Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Q regarding tetraalkylammoniums
moo
Harmless
*




Posts: 2
Registered: 17-2-2011
Member Is Offline

Mood: No Mood

cool.gif posted on 26-2-2011 at 15:18
Q regarding tetraalkylammoniums


Hi Science Madness community, nice to meet you. I have been a reader here for several years now, and am only now joining. I hope to be able to ask good questions that yield answers to help other readers and to jog the minds of the knowledgeable.:D I may be able to share experience on some matters, but am generally here to learn. I thank you for your time and eyes!

So then the question of this post is:

Are tetraalkylammonium hydroxides hard to make or aquire/request?

Such as TBAOH?

And, what uses would a chemist have for TBAOH, instead of say potash flakes (KOH) or NaOH?

View user's profile View All Posts By User
Maja
Hazard to Others
***




Posts: 143
Registered: 27-2-2006
Member Is Offline

Mood: No Mood

[*] posted on 26-2-2011 at 15:39


http://www.sciencemadness.org/talk/viewthread.php?tid=9496#p...
try searching next time yourself :)
View user's profile View All Posts By User
moo
Harmless
*




Posts: 2
Registered: 17-2-2011
Member Is Offline

Mood: No Mood

[*] posted on 26-2-2011 at 16:16


Thanks. *wipes a piece of embarrassed sweat*
View user's profile View All Posts By User
kmno4
International Hazard
*****




Posts: 1497
Registered: 1-6-2005
Location: Silly, stupid country
Member Is Offline

Mood: No Mood

[*] posted on 27-2-2011 at 00:30


Quote: Originally posted by moo  

So then the question of this post is:
Are tetraalkylammonium hydroxides hard to make or aquire/request?
Such as TBAOH?
And, what uses would a chemist have for TBAOH, instead of say potash flakes (KOH) or NaOH?

Solutions of TBAOH are comercially available.
TBAOH can be made from TBAChal and Ag2O (+ H donor), possibly also from TBAHSO4 and Ba(OH)2.
Try this:
Take nitrobenzene and add to it small amount of solid NaOH.
If nitrobenzene is pure - nothing happens (at room temp).
Next, add small amount of TBACl (or similar).
Immediately deep red colour of Meisenheimer complex appears.
TBAOH is very strong and soluble base, it attacks even such inert reagent like mononitrobenzene.
View user's profile View All Posts By User
smuv
National Hazard
****




Posts: 842
Registered: 2-5-2007
Member Is Offline

Mood: Jingoistic

[*] posted on 27-2-2011 at 12:33


TBAOH can also be prepared from the chloride via NaOH in alcohol. The sodium chloride precipitates.
View user's profile View All Posts By User

  Go To Top