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

Wolffenstein–Böters reaction

From Wikipedia, the free encyclopedia

The Wolffenstein–Böters reaction is an organic reaction converting benzene to picric acid by a mixture of aqueous nitric acid and mercury(II) nitrate.[1][2][3]

The reaction, which involves simultaneous nitration and oxidation, was first reported by the German chemists Richard Wolffenstein and Oskar Böters in 1906.[4]

The Wolffenstein-Boters reaction
The Wolffenstein-Boters reaction

According to one series of studies the mercury nitrate first takes benzene to the corresponding nitroso compound and through the diazonium salt to the phenol. The presence of nitrite is essential for the reaction; picric acid formation is prevented when urea, a trap for nitrous acid, is added to the mixture. From then on the reaction proceeds as a regular aromatic nitration.[5][6]

A conceptually related reaction is the Bohn–Schmidt reaction, dating to 1889, which involves the hydroxylation of hydroxyanthraquinone with sulfuric acid and lead or selenium to a polyhydroxylated anthraquinone.

References

  1. ^ Wolffenstein and Boeters, Chem. Abs., I, 489, 1861 (1908); 4, 369 (1910).
  2. ^ Richard Wolffenstein, O. Böters (1913). "Über die katalytische Wirkung des Quecksilbers bei Nitrierungen". Berichte der deutschen chemischen Gesellschaft. 46 (1): 586–589. doi:10.1002/cber.19130460177.
  3. ^ R. Wolffenstein, W. Paar (1913). "Über Nitrierung der Benzoesäure in Gegenwart von Quecksilber". Berichte der deutschen chemischen Gesellschaft. 46 (1): 589–599. doi:10.1002/cber.19130460178.
  4. ^ Wang, Zerong (2010). Wolffenstein–Böters Reaction. doi:10.1002/9780470638859.conrr682. ISBN 9780470638859.
  5. ^ The Mechanism of the Oxynitration of Benzene F. H. Westheimer, Edward Segel, and Richard Schramm J. Am. Chem. Soc.; 1947; 69(4) pp 773 - 785; doi:10.1021/ja01196a011
  6. ^ The Oxynitration of Benzene. I. Studies Relating to the Reaction MechanismsMarvin Carmack, Manuel M. Baizer, G. Richard Handrick, L. W. Kissinger, and Edward H. Specht J. Am. Chem. Soc.; 1947; 69(4) pp 785 - 790; doi:10.1021/ja01196a012

External links

This page was last edited on 27 October 2022, at 19:32
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.