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Acetic anhydride preparation
I think you're more likely to just get a mess of aldol condensation products.  |
11-2-2011 at 18:16
by: madscientist |
LED Dangers - Unbelievable Paranoia!
Children mistaking light bulbs for candy is a stretch. Also seems silly to don a moonsuit before swe ... |
11-2-2011 at 13:47
by: madscientist |
make dry hex-1-yne
I think he means drying hex-1-yne with molecular sieves 4A. |
10-2-2011 at 21:45
by: madscientist |
make dry hex-1-yne
I assume you meant CaC<sub>2</sub>. What are the other reagents and conditions? |
10-2-2011 at 14:19
by: madscientist |
L-tryptophan decarboxylation
That's actually the same paper I was going to post!  |
8-2-2011 at 14:30
by: madscientist |
L-tryptophan decarboxylation
Conditions don't have to be what we'd consider acidic in order for it to occur. I have a paper on th ... |
8-2-2011 at 13:15
by: madscientist |
L-tryptophan decarboxylation
The use of a ketone catalyst will result in the formation of beta-carbolines (Pictet-Spengler), whic ... |
8-2-2011 at 11:57
by: madscientist |
Oxidation of Ethanol to Ethanal?
No, it doesn't. |
7-2-2011 at 21:07
by: madscientist |
Oxidation of Ethanol to Ethanal?
Yes. |
7-2-2011 at 20:57
by: madscientist |
Oxidation of Ethanol to Ethanal?
Is this the first time you looked at any of the material for your class?
You already were given t ... |
7-2-2011 at 20:36
by: madscientist |
Oxidation of Ethanol to Ethanal?
That is the mechanism! |
7-2-2011 at 20:18
by: madscientist |
Is my NaBH4 legit?
Perhaps by addition of KMnO<sub>4</sub> to a cold, strongly alkaline solution of NaBH< ... |
5-2-2011 at 13:05
by: madscientist |
Fries Rearrangement and Sulphonation
I think he just overestimated our knowledge! 
Low temperature products are kinetic products (lo ... |
5-2-2011 at 11:00
by: madscientist |
RE: Lost Discussion (Sabot Light AP Round)
Chemistry is a science, and our experiments are madness.
Weapons discussion has not been tolerate ... |
5-2-2011 at 02:05
by: madscientist |
Is my NaBH4 legit?
NaBH<sub>4</sub> doesn't decompose too quickly in neutral aqueous solution. It does in d ... |
4-2-2011 at 18:14
by: madscientist |
Extraction of Mn2O7 using CCl4?
I owe you an apology, my writing was unclear - I was referring to others in the thread. Sorry about ... |
4-2-2011 at 18:08
by: madscientist |
Extraction of Mn2O7 using CCl4?
I can't read German so I'm unable to comment on that.
The reference I gave mentions the reaction ... |
4-2-2011 at 12:08
by: madscientist |
RE: Lost Discussion (Sabot Light AP Round)
By that reasoning, computer programming could be argued to be related to chemistry, as a lot of chem ... |
3-2-2011 at 20:24
by: madscientist |
RE: Lost Discussion (Sabot Light AP Round)
The utilization of heavy weapons has nothing to do with chemistry. |
3-2-2011 at 13:17
by: madscientist |
Extraction of Mn2O7 using CCl4?
It's good to offer warnings, but your current tone needs to go - you're derailing the thread.
Don ... |
3-2-2011 at 12:02
by: madscientist |
KMnO4 + HNO3
Oops... yes. Sorry. |
3-2-2011 at 05:03
by: madscientist |
KMnO4 + HNO3
If the evolved gasses are transparent, I would imagine you have potassium nitrate, manganese nitrate ... |
3-2-2011 at 04:28
by: madscientist |
Diethyl Ether from Denatured Alcohol
https://www.sciencemadness.org/whisper/viewthread.php?tid=9747 |
2-2-2011 at 18:19
by: madscientist |
RE: Lost Discussion (Sabot Light AP Round)
I don't like weapons discussion here. But some has to be tolerated in the interest of maintaining an ... |
2-2-2011 at 18:15
by: madscientist |
Site Protocals
If they've articulated any sort of desire for what you have, then it's fine by me. You might want to ... |
31-1-2011 at 07:07
by: madscientist |
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