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Why are there two ways to express Acetate?
@DraconicAcid
[quote]Yes, I've seen it used in several textbooks. It's just wrong. The two oxygen ... |
3-9-2016 at 08:26
by: Alice |
The Short Questions Thread (4)
Thanks for the answer! No, nothing happend. I'm asking beforehand. I knew Mg powder is pyrophoric, t ... |
3-9-2016 at 02:38
by: Alice |
The Short Questions Thread (4)
Is there a possibility for a mixture of sodium hydroxide and magnesium metal, both powdered, to igni ... |
2-9-2016 at 10:37
by: Alice |
Synthesis of longer chain tertiary alcohols
@CuReUS.
Comptes rendus hebdomadaires des séances de l'Académie des Sciences:
http://gallic ... |
2-9-2016 at 00:11
by: Alice |
Synthesis of longer chain tertiary alcohols
[quote]Having said all that I'm now inclined to 'cut out the middleman' and purchase the alpha-terpi ... |
31-8-2016 at 08:40
by: Alice |
Synthesis of longer chain tertiary alcohols
[quote]Nah. Get it from eBay, Amazon or prepare it yourself. Not hard at all.[/quote]
@blogfast, ... |
31-8-2016 at 03:43
by: Alice |
Synthesis of longer chain tertiary alcohols
@CuReUS
If double hydration on limonene would work, it would work on terpineol as well, right?
... |
31-8-2016 at 00:43
by: Alice |
Synthesis of longer chain tertiary alcohols
Oxalic acid is available in hardware stores for rust removal and as optical brightener for wood.
... |
30-8-2016 at 14:42
by: Alice |
Green Synthesis of 3-methyl-heptan-3-ol from common materials
Twelve principles of Green Chemistry:
1. It is better to prevent waste than to treat or clean ... |
30-8-2016 at 14:19
by: Alice |
Synthesis of longer chain tertiary alcohols
Aga, can you remember how you achieved crystallization?
Considering the reported tiny amount of ... |
30-8-2016 at 03:23
by: Alice |
Synthesis of longer chain tertiary alcohols
I had a look at a paper mentioned previously:
"Synthesis of terpineol from α-pinene by homogeneo ... |
28-8-2016 at 17:28
by: Alice |
Ligands derived from niacin?
Oxidation of picoline by KMnO4:
http://orgsyn.org/demo.aspx?prep=CV3P0740
Oxidation of picolin ... |
28-8-2016 at 05:34
by: Alice |
Synthesis of longer chain tertiary alcohols
After reduction of the double bond a possible substitute for tBuOH is obtained, which is sterically ... |
26-8-2016 at 07:07
by: Alice |
Synthesis of longer chain tertiary alcohols
Unfortunately Kremer sells CAS 8000-41-7 which is an undefined mixture of terpineol isomers. Only a ... |
26-8-2016 at 06:31
by: Alice |
possibility for THC extraction
LOL |
25-8-2016 at 10:37
by: Alice |
possibility for THC extraction
What's so special about my name? Are we in kindergarten? |
25-8-2016 at 09:49
by: Alice |
Synthesis of longer chain tertiary alcohols
Possibly, yes. Nevertheless I would be more concerned about the double bond of alpha-pinene to be le ... |
25-8-2016 at 09:38
by: Alice |
Synthesis of longer chain tertiary alcohols
Of course alpha-pinene is the most abundant, interestingly the error is only found in the abstract o ... |
25-8-2016 at 07:20
by: Alice |
Synthesis of longer chain tertiary alcohols
"With aga now in self-imposed exile there won't be any, anytime soon I think."
This reminds me of ... |
25-8-2016 at 06:09
by: Alice |
possibility for THC extraction
I don't know anything about extraction, but regarding decarboxylation the following might be interes ... |
25-8-2016 at 05:53
by: Alice |
Synthesis of longer chain tertiary alcohols
[rquote=405156&tid=15171&author=blogfast25]That's very interesting Alice, thanks for your th ... |
16-5-2015 at 11:36
by: Alice |
Synthesis of longer chain tertiary alcohols
Here are the literature yields for the camphor derived alcohols:
2-methyl-: 64 %
2-ethyl-: 29 % ... |
16-5-2015 at 09:45
by: Alice |
Synthesis of longer chain tertiary alcohols
[rquote=404850&tid=15171&author=blogfast25]
No, no success has been reported so far.
Abo ... |
13-5-2015 at 16:23
by: Alice |
Synthesis of longer chain tertiary alcohols
So did anybody have success in manufacturing higher tertiary alcohols and use in making potassium?
... |
13-5-2015 at 15:00
by: Alice |
Batteries
Eventually by adding an alkali hydroxide to an aqueous solution. Fe hydroxides will precipitate. LiO ... |
13-5-2015 at 10:18
by: Alice |
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