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Synthesis of longer chain tertiary alcohols @Nicodem: Thanks. The de-esterification of terpineol acetate won't be easy either though, I imagi ...	12-1-2016 at 09:51 by: blogfast25
Hydrochlorination of alk-1-ene? [rquote=434983&tid=64979&author=Nicodem] Yes, it qualifies very well for an electrophilic a ...	12-1-2016 at 09:38 by: blogfast25
Using a small deep fryer as an oil bath I use one too. No problems at all.	12-1-2016 at 07:47 by: blogfast25
Synthesis of longer chain tertiary alcohols [rquote=434962&tid=15171&author=aga]OK. So i need to have a good long stare at dissolution i ...	12-1-2016 at 07:02 by: blogfast25
Hydrochlorination of alk-1-ene? [rquote=434921&tid=64979&author=byko3y]I've had such experience. I've used silica gel as a c ...	11-1-2016 at 15:38 by: blogfast25
Synthesis of longer chain tertiary alcohols [rquote=434919&tid=15171&author=aga] [b]I.[/b] If they Dissolve and not simply Mix, Acetone ...	11-1-2016 at 15:24 by: blogfast25
RogueSci Ok, maybe we should drop this NBK stuff now? I mean, what next on SM, snuff movies?	11-1-2016 at 14:50 by: blogfast25
Equilibrium constant question [rquote=434897&tid=64986&author=SunriseSunset]Does anyone know a youtube video that shows th ...	11-1-2016 at 14:45 by: blogfast25
Synthesis of longer chain tertiary alcohols Take HCl as a simpler example (monoprotic). As a strong acid it completely deprotonates: HCl(aq) ...	11-1-2016 at 14:27 by: blogfast25
Synthesis of longer chain tertiary alcohols double post eliminated [Edited on 11-1-2016 by blogfast25]	11-1-2016 at 14:06 by: blogfast25
Hydrochlorination of alk-1-ene? [rquote=434901&tid=64979&author=Nicodem]The [i]Organic Syntheses[/i] example is a Michael ad ...	11-1-2016 at 13:34 by: blogfast25
Synthesis of longer chain tertiary alcohols [rquote=434896&tid=15171&author=aga] [b]I.[/b] The system isn't really uniphasic - if left ...	11-1-2016 at 12:57 by: blogfast25
Notes on acetone as a solvent (here) The need for a solvent has already been explained in terms of homogeneous catalysis being generally ...	11-1-2016 at 09:25 by: blogfast25
RogueSci The real danger though is terrorism. The chemistry of these things has been known for a long time, I ...	11-1-2016 at 08:25 by: blogfast25
Making copper salts (especially basic copper carbonate) [rquote=434091&tid=64890&author=Fulmen] Edit: This process is also said to produce a unif ...	11-1-2016 at 03:45 by: blogfast25
RogueSci [rquote=434871&tid=63069&author=woelen]I can imagine that these people really try to do thes ...	11-1-2016 at 03:22 by: blogfast25
Make Potassium (from versuchschemie.de) [rquote=434858&tid=14970&author=NeonPulse]I had today only received my 99.9% ingots of Mg to ...	11-1-2016 at 03:19 by: blogfast25
Equilibrium constant question [rquote=434868&tid=64986&author=SunriseSunset]So my book has an equilibrium constant of = 1. ...	11-1-2016 at 02:43 by: blogfast25
Make Potassium (from versuchschemie.de) [rquote=434832&tid=14970&author=Etaoin Shrdlu]That one looks nice too.[/rquote] I'm afrai ...	10-1-2016 at 18:33 by: blogfast25
Hydrochlorination of alk-1-ene? [rquote=434834&tid=64979&author=Magpie]I heated a mixture of 95% NaHSO4 and NaCl. The mix w ...	10-1-2016 at 18:04 by: blogfast25
Synthesis of longer chain tertiary alcohols The more I look at that paper (TCA, 2013) the less I like it. There are real ABSURDITIES in it. ...	10-1-2016 at 17:42 by: blogfast25
Make Potassium (from versuchschemie.de) [rquote=434828&tid=14970&author=Etaoin Shrdlu]Ran across this while cleaning and thought som ...	10-1-2016 at 17:09 by: blogfast25
Synthesis of longer chain tertiary alcohols The abstract of that paper: [quote]Chloroacetic acid was used as catalyst for the hydration of α ...	10-1-2016 at 16:29 by: blogfast25
Synthesis of longer chain tertiary alcohols [rquote=434822&tid=15171&author=aga] TCA as catalyst producing more alpha-terpineol in less ...	10-1-2016 at 15:50 by: blogfast25
Hydrochlorination of alk-1-ene? [rquote=434820&tid=64979&author=Magpie]You may find this useful: http://www.sciencemadnes ...	10-1-2016 at 15:31 by: blogfast25
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