Svoboda | Graniru | BBC Russia | Golosameriki | Facebook

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-Phenylhexane

From Wikipedia, the free encyclopedia

2-Phenylhexane
Names
Preferred IUPAC name
(Hexan-2-yl)benzene
Other names
2-Phenylhexane
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C12H18/c1-3-4-8-11(2)12-9-6-5-7-10-12/h5-7,9-11H,3-4,8H2,1-2H3 checkY
    Key: CYBSWFUWEZFKNJ-UHFFFAOYSA-N checkY
  • InChI=1/C12H18/c1-3-4-8-11(2)12-9-6-5-7-10-12/h5-7,9-11H,3-4,8H2,1-2H3
    Key: CYBSWFUWEZFKNJ-UHFFFAOYAV
  • CCCCC(C)C1=CC=CC=C1
  • c1ccccc1C(CCCC)C
Properties
C12H18
Molar mass 162.276 g·mol−1
Density 0.858 g/ml
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-Phenylhexane is an aromatic hydrocarbon. It can be produced by a Friedel-Crafts alkylation between 1-chlorohexane and benzene.,[1] or by the reaction of benzene and 1-hexene with various acid catalysts such as antimony pentafluoride,[2] scandium(III) triflate,[3] and phosphoric acid.[4]

YouTube Encyclopedic

  • 1/1
    Views:
    424 317
  • Aromatics and Cyclic Compounds - Crash Course Chemistry #42

Transcription

References

  1. ^ Organic Chemistry Marye Anne Fox, James K. Whitesell (Google books)
  2. ^ Zhurnal Organicheskoi Khimii, 17(7), 1505-11; 1981
  3. ^ Choong Eui Song; Woo Ho Shimb; Eun Joo Roha; Jung Hoon Choi (2000). "Scandium(III) triflate immobilised in ionic liquids: a novel and recyclable catalytic system for Friedel-Crafts alkylation of aromatic compounds with alkenes". Chem. Commun. 2000 (17): 1695–1696. doi:10.1039/b005335j.
  4. ^ Industrial & Engineering Chemistry Research, 46(9), 2902-2906; 2007


Stub icon

This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it.

Stub icon

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

This page was last edited on 25 March 2023, at 22:19
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