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Safety Tips for n00bs/kw3ls
And gloves are not essential! I rather don't have them on with acids like HCl or other mild corrosiv ... |
25-5-2011 at 04:22
by: Jor |
SOCl2 via COCl2
Sedit, the formation of SOCl2 is an entirely different kind of reaction than formation of SO2Cl2. Th ... |
24-5-2011 at 10:01
by: Jor |
SOCl2 via COCl2
The text below is what I posted in another topic, but maybe it's better to give it it's own topic.
... |
24-5-2011 at 00:21
by: Jor |
Iodoform
Now that I think of it, I read on wikipedia that phosgene reacts with sulfur dioxide to form thionyl ... |
23-5-2011 at 16:15
by: Jor |
Iodoform
''One of quickest easiest ways of producing phosgene is with
carbon tetrachloride and hot metal. In ... |
23-5-2011 at 15:33
by: Jor |
Iodoform
Yes sorry, my mistake. I guess I read it too fast and skipped over the chloroform part  |
23-5-2011 at 10:14
by: Jor |
Iodoform
You mean as a byproduct of the reaction? If you filtered and dried it properly, it should be free of ... |
23-5-2011 at 08:40
by: Jor |
Acquiring Tert-amyl alcohol
To make ethylmagnesium bromide, all you need is KBr or NaBr, H2SO4 and ethanol to make bromoethane, ... |
23-5-2011 at 07:10
by: Jor |
Iodoform
Please tell me how you get phosgene by heating iodoform  |
23-5-2011 at 07:07
by: Jor |
school chemistry demo out-of-control
Yes I have seen this movie this before.
This teacher is obviously either very stupid or wasn't payi ... |
22-5-2011 at 07:24
by: Jor |
Anhydrous ions
No that's impossible. You can't just precitipate all but sodium-ions or any other ion. There will al ... |
21-5-2011 at 14:47
by: Jor |
rxn of P4 with Na in benzene
I did the experiment today. To a 50mL roundbottom flask was added a stirbar followed by 5mL of benze ... |
21-5-2011 at 13:55
by: Jor |
Reactions of disulfides to aid in their removal
Can't you reduce the disulfide bond to the thiol?
http://en.wikipedia.org/wiki/2-Mercaptoethanol
... |
20-5-2011 at 02:42
by: Jor |
Practice distillation of acetone.
I would imagine chloroform being able to attack PVC! But I'm not sure. |
16-5-2011 at 12:40
by: Jor |
Concerning the synthesis of Ethyl Acetate
I would use sodium bicarbonate instead of carbonate. When you add a little too much you wont have to ... |
15-5-2011 at 09:03
by: Jor |
Concerning the synthesis of Ethyl Acetate
You need to use H2SO4 as a catalyst or it will take forever for the equillibrium to set in. Look up ... |
15-5-2011 at 07:50
by: Jor |
HgCl2
You can make the HgCl2 yourself though, from elemental mercury. However this is dangerous.
I do not ... |
14-5-2011 at 08:21
by: Jor |
rxn of P4 with Na in benzene
Until i can start with my project on ibuprofen (I think a few more weeks) I am doing some random exp ... |
14-5-2011 at 07:24
by: Jor |
Indium compounds
Can you dilute the indium nitrate solution. I think it will turn clear. or boil it.
When you disso ... |
12-5-2011 at 06:53
by: Jor |
Looking to buy 10L of Benzene!
Try toluene or some other solvent. 10L of benzene is not nothing! |
10-5-2011 at 11:24
by: Jor |
Bad days in the lab or with glassware?
I hardly every break glassware. In my 4 years of amateur chemistry, I broke 1 erlenmeyer, about 4 be ... |
8-5-2011 at 14:56
by: Jor |
Fluorine gas non-electrical production
''Gaseous HF is so poisonous because undissociated HF molecules are readily soluble in fatty tissue. ... |
8-5-2011 at 05:52
by: Jor |
Fluorine gas non-electrical production
[rquote=209181&tid=16246&author=blogfast25]Jor and Anders:
Ok. Keep relativating the dang ... |
7-5-2011 at 14:25
by: Jor |
Fluorine gas non-electrical production
[rquote=208971&tid=16246&author=blogfast25]This guy Publios (from the video) is a nutcase: t ... |
6-5-2011 at 18:01
by: Jor |
Fluorine gas non-electrical production
[rquote=208942&tid=16246&author=plante1999]You are very crazy , dont make F2 it will kill yo ... |
4-5-2011 at 15:50
by: Jor |
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