To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

Electron deficiency

From Wikipedia, the free encyclopedia

In chemistry, electron deficiency (and electron-deficient) is jargon that is used in two contexts: chemical species that violate the octet rule because they have too few valence electrons and species that happen to follow the octet rule but have electron-acceptor properties, forming donor-acceptor charge-transfer salts.

YouTube Encyclopedic

  • 1/3
    Views:
    17 372
    1 083
    1 715
  • Which one is the electron deficient compound ?
  • Identify Electron Deficient Molecule || Top Chemistry Question for NEET
  • Electron Deficiency Syndrome: How to Charge the Human Battery - CHTV 347

Transcription

Octet rule violations

Triphenylborane is classified as electron deficient.

Traditionally, "electron-deficiency" is used as a general descriptor for boron hydrides and other molecules which do not have enough valence electrons to form localized (2-centre 2-electron) bonds joining all atoms.[1] For example, diborane (B2H6) would require a minimum of 7 localized bonds with 14 electrons to join all 8 atoms, but there are only 12 valence electrons.[2] A similar situation exists in trimethylaluminium. The electron deficiency in such compounds is similar to metallic bonding.

Electron-acceptor molecules

Structure of the charge-transfer complex between pyrene with the electron-deficient 1,3,5-trinitrobenzene.[3]

Alternatively, electron-deficiency describes molecules or ions that function as electron acceptors. Such electron-deficient species obey the octet rule, but they have (usually mild) oxidizing properties.[4] 1,3,5-Trinitrobenzene and related polynitrated aromatic compounds are often described as electron-deficient.[5] Electron deficiency can be measured by linear free-energy relationships: "a strongly negative ρ value indicates a large electron demand at the reaction center, from which it may be concluded that a highly electron-deficient center, perhaps an incipient carbocation, is involved."[6]

References

  1. ^ Housecroft, Catherine E.; Sharpe, Alan G. (2005). Inorganic Chemistry (2nd ed.). Pearson Prentice-Hall. p. 326. ISBN 0130-39913-2. An electron-deficient species possesses fewer valence electrons than are required for a localized bonding scheme.
  2. ^ Longuet-Higgins, H.C. (1957). "The structures of electron-deficient molecules". Quarterly Reviews, Chemical Society. 11 (2): 121–133. doi:10.1039/qr9571100121. Retrieved 15 July 2020.
  3. ^ Rather, Sumair A.; Saraswatula, Viswanadha G.; Sharada, Durgam; Saha, Binoy K. (2019). "Influence of molecular width on the thermal expansion in solids". New Journal of Chemistry. 43 (44): 17146–17150. doi:10.1039/C9NJ04888J. S2CID 208752583.
  4. ^ Stalder, Romain; Mei, Jianguo; Graham, Kenneth R.; Estrada, Leandro A.; Reynolds, John R. (2014). "Isoindigo, a Versatile Electron-Deficient Unit for High-Performance Organic Electronics". Chemistry of Materials. 26: 664–678. doi:10.1021/cm402219v.
  5. ^ Goetz, Katelyn P.; Vermeulen, Derek; Payne, Margaret E.; Kloc, Christian; McNeil, Laurie E.; Jurchescu, Oana D. (2014). "Charge-Transfer Complexes: New Perspectives on an Old Class of Compounds". J. Mater. Chem. C. 2 (17): 3065–3076. doi:10.1039/C3TC32062F.
  6. ^ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 412, ISBN 978-0-471-72091-1
This page was last edited on 12 November 2023, at 01:20
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.