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.

How to transfigure the Wikipedia

Would you like Wikipedia to always look as professional and up-to-date? We have created a browser extension. It will enhance any encyclopedic page you visit with the magic of the WIKI 2 technology.

Try it — you can delete it anytime.

Install in 5 seconds
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.
Great Wikipedia has got greater.
.
Leo
Newton
Brights
Milds

2-Bromohexane

From Wikipedia, the free encyclopedia

2-Bromohexane
Skeletal formula of 2-bromohexane
Names
Preferred IUPAC name
2-Bromohexane[1]
Other names
2-Hexyl bromide[citation needed]
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.020.159 Edit this at Wikidata
EC Number
  • 222-173-3
UNII
  • InChI=1S/C6H13Br/c1-3-4-5-6(2)7/h6H,3-5H2,1-2H3 checkY
    Key: NEBYCXAKZCQWAW-UHFFFAOYSA-N checkY
  • CCCCC(C)Br
Properties
C6H13Br
Molar mass 165.074 g·mol−1
Appearance Colorless liquid
Density 1.1891 g mL−1
Boiling point 143 °C (289 °F; 416 K)
Hazards
Flash point 47 °C (117 °F; 320 K)
Related compounds
Related alkanes
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 ?)

2-Bromohexane is the organobromine compound with the formula CH3CH(Br)(CH2)3CH3. It is a colorless liquid. The compound is chiral. Most 2-bromoalkanes are prepared by addition of hydrogen bromide to the 1-alkene. Markovnikov addition proceeds in the absence of free-radicals, i.e. give the 2-bromo derivatives.[2]

YouTube Encyclopedic

  • 1/3
    Views:
    22 563
    1 472
    40 699
  • Make Alkyl Halides Bromoethane and Bromohexane
  • Haloalkanes1c: 26 isomers of C6H13Br
  • SN1 SN2 E1 E2 Practice Problems, Reagents, Reaction Mechanisms Made Easy

Transcription

References

  1. ^ "2-BROMOHEXANE - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 27 March 2005. Identification. Retrieved 18 June 2012.
  2. ^ Dagani, M. J.; Barda, H. J.; Benya, T. J.; Sanders, D. C. "Bromine Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_405. ISBN 978-3527306732.
Stub icon

This article about an organic halide is a stub. You can help Wikipedia by expanding it.

This page was last edited on 27 September 2023, at 09:20
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.
Contact WIKI 2
Introduction
Terms of Service
Privacy Policy