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

From Wikipedia, the free encyclopedia

Ethyl azide
Skeletal formula of ethyl azide
Ball-and-stick model of the ethyl azide molecule
Names
Preferred IUPAC name
Azidoethane
Other names
Ethane, azido-; 1-Azidoethane
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C2H5N3/c1-2-4-5-3/h2H2,1H3 ☒N
    Key: UCSVJZQSZZAKLD-UHFFFAOYSA-N ☒N
  • InChI=1/C2H5N3/c1-2-4-5-3/h2H2,1H3
    Key: UCSVJZQSZZAKLD-UHFFFAOYAG
  • [N-]=[N+]=N/CC
Properties
CH3CH2N3
Molar mass 71.083 g·mol−1
Appearance liquid
Boiling point 50
Explosive data
Shock sensitivity High
Friction sensitivity High
Thermochemistry
266.872
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Harmful, Explosive
Related compounds
Related compounds
Hydrazoic acid, Chlorine azide, Methyl azide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Ethyl azide (CH3CH2N3) is an explosive compound sensitive to rapid heating, shock or impact. It has exploded when heated to room temperature.[1][2] When heated to decomposition it emits toxic fumes of NOx.[3][4]

It is irritating to eyes, respiratory system and skin.

YouTube Encyclopedic

  • 1/1
    Views:
    31 636
  • Organic Chemistry 51B. Lecture 02. Alcohols, Ethers, and Epoxides Part 1.

Transcription

Uses

Ethyl azide is used for organic synthesis.

References

  1. ^ Campbell, H. C.; Rice, O. K. (1935). "The Explosion of Ethyl Azide". Journal of the American Chemical Society. 57 (6): 1044–1050. doi:10.1021/ja01309a019.
  2. ^ Rice, O. K.; Campbell, H. C. (1939). "The Explosion of Ethyl Azide in the Presence of Diethyl Ether". The Journal of Chemical Physics. 7 (8): 700–709. Bibcode:1939JChPh...7..700R. doi:10.1063/1.1750516.
  3. ^ Rice, O. K. (1940). "The Role of Heat Conduction in Thermal Gaseous Explosions". The Journal of Chemical Physics. 8 (9): 727–733. Bibcode:1940JChPh...8..727R. doi:10.1063/1.1750808.
  4. ^ Costa Cabral, B. J.; Costa, M. L.; Almoster Ferreira, M. A. (2010). "ChemInform Abstract: Molecular Structure and Ionization Energies of Azides: An ab initio Study of Hydrazoic Acid, Methyl Azide and Ethyl Azide". ChemInform. 24 (37): no. doi:10.1002/chin.199337053.
This page was last edited on 13 August 2023, at 10:41
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.