Chemistry:Dibromoacetylene
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| Preferred IUPAC name
1,2-Dibromoethyne[1] | |
| Identifiers | |
3D model (JSmol)
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C2Br2 | |
| Molar mass | 183.830 g·mol−1 |
| Melting point | −16.5 °C (2.3 °F; 256.6 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Dibromoacetylene is a molecular chemical compound containing acetylene, with its hydrogen substituted by bromine.
Production
Dibromoacetylene can be made by reacting 1,1,2-tribromoethylene with potassium hydroxide. This method has a danger of causing explosions.[2]
Another way is to react acetylene with phenyl lithium (at −50 °C) to make lithium acetylide, which then reacts with bromine to yield the product.[3]
Yet another way is to react acetylene with sodium hypobromite NaOBr.[4]
Properties
Dibromoacetylene is explosive and sensitive to air.[4] Its appearance is a clear water like liquid. It has a sweetish smell, but makes a white fume in air that then smells like ozone, possibly because it forms ozone.[2] Dibromoacetylene is lachrymatory.[2]
Dibromoacetylene can be polymerised to polydibromoacetylene using catalysts like titanium tetrachloride and triethylaluminium. Polydibromoacetylene is black, electrically conducting, and stable in air to over 200 °C.[4]
The infrared spectrum has absorption at 2185 cm−1 due to symmetrical stretching on the C≡C bond, 832 cm−1 asymmetrical stretch on C-Br bond, 311 cm−1 bending on Z shape BrCC, 267 symmetrical stretch on all bonds, and 167 cm−1 for C-shaped bending.[2]
Reactions
In air dibromoacetylene spontaneously inflames producing black sooty smoke and a red flame. When heated, it explodes, yielding carbon and other substances. A slower reaction with oxygen and water, yields oxalic acid and hydrobromic acid and other bromine containing substances. A reaction with hydrogen iodide yields dibromoiodoethylene. Dibromoacetylene reacts with bromine to yield tetrabromoethene.[5]
Dibromoacetylene reacts with Apiezon L, which is used as a vacuum grease in distillation, so its use is unsuitable with this chemical.[2]
References
- ↑ "Dibromoacetylene". National Library of Medicine. https://pubchem.ncbi.nlm.nih.gov/compound/61169.
- ↑ 2.0 2.1 2.2 2.3 2.4 Kloster-Jenson, Else (1971). "Preparation and physical characterization of pure hetero and homo dihaloacetylenes". Tetrahedron 27 (1): 33–49. doi:10.1016/S0040-4020(01)92395-6.
- ↑ Meijere, Armin de (2014) (in en). Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 24: Three Carbon-Heteroatom Bonds: Ketene Acetals and Yne-X Compounds. Georg Thieme Verlag. pp. 1191–1192. ISBN 978-3-13-178171-0. https://books.google.com/books?id=j-eIAwAAQBAJ&pg=PA1191.
- ↑ 4.0 4.1 4.2 Leben, S.; Janevski, A.; Šebenik, A.; Osredkar, U. (May 1992). "The synthesis and characterization of polydibromoacetylene". Polymer Bulletin 28 (3): 287–292. doi:10.1007/BF00294824. http://eprints.ugd.edu.mk/6118/1/__ugd.edu.mk_private_UserFiles_aco.janevski_Desktop_trudovi_statii_The%20Synthesis%20and%20Characterization%20of%20Polydibromoacetylene.pdf.
- ↑ Sartori, Mario (1939). The War Gases Chemistry and Analysis. New York: D. Van Nostrand Co., Inc.. p. 51. https://archive.org/stream/The_War_Gases_Chemistry_and_Analysis_Sartori/The_War_Gases_Chemistry_and_Analysis_Sartori_djvu.txt.
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