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

Printable Version  
Author: Subject: Oxidizing alcohols for beginners - Making oxidizing agent
cnidocyte
Hazard to Others
***




Posts: 214
Registered: 7-7-2010
Member Is Offline

Mood: No Mood

[*] posted on 13-9-2010 at 14:21
Oxidizing alcohols for beginners - Making oxidizing agent


I wanna put a bit of my organic chem theory into practice and I wanna start with oxidizing alcohols since methanol, ethanol and isopropanol are cheap and OTC. I wanna make the oxidizing agent myself from OTC compounds but I don't know what would be the easiest oxidizer to make. I wanna avoid chromates and dichromates since they're so toxic. I could make KMnO4 that from MnO2. Would that be the simplest oxidizing agent to make or is there an easier one to make?
View user's profile View All Posts By User
mnick12
Hazard to Others
***




Posts: 404
Registered: 30-12-2009
Location: In the lab w/ Dr. Evil
Member Is Offline

Mood: devious

[*] posted on 13-9-2010 at 16:02


Well it all depends on what you have available as well as what you want. My question is, what is your desired product? There are lots of possibilities, for example ethanol can be fully oxidized to acetic acid in a number of different ways. But with a milder oxidizing agent ethanol would be oxidized to acetaldehyde. So are you interested in aldehydes carboxylic acids, or perhaps both?

Now an alcohol such as isopropanol would not be oxidized to an alehyde, instead you would end up with a ketone (acetone). So in terms of economy some things are much cheaper to buy (formaldehyde,formic acid, acetic acid, acetone), the only one which may be worth pursuing is acetaldehyde. But thats your decision to make.

So mabe a good idea would be decide exactly what your target chemical is, then ask for help making that particular chemical.
View user's profile View All Posts By User

  Go To Top