Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Polarizability
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
==Atomic and molecular polarizability== Generally, polarizability increases as the volume occupied by electrons increases.<ref name="anslyn"/> In atoms, this occurs because larger atoms have more loosely held electrons in contrast to smaller atoms with tightly bound electrons.<ref name="anslyn"/><ref name="Schwerdtfeger">{{cite book |last1=Schwerdtfeger |first1=Peter |title=Atomic Static Dipole Polarizabilities |publisher=[[IOS Press]] |year=2006 |editor=G. Maroulis |chapter=Computational Aspects of Electric Polarizability Calculations: Atoms, Molecules and Clusters}}[http://www.worldscibooks.com/etextbook/p464/p464_chap01.pdf]{{dead link|date=January 2018|bot=InternetArchiveBot|fix-attempted=yes}}</ref> On rows of the [[periodic table]], polarizability therefore decreases from left to right.<ref name="anslyn"/> Polarizability increases down on columns of the periodic table.<ref name="anslyn"/> Likewise, larger molecules are generally more polarizable than smaller ones. Water is a very [[chemical polarity|polar]] molecule, but [[alkanes]] and other [[hydrophobic]] molecules are more polarizable. Water with its permanent dipole is less likely to change shape due to an external electric field. Alkanes are the most polarizable molecules.<ref name="anslyn"/> Although [[alkenes]] and [[arenes]] are expected to have larger polarizability than alkanes because of their higher reactivity compared to alkanes, alkanes are in fact more polarizable.<ref name="anslyn"/> This results because of alkene's and arene's more electronegative sp<sup>2</sup> carbons to the alkane's less electronegative sp<sup>3</sup> carbons.<ref name="anslyn"/> Ground state electron configuration models often describe molecular or bond polarization during [[chemical reaction]]s poorly, because [[reactive intermediate]]s may be excited, or be the minor, alternate structures in a [[chemical equilibrium]] with the initial reactant.<ref name="anslyn">{{cite book |last1=Anslyn |first1=Eric |title=Modern Physical Organic Chemistry |last2=Dougherty |first2=Dennis |author-link2=Dennis A. Dougherty |publisher=University Science |year=2006 |isbn=978-1-891389-31-3}}[https://books.google.com/books?id=gY-Sxijk_tMC&dq=organic+chemistry+polarizability&pg=PA25]</ref>
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)