| Search |
| [Next Page] |
Preparation of Ferrate solution.
[rquote=443036&tid=65699&author=ave369]A little question: what is the isopropyl flame for? F ... |
24-3-2016 at 05:07
by: moonfisher |
Preparation of Ferrate solution.
Forgot to add the reaction:
2 Fe(OH)3 + 3 OCl− + 4 OH− → 2 [FeO4]2− + 5 H2O + 3 Cl−
... |
23-3-2016 at 14:47
by: moonfisher |
Preparation of Ferrate solution.
Iron is almost always on the cationic part of the ionic substance. However, using strong oxidants, I ... |
23-3-2016 at 14:45
by: moonfisher |
Boxwood odor
Thanks again! More to read. |
20-3-2016 at 13:28
by: moonfisher |
Boxwood odor
[rquote=442328&tid=65586&author=CuReUS][rquote=442267&tid=65586&author=moonfisher]
... |
18-3-2016 at 03:18
by: moonfisher |
Boxwood odor
[rquote=442029&tid=65586&author=CuReUS][rquote=441976&tid=65586&author=moonfisher]
... |
17-3-2016 at 16:40
by: moonfisher |
Boxwood odor
CuReUS,
Don't worry! Ill do it! (eventually  )
Im planning to make the hydroxybutanone this wee ... |
15-3-2016 at 14:24
by: moonfisher |
Paper on cis-1,2 Cyclohexanediol
[rquote=441750&tid=65595&author=Dr.Bob]The first is a classic method, the second article I c ... |
14-3-2016 at 12:57
by: moonfisher |
Boxwood odor
[rquote=441801&tid=65586&author=CuReUS][rquote=441667&tid=65586&author=CuReUS]
4.co ... |
14-3-2016 at 12:51
by: moonfisher |
Boxwood odor
[rquote=441797&tid=65586&author=Bert][rquote=441725&tid=65586&author=Magpie][rquote= ... |
14-3-2016 at 12:46
by: moonfisher |
Paper on cis-1,2 Cyclohexanediol
First, this easy and seemingly OTC method:
http://pubs.acs.org/doi/abs/10.1021/jo01098a606
It's ev ... |
13-3-2016 at 15:42
by: moonfisher |
Boxwood odor
[rquote=441686&tid=65586&author=clearly_not_atara]From levulinic acid:
1. cycloenolizatio ... |
13-3-2016 at 15:34
by: moonfisher |
Boxwood odor
[rquote=441667&tid=65586&author=CuReUS][rquote=441623&tid=65586&author=moonfisher]
... |
13-3-2016 at 15:24
by: moonfisher |
Boxwood odor
[rquote=441628&tid=65586&author=Magpie]I like the smell of boxwood in the summer. When I se ... |
13-3-2016 at 15:19
by: moonfisher |
Boxwood odor
You know the smell of boxwood in the summer sun? Its an interesting odor. Turns out its made of 4-me ... |
12-3-2016 at 18:00
by: moonfisher |
Boron esters
Thanks for all the help, but it turns out my cyclohexanediol was even shittier than I thought. Might ... |
12-3-2016 at 17:46
by: moonfisher |
Copper and Ammonia
I second aga, it is a stunning blue, like the finest gentiana. Sometimes, copper (ii) boride looks a ... |
11-3-2016 at 16:19
by: moonfisher |
Boron esters
[rquote=441366&tid=65560&author=j_sum1]Cool question. Paging chemplayer.
I suspect the a ... |
11-3-2016 at 16:18
by: moonfisher |
Boron esters
Let's say you make an ester of boric acid and cis1-2Cyclohexanediol. How would the crystal structure ... |
10-3-2016 at 14:58
by: moonfisher |
Getting aq. solutions of inert metals without killing myself
J_sum,
Thanks for the link! I knew about the company, but I couldn't for the life of me remember ... |
26-2-2016 at 13:18
by: moonfisher |
Getting aq. solutions of inert metals without killing myself
[quote]
If that is the case, scrub the NOx through a solution of sodium hydroxide.
(Or recover i ... |
24-2-2016 at 15:07
by: moonfisher |
Getting aq. solutions of inert metals without killing myself
[quote]
Maybe electrolysis with a silver anode in acetic acid, sulfamic acid, or ammonia? Keep ... |
22-2-2016 at 15:07
by: moonfisher |
Copper(I) Iodide Synthesis
Yah, forgot to mention, used sodium sulfite + weak sulfamic acid. Thanks for reminding me! lol (the ... |
20-2-2016 at 14:31
by: moonfisher |
Getting aq. solutions of inert metals without killing myself
I want to try some neat silver chemistry, and I am going to get 2 nice 1g mini-rods of Ir metal.
... |
20-2-2016 at 13:08
by: moonfisher |
Copper(I) Iodide Synthesis
Thanks everyone! Worked like a charm (~95% yield on copp. acetate) about 10g of CuI. (Ill post the p ... |
20-2-2016 at 12:35
by: moonfisher |
| [Next Page] |
