death11284
30th September 2008, 03:50 AM
Ok first of all butyric acid is simply butanoic acid...for some reason the IUPAC chose to name it funny...
Anyways the structure is simple...
OH
|
C-C-C-C=O
Yes I'm aware it resembles a cock.
So my idea...I have all the necessary materials.
Using a refilling hose for a lighter, butane from said lighter is bubbled through highly concentrated hydrogen peroxide, this SHOULD oxidize it. I am not sure the exact effect this will have, and I can't find anything on it on google. Would this result in the double bonded oxygen listed above?
After this adding the hydroxide group...I was thinking of adding a metal hydroxide high on the activity table at 1st (such as NaOH, or MgOH) however it seems that this would simply kick out a hydrogen in favor of said high activity metal...
Any ideas on this?
The butyric acid is just for experimenting, I want to experiment with some esters, I especially want to find the ester of rancid butter, reputably so horrible as to induce vomiting. Though the butyric acid is pretty bad on it's own...
Anyways the structure is simple...
OH
|
C-C-C-C=O
Yes I'm aware it resembles a cock.
So my idea...I have all the necessary materials.
Using a refilling hose for a lighter, butane from said lighter is bubbled through highly concentrated hydrogen peroxide, this SHOULD oxidize it. I am not sure the exact effect this will have, and I can't find anything on it on google. Would this result in the double bonded oxygen listed above?
After this adding the hydroxide group...I was thinking of adding a metal hydroxide high on the activity table at 1st (such as NaOH, or MgOH) however it seems that this would simply kick out a hydrogen in favor of said high activity metal...
Any ideas on this?
The butyric acid is just for experimenting, I want to experiment with some esters, I especially want to find the ester of rancid butter, reputably so horrible as to induce vomiting. Though the butyric acid is pretty bad on it's own...