| Search |
| [Next Page] |
wall wart as power supply for electrolysis
While this isn't good practice I have to admit I've used them before, they will work for some reacti ... |
11-5-2021 at 05:04
by: njl |
Aldehyde oxidation
Any tips for making concentrated Ca(OCl)2 solutions? |
10-5-2021 at 16:03
by: njl |
Aldehyde oxidation
I was avoiding acetone because it reacts violently with hypochlorite. I think isopropanol should hol ... |
10-5-2021 at 10:56
by: njl |
Aldehyde oxidation
I am going to try the reaction outlined in [url=https://sci-hub.st/https://doi.org/10.1016/S0040-403 ... |
10-5-2021 at 10:12
by: njl |
What is this metal?
[rquote=659559&tid=157392&author=vano][rquote=659557&tid=157392&author=njl]Make a fu ... |
7-5-2021 at 06:42
by: njl |
What is this metal?
Make a fusion weapon |
7-5-2021 at 05:25
by: njl |
Question about Ethyl Bromide
If you manage to make bromophosgene in this scenario you're either trying to make bromophosgene or s ... |
5-5-2021 at 07:21
by: njl |
Report on making metal sorbates
[quote]
The filtrate and wash water run through was red meaning either the cobalt sulphate was in e ... |
5-5-2021 at 00:15
by: njl |
The Short Questions Thread (4)
Carbon monoxide is a better reducing agent than it is an oxidizing agent, and ammonia needs to be ox ... |
4-5-2021 at 16:30
by: njl |
Acetic anhydride preparation
I think it works via addition of HCl to the nitrile to form an imidoyl chloride, this reacts with Ac ... |
4-5-2021 at 08:23
by: njl |
Acetic anhydride preparation
Well half of the acetonitrile is consumed as acetamide HCl. The advantage to this reaction isn't yie ... |
4-5-2021 at 05:39
by: njl |
Nomenclature of Coordinative Compounds
For some reason I always see Cp first as in (Cp)2[TiCl2]. Whether or not that's correct, I don't kno ... |
4-5-2021 at 05:32
by: njl |
Hg salts for sale
[rquote=659303&tid=157382&author=Chemcraft]Thank you.
By the end of May, we plan to start ... |
4-5-2021 at 05:30
by: njl |
Report on making metal sorbates
Could the density then be increased by finely powdering the product? |
4-5-2021 at 04:47
by: njl |
Ketalization of Phenol
Ok, so you want something like intermediate 5 from scheme 1?
[quote]
Methyl ortho-Bromo-Benzoat ... |
4-5-2021 at 04:45
by: njl |
3 NaClO → 2 NaCl + NaClO3 > KCl + NaClO3 → NaCl + KClO3
How fast can you make the reaction with Cl2 gas? Cl2 might be trivial to make for most of us, but ma ... |
3-5-2021 at 16:23
by: njl |
Hydroiodic acid from Vitamin C !
Yes and yes, but at least at room temperature the equilibrium would be towards HI. |
3-5-2021 at 14:02
by: njl |
Medicinal Compounds of Natural Origin
I think you and symboom would get along nicely. [url=http://www.sciencemadness.org/talk/viewthread.p ... |
3-5-2021 at 10:23
by: njl |
how to replicate this?
Well you asked how it's made, and that's how it's made (at least in that video). If you can't get dr ... |
3-5-2021 at 07:55
by: njl |
Report on making metal sorbates
The low density is an interesting effect. Have you tested the solubility? Maybe a crystallization wi ... |
3-5-2021 at 04:54
by: njl |
Acetic anhydride preparation
Yes it is, but experiments done by users on another forum showed that Chemplayer didn't use nearly e ... |
3-5-2021 at 04:52
by: njl |
Hydroiodic acid from Vitamin C !
Side products as well as unreacted starting materials. The ascorbic acid method is probably worse in ... |
2-5-2021 at 17:43
by: njl |
Acetic anhydride preparation
Keras, if you are going to try that would you perhaps also try the MeCN/HCl reaction for generating ... |
2-5-2021 at 14:41
by: njl |
Ammonium Acetate, what went wrong
Ammonium acetate is notoriously difficult to dry (deliquescent even) and I expect you will have to c ... |
1-5-2021 at 16:26
by: njl |
Hydroiodic acid from Vitamin C !
HI is probably formed since ascorbic acid is a reasonably good reducing agent but I don't think this ... |
1-5-2021 at 14:44
by: njl |
| [Next Page] |
