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Beginer benzene synthesis (No hydroxide)
CaO +C[sub]6[/sub]H[sub]5[/sub]CO[sub]2[/sub]H -> CaCO[sub]3[/sub] +C[sub]6[/sub]H[sub]6[/sub], b ... |
10-2-2014 at 19:47
by: DraconicAcid |
Pseudoscience & Willful Ignorance
[rquote=318375&tid=27407&author=Etaoin Shrdlu][url=http://www.highexistence.com/water-experi ... |
8-2-2014 at 12:46
by: DraconicAcid |
Copper(II) Aspirinate Synthesis
I suspect your structure for copper(II) benzoate is inaccurate. Isn't it similar to the acetate, ac ... |
6-2-2014 at 21:06
by: DraconicAcid |
Copper(II) Aspirinate Synthesis
Nice video, but it's incorrect to refer to the copper aspirinate as a ligand. The aspirinate ion ac ... |
4-2-2014 at 15:25
by: DraconicAcid |
Successful experiments
I made cis-bis(glycinato)copper(II) the other day. The reactants combined to give a glorious dark p ... |
4-2-2014 at 10:37
by: DraconicAcid |
Removal of gasses
[rquote=317888&tid=28821&author=Brain&Force]Wouldn't this produce aqua regia, and theref ... |
4-2-2014 at 10:34
by: DraconicAcid |
Removal of gasses
[rquote=317887&tid=28821&author=Zyklonb]DraconicAcid, " I think you'd better read something ... |
4-2-2014 at 10:31
by: DraconicAcid |
Removal of gasses
[rquote=317880&tid=28821&author=Zyklonb]According to Wikipedia, NaOCl(aq), has an Acidity (p ... |
4-2-2014 at 09:56
by: DraconicAcid |
Removal of gasses
[rquote=317850&tid=28821&author=woelen]Mixes of NO and NO2 are harder to scrub. NO does not ... |
4-2-2014 at 09:35
by: DraconicAcid |
Organometallic Chemistry
[quote]Aside from a metal atom, the other stuff is mainly organic.[/quote]
That's a bit like sayi ... |
3-2-2014 at 13:54
by: DraconicAcid |
Organometallic Chemistry
[rquote=317706&tid=28801&author=TheChemiKid]Even simpler, there are some simple organometall ... |
3-2-2014 at 08:29
by: DraconicAcid |
Organometallic Chemistry
[rquote=317641&tid=28801&author=Random]Organometallic chemistry often requires dangerous rea ... |
2-2-2014 at 14:40
by: DraconicAcid |
how to precipitate ferrous oxalate in solution
[rquote=317582&tid=28782&author=blogfast25]
But Mn<sup>2+</sup> pink colour is ... |
2-2-2014 at 12:18
by: DraconicAcid |
how to precipitate ferrous oxalate in solution
Pink? Might there be a manganese impurity in your iron oxide? |
31-1-2014 at 22:30
by: DraconicAcid |
Published a paper on a previous work :)
Well done! |
31-1-2014 at 12:02
by: DraconicAcid |
Little things that surprised you in chemistry
[rquote=317307&tid=28474&author=Brain&Force]Ferric nitrate is so weird. It starts off as ... |
30-1-2014 at 20:44
by: DraconicAcid |
Making Copper Acetate?
[rquote=316650&tid=11144&author=mr.crow]Just a note that vinegar is not suitable for chemist ... |
30-1-2014 at 17:51
by: DraconicAcid |
Noob Solution Percentage Question
The 10% is almost certainly by mass (although some chemists would use mass/volume percent, which is ... |
30-1-2014 at 16:11
by: DraconicAcid |
Arecoline extraction
Arecoline is an ester- a strong base like sodium hydroxide could hydrolyze it to the sodium salt of ... |
30-1-2014 at 09:43
by: DraconicAcid |
Winter sun looks dark
[rquote=317139&tid=28753&author=maxpayne]Yeah, I was waiting for you guys. The high-priests ... |
29-1-2014 at 16:38
by: DraconicAcid |
Nicotine extraction
I would be surprised if an amine like nicotine didn't coordinate to copper(I) or copper(II). |
29-1-2014 at 13:13
by: DraconicAcid |
Nicotine extraction
That should work. The nicotine is very water soluble, though, so it won't precipitate from the solu ... |
29-1-2014 at 12:43
by: DraconicAcid |
Nicotine extraction
Once you get nicotine hydrochloride, you can react it with a base to give the free amine. |
29-1-2014 at 12:34
by: DraconicAcid |
Got Pyridine?
[rquote=317076&tid=28749&author=SM2]I'm not naming names, but a parcel of this left on my po ... |
29-1-2014 at 10:19
by: DraconicAcid |
Propane burner smell
Yes, it would also burn.
The only time I've smelled unburned gas when using a propane torch, it w ... |
27-1-2014 at 13:31
by: DraconicAcid |
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