The Wöhler synthesis is the conversion of ammonium cyanate into urea. This chemical reaction was described in 1828 by Friedrich Wöhler.[1] It is often cited as the starting point of modern organic chemistry. Although the Wöhler reaction concerns the conversion of ammonium cyanate, this salt appears only as an (unstable) intermediate. Wöhler demonstrated the reaction in his original publication with different sets of reactants: a combination of cyanic acid and ammonia, a combination of silver cyanate and ammonium chloride, a combination of lead cyanate and ammonia and finally from a combination of mercury cyanate and cyanatic ammonia (which is again cyanic acid with ammonia).[2]
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Wohler reaction and its Mechanism
Transcription
Modified versions of the Wöhler synthesis
The reaction can be demonstrated by starting with solutions of potassium cyanate and ammonium chloride which are mixed, heated and cooled again. An additional proof of the chemical transformation is obtained by adding a solution of oxalic acid which forms urea oxalate as a white precipitate.[3]
Alternatively the reaction can be carried out with lead cyanate and ammonia.[4] The actual reaction taking place is a double displacement reaction to form ammonium cyanate:
- Pb(OCN)2 + 2 NH3 + 2 H2O → Pb(OH)2 + 2NH4(OCN)
Ammonium cyanate decomposes to ammonia and cyanic acid which in turn react to produce urea:
- NH4(OCN) → NH3 + HOCN ⇌ (NH2)2CO
Complexation with oxalic acid drives this chemical equilibrium to completion.
Debate
It is disputed that Wöhler's synthesis sparked the downfall of the theory of vitalism, which states that organic matter possessed a certain vital force common to all living things. Prior to the Wöhler synthesis, the work of John Dalton and Jöns Jacob Berzelius had already convinced chemists that organic and inorganic matter obey the same chemical laws. It took until 1845 when Kolbe reported another inorganic – organic conversion (of carbon disulfide to acetic acid) before vitalism started to lose support.[5][6] Wöhler also did not, as some textbooks have claimed, act as a "crusader" against vitalism. A 2000 survey by historian Peter Ramberg found that 90% of chemical textbooks repeat some version of the Wöhler myth.[7]
References
- ^ Friedrich Wöhler (1828). "Ueber künstliche Bildung des Harnstoffs". Annalen der Physik und Chemie. 88 (2): 253–256
- ^ Cohen, Paul S.; Cohen, Stephen M. (1996). "Wöhler's Synthesis of Urea: How do the Textbooks Report It?". Journal of Chemical Education. 73 (9): 883. doi:10.1021/ed073p883.
- ^ Tóth, Zoltán (1996). "A demonstration of Wöhler's experiment: Preparation of urea from ammonium chloride and potassium cyanate". Journal of Chemical Education. 73 (6): 539. Bibcode:1996JChEd..73..539T. doi:10.1021/ed073p539.2.
- ^ Batchelor, James D.; Carpenter, Everett E.; Holder, Grant N.; Eagle, Cassandra T.; Fielder, Jon; Cummings, Jared (1998). "Recreation of Wöhler's Synthesis of Urea: An Undergraduate Organic Laboratory Exercise". The Chemical Educator. 3 (6): 1–7. doi:10.1007/s00897980271a. S2CID 95650676.
- ^ "Introduction", Newton's Apple and Other Myths about Science, Harvard University Press, pp. 59–66, 31 December 2015, retrieved 29 July 2022,
Myth 7. That Friedrich Wöhler's Synthesis of Urea in 1828 Destroyed Vitalism and Gave Rise to Organic Chemistry
- ^ Newton’s Apple and Other Myths about Science. Harvard University Press. 4 November 2015. doi:10.4159/9780674089167. ISBN 978-0-674-08916-7.
- ^ Ramberg, Peter J. (2000). "The Death of Vitalism and the Birth of Organic Chemistry: Wohler's Urea Synthesis and the Disciplinary Identity of Organic Chemistry". Ambix. 47 (3): 170–195. doi:10.1179/amb.2000.47.3.170. PMID 11640223. S2CID 44613876.
This page was last edited on 14 February 2024, at 23:52