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Reduction of levulinic acid
you could use Sn/HCl for reducing ketones to alcohols
[url]https://books.google.co.in/books?id=gKPt ... |
17-12-2014 at 02:14
by: CuReUS |
Tired of reporting spam
good topics are getting pushed down because of spam
they should make a system where you would ne ... |
16-12-2014 at 07:24
by: CuReUS |
Thioacetone
in the video ,he said thioacetone was a "thiol"
i think he meant "thione"
paddy ,why dont you tr ... |
16-12-2014 at 03:38
by: CuReUS |
Organic halides with piperdine
[rquote=378495&tid=54714&author=DJF90] However, in reality, the piperidine is (probably?) a ... |
16-12-2014 at 02:50
by: CuReUS |
xylene to benzene: HCl + al
[rquote=377870&tid=54648&author=blogfast25]
Neither are practical options for a beginner. O ... |
14-12-2014 at 03:47
by: CuReUS |
List some BAD chemistry YouTube videos
see this
[url]https://www.youtube.com/watch?v=bZ0PZWC17OA&src_vid=Gntz_fgCum0&feature=iv ... |
14-12-2014 at 02:55
by: CuReUS |
Vilsmeier-Haack Reaction
[rquote=377895&tid=53430&author=careysub]
Yes, Nicodem is - to use the French (not English) ... |
13-12-2014 at 20:40
by: CuReUS |
Vilsmeier-Haack Reaction
forget POCl[sub]3[/sub] or any other chemical
even nicodem (who always gives the best ideas) is ... |
13-12-2014 at 02:24
by: CuReUS |
Reduction of levulinic acid
[rquote=216361&tid=17051&author=Ninja]is raney nickel usable with formic acid (i doubt it... ... |
13-12-2014 at 01:58
by: CuReUS |
Bras ,batteries ,benzene and something in between
i dont require nickel anymore ,as nitinol is available so easily
i will follow the orsyn page for ... |
13-12-2014 at 01:53
by: CuReUS |
xylene to benzene: HCl + al
this would be a really bad method ,but if you really want benzene from xylene
why dont you oxidise ... |
13-12-2014 at 00:56
by: CuReUS |
Reduction of levulinic acid
[rquote=316927&tid=17051&author=Crowfjord]Ninja: Alkoxides are certainly terrible reducing a ... |
12-12-2014 at 01:33
by: CuReUS |
Preparation of 2,4-dinitrobromobenzene
[rquote=324553&tid=28480&author=PHILOU Zrealone]Won't 2,4-dinitrobromobenzene react with the ... |
11-12-2014 at 23:44
by: CuReUS |
Investigation of H2O2's decomposition while boiling
[rquote=318481&tid=28881&author=alexleyenda]
It's hard to prevent overflow when the boiling ... |
11-12-2014 at 05:26
by: CuReUS |
Is Raney Nickel inherently flamable, or only after pressure reactions?
[rquote=376307&tid=35812&author=FireLion3]Guys I am getting some Raney Nickel from a supplie ... |
10-12-2014 at 00:33
by: CuReUS |
An alternative to toxic 1,1-dimethylhydrazine (aka UDMH) as hypergolic rocket fuel
read this book ,you may find it useful
[url]http://library.sciencemadness.org/library/books/ignit ... |
9-12-2014 at 09:10
by: CuReUS |
Bras ,batteries ,benzene and something in between
[rquote=376006&tid=53527&author=phlogiston]
Nickel salts are used in electroplating soluti ... |
9-12-2014 at 08:44
by: CuReUS |
Vilsmeier-Haack Reaction
2nd page ,under "Reagents"
[url]http://www.ijpcbs.com/files/04-37.pdf[/url]
also read the third ... |
9-12-2014 at 08:10
by: CuReUS |
Vilsmeier-Haack Reaction
cobalt chloride may be substituted for POCl[sub]3[/sub]
if you want to make only aryl aldehydes ... |
9-12-2014 at 02:59
by: CuReUS |
p-hydroxybenzonitrile synthesis
instead of using CuCN ,one can also use copper powder in the presence of excess aqueous KCN
see ... |
9-12-2014 at 02:13
by: CuReUS |
Canned Air - Hydrofluoric Acid
[rquote=376170&tid=53719&author=BobD1001]
Quite scary however and in the future I will cert ... |
9-12-2014 at 01:07
by: CuReUS |
p-hydroxybenzonitrile synthesis
what about this route
nitrobenzene to Phenyl hydroxyl amine using Zn/aq NH[sub]4[/sub]Cl
[url] ... |
8-12-2014 at 02:48
by: CuReUS |
Bras ,batteries ,benzene and something in between
for quite sometime now ,many questions have been bothering me. They span across all fields ,from org ... |
8-12-2014 at 02:26
by: CuReUS |
Interesting source of tin
can't they just dip an aluminum piece in molten tin(like galvanizing) ,and then cut and beat it into ... |
7-12-2014 at 09:23
by: CuReUS |
Interesting source of tin
"tin" cans are actually aluminum cans with a thin layer of tin coating inside
so why can't the c ... |
7-12-2014 at 08:57
by: CuReUS |
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