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

Printable Version  
Author: Subject: does any body try these??
sasan
Hazard to Self
**




Posts: 92
Registered: 22-2-2014
Location: TEHRAN / IRAN
Member Is Offline

Mood: Radiative

cool.gif posted on 24-3-2014 at 01:59
does any body try these??


Carbon disulfide is a important reagent in your experiments,and you guys can not purchase it easily and it's not cheap as you know,is it possible:: CCl4 + 2 Na2S (using some heat) = CS2 + 4NaCl ?? using stiometric amounts and distill or decant the carbon disulfide

And does any body try this?::
C2Cl4(Tetrachloroethylene) + 2Na2S =??
View user's profile View All Posts By User
sasan
Hazard to Self
**




Posts: 92
Registered: 22-2-2014
Location: TEHRAN / IRAN
Member Is Offline

Mood: Radiative

[*] posted on 24-3-2014 at 23:17


any ideas?seems nobody had experiences with these...
and some other reactions with H2S::
H2S(g) + NH4HF2(aq) ==??
H2S(g) + C2H5-O-C2H5(l) ==??(maybe diethyl sulfide??)
View user's profile View All Posts By User
Metacelsus
International Hazard
*****




Posts: 2531
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline

Mood: Double, double, toil and trouble

[*] posted on 25-3-2014 at 03:59


The reactions with the chlorinated compounds are plausible, but may not take place at an appreciable rate. Thiophosgene would likely be an intermediate in the reaction with carbon tetrachloride, so watch out.
As for the ammonium bifluoride, the hydrogen sulfide will merely dissolve in the solution and generate a mixture of ions and compounds.
The hydrogen sulfide will just dissolve in the ether. No reaction will occur.

[Edited on 25-3-2014 by Cheddite Cheese]




As below, so above.

My blog: https://denovo.substack.com
View user's profile View All Posts By User
Nicodem
Super Moderator
Thread Moved
25-3-2014 at 08:10

  Go To Top