC(NO2)3 0.17
Fulminic acid HCNO -1.07
Carborane acid HCHB11Cl11 -9
Table 1. Carbon acid acidities in pKa in DMSO [5]. Reference acids in bold.

Note that the anions formed by ionization of acetic acid, ethanol, and aniline are not carbanions.

Starting from methane in table 1, the acidity increases:

  • when the anion is aromatic, either because the added electron causes the anion to become aromatic (as in indene and cyclopentadiene), or because the negative charge on carbon can be delocalized over several already-aromatic rings (as in triphenylmethane or carborane acid).
  • when the carbanion is surrounded by strongly electronegative groups, through the partial neutralisation of the negative charge (as in malononitrile).
  • when the carbanion is immediately next to a carbonyl group. The α-protons of aldol reaction.

Chiral carbanions

With the organolithium compounds.

The first ever evidence for the existence of chiral organolithium compounds was obtained in 1950. Reaction of chiral 2-iodooctane with sec-butyllithium in petroleum ether at −70 °C followed by reaction with dry ice yielded mostly racemic 2-methylbutyric acid but also an amount of optically active 2-methyloctanoic acid which could only have formed from likewise optical active 2-methylheptyllithium with the carbon atom linked to lithium the carbanion:[6]

On heating the reaction to 0 °C the optical activity is lost. More evidence followed in the 1960s. A reaction of the cis isomer of 2-methylcyclopropyl bromide with sec-butyllithium again followed by carboxylation with dry ice yielded cis-2-methylcyclopropylcarboxylic acid. The formation of the trans isomer would have indicated that the intermediate carbanion was unstable.[7]

In the same manner the reaction of (+)-(S)-l-bromo-l-methyl-2,2-diphenylcyclopropane with n-butyllithium followed by quench with methanol resulted in product with retention of configuration:[8]

Optical Stability of 1-Methyl-2,2-diphenylcyclopropyllithium

Of recent date are chiral methyllithium compounds:[9]

Chiral -Oxy-[2H1]methyllithiums, Bu stands for butyl, i-Pr stands for isopropyl

The phosphate 1 contains a chiral group with a hydrogen and a deuterium substituent. The stannyl group is replaced by lithium to intermediate 2 which undergoes a phosphate-phosphorane rearrangement to phosphorane 3 which on reaction with acetic acid gives alcohol 4. Once again in the range of −78 °C to 0 °C the chirality is preserved in this reaction sequence.[10]


A carbanionic structure first made an appearance in the reaction mechanism for the CNa3Ph) [12] and in 1914 he demonstrated how triarylmethyl radicals could be reduced to carbonions by alkali metals [13] The phrase carbanion was introduced by Wallis and Adams in 1933 as the negatively charged counterpart of the carbonium ion [14][15]

External links

  • Large database of Bordwell pKa values at Link
  • Large database of Bordwell pKa values at Link

See also


  1. ^ Organic Chemistry - Robert Thornton Morrison, Robert Neilson Boyd
  2. ^ The isolation and x-ray structures of lithium crown ether salts of the free phenyl carbanions [CHPh2]- and [CPh3]- Marilyn M. Olmstead, Philip P. Power; J. Am. Chem. Soc.; 1985; 107(7); 2174-2175. doi:10.1021/ja00293a059
  3. ^ Harder, S. (2002). "Schlenk's Early "Free" Carbanions". Chemistry - A European Journal 8 (14): 3229–3229.  
  4. ^ A Simple and Convenient Method for Generation and NMR Observation of Stable Carbanions. Hamid S. Kasmai Journal of Chemical Education • Vol. 76 No. 6 June 1999
  5. ^ Equilibrium acidities in dimethyl sulfoxide solution Frederick G. Bordwell Acc. Chem. Res.; 1988; 21(12) pp 456 - 463; doi:10.1021/ar00156a004
  6. ^ FORMATION OF OPTICALLY ACTIVE 1-METHYLHEPTYLLITHIUM Robert L. Letsinger J. Am. Chem. Soc.; 1950; 72(10) pp 4842 - 4842; doi:10.1021/ja01166a538
  7. ^ The Configurational Stability of cis- and trans-2-Methylcyclopropyllithium and Some Observations on the Stereochemistry of their Reactions with Bromine and Carbon Dioxide Douglas E. Applequist and Alan H. Peterson J. Am. Chem. Soc.; 1961; 83(4) pp 862 - 865; doi:10.1021/ja01465a030
  8. ^ Cyclopropanes. XV. The Optical Stability of 1-Methyl-2,2-diphenylcyclopropyllithium H. M. Walborsky, F. J. Impastato, and A. E. Young J. Am. Chem. Soc.; 1964; 86(16) pp 3283 - 3288; doi:10.1021/ja01070a017
  9. ^ Preparation of Chiral -Oxy-[2H1]methyllithiums of 99% ee and Determination of Their Configurational Stability Dagmar Kapeller, Roland Barth, Kurt Mereiter, and Friedrich Hammerschmidt J. Am. Chem. Soc.; 2007; 129(4) pp 914 - 923; (Article) doi:10.1021/ja066183s
  10. ^ Enantioselectivity determined by NMR spectroscopy after derivatization with Mosher's acid
  11. ^ Clarke, R. W. L.; Lapworth, A. (1907). "LXV.?An extension of the benzoin synthesis". Journal of the Chemical Society, Transactions 91: 694.  
  12. ^ Schlenk, W.; Weickel, T.; Herzenstein, A. (1910). "Ueber Triphenylmethyl und Analoga des Triphenylmethyls in der Biphenylreihe. [Zweite Mittheilung über „Triarylmethyle”.]". Justus Liebig's Annalen der Chemie 372: 1.  
  13. ^ Schlenk, W.; Marcus, E. (1914). "Über Metalladditinen an freie organische Radikale. (Über Triarylmethyle. XII.)". Berichte der deutschen chemischen Gesellschaft 47 (2): 1664.  
  14. ^ Wallis, E. S.; Adams, F. H. (1933). "The Spatial Configuration of the Valences in Tricovalent Carbon Compounds1". Journal of the American Chemical Society 55 (9): 3838.  
  15. ^ Tidwell, T. T. (1997). "The first century of physical organic chemistry: A prologue". Pure and Applied Chemistry 69 (2): 211–214.  
This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.

Copyright © World Library Foundation. All rights reserved. eBooks from Project Gutenberg are sponsored by the World Library Foundation,
a 501c(4) Member's Support Non-Profit Organization, and is NOT affiliated with any governmental agency or department.