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The reaction of chlorosulfonic acid with different metals
What about using ice cubes for disposal of small quantities? |
24-9-2021 at 07:26
by: njl |
Secret Santa 2021
Same boat Herr, I never heard from if my pack was received. |
21-9-2021 at 07:17
by: njl |
5-hydroxyvanillin methylation?
Vanillin will undergo a Cannizarro reaction with base. |
8-9-2021 at 07:43
by: njl |
Synthesis of Boron Trichloride?
A steel vessel might survive a few runs at most if you want to chlorinate simultaneously. It is very ... |
20-8-2021 at 09:46
by: njl |
Lithium hydride crystalline, 98% FOR SALE
They will more or less participate in the same reactions as bases, but I think Li being a smaller at ... |
20-8-2021 at 08:34
by: njl |
Synthesis of Boron Trichloride?
It's definitely doable, just not a great source. Takes a good amount of effort to get a commodity ch ... |
20-8-2021 at 08:30
by: njl |
Synthesis of Boron Trichloride?
So it's really just a carbothermal reduction of borax to boron, the boron then leaves the reaction a ... |
20-8-2021 at 05:19
by: njl |
Metal picolinates
I think the carboxylate being adjacent to the amine's lone pair allows for different complexes to fo ... |
2-8-2021 at 04:02
by: njl |
Protecting groups for tertiary amines
[url=https://sci-hub.st/10.1016/j.cclet.2018.01.003]Acetic acid catalyzed ester aminolysis[/url]
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31-7-2021 at 11:14
by: njl |
Making Sodium, a new method?
excellent point ark |
28-7-2021 at 04:53
by: njl |
Protecting groups for tertiary amines
[rquote=663094&tid=157678&author=Monoamine][rquote=662526&tid=157678&author=karlos³ ... |
21-7-2021 at 05:11
by: njl |
Protecting groups for tertiary amines
I think the phenolate will react much more quickly compared to the amine. |
17-7-2021 at 07:02
by: njl |
Protecting groups for tertiary amines
Or deprotonate and perform William ether synthesis |
17-7-2021 at 06:32
by: njl |
Means of titrating calcium cyanamide
I think measuring the amount of ammonia given off during hydrolysis is your best bet. Hydrolyze a kn ... |
4-7-2021 at 05:31
by: njl |
Preparation of NaH from sodium metal.
No, elimination of a beta hydrogen + electron from an alkoxide would give a carbonyl and hydride, el ... |
30-6-2021 at 12:55
by: njl |
Preparation of NaH from sodium metal.
Might the same concept apply to more easily obtained alkoxides? Equivalent beta elimination would gi ... |
30-6-2021 at 04:49
by: njl |
foaming Borax!
Maybe forming NaHCO3 and boric acid? |
28-6-2021 at 02:35
by: njl |
How do reactions at electrodes proceed: Peroxidation vs. Esterification vs. unknown synthesis.
The answers to many of these questions may be found in the chemistry of radicals. Reading up on radi ... |
25-6-2021 at 16:59
by: njl |
Chemicals & Glassware for Sale - Price Drop
HAD to snatch up that NaBH4 and NaBF4. Arrived as 2 bottles of NaBF4 and some bags of NaBH4. The ind ... |
25-6-2021 at 16:35
by: njl |
Thionly chloride from batteries
I've looked into it a little, they seem very expensive for a frankly tiny amount of SOCl2 |
25-6-2021 at 16:27
by: njl |
Preparation of NaH from sodium metal.
I was more familiar with sodium hydride's deprotonation of the 3 position on indoles. What is it str ... |
24-6-2021 at 13:09
by: njl |
Is there anything interesting I can do with Urea?
[rquote=661835&tid=157609&author=S.C. Wack]
Indirectly, urea has been used to decarboxylate ... |
20-6-2021 at 08:29
by: njl |
What does "drying over" some desiccant mean?
It is also (perhaps incorrectly) used to mean drying a product in a sealed vessel containing the dry ... |
19-6-2021 at 17:08
by: njl |
Is diphosphorus pentoxide hygroscopic?
Yeah |
19-6-2021 at 06:39
by: njl |
Latest chemical order?
This is probably not the right place for it but I thought I'd mention I saw moth killer at the hardw ... |
17-6-2021 at 06:44
by: njl |
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