Guest jaydee Posted April 9, 2004 Share Posted April 9, 2004 Hi, I was wondering what chemical test you could perform to identify an unsaturated compound. Thanks. Jaydee Link to comment Share on other sites More sharing options...
aommaster Posted April 9, 2004 Share Posted April 9, 2004 Bromine water. It goes colourless. e.g. Ethene Put bromine water with ethene and it forms 1,1 dibromoethene Link to comment Share on other sites More sharing options...
Guest jaydee Posted April 9, 2004 Share Posted April 9, 2004 So, putting bromine water with any unsaturated compound, (any alkene,alkyne etc) will result in making it go colourless? What I mean is, can this test for 'any' unsaturated compound, eg. if i mix say.. ethyne with bromine? Link to comment Share on other sites More sharing options...
aommaster Posted April 9, 2004 Share Posted April 9, 2004 yup! It works! Link to comment Share on other sites More sharing options...
Guest jaydee Posted April 9, 2004 Share Posted April 9, 2004 Ok thanks, very cool. Um, I know when a hydrocarbon is 'completely' combusted, it gives us CO2 and H2O, what if its 'incomplete', what does it give us? Link to comment Share on other sites More sharing options...
aommaster Posted April 9, 2004 Share Posted April 9, 2004 It gives CO2, H2O, C (carbon) and CO (carbon monoxide) Link to comment Share on other sites More sharing options...
budullewraagh Posted May 23, 2004 Share Posted May 23, 2004 a good way is to add a superacid like HF:SbF5 or HSO3-SbF5. it's hilarious; they can completely protonate alcohols and long chains of hydrocarbons. Link to comment Share on other sites More sharing options...
aommaster Posted May 23, 2004 Share Posted May 23, 2004 what do you mean by "protonate"? Link to comment Share on other sites More sharing options...
blike Posted May 23, 2004 Share Posted May 23, 2004 aommaster, in organic chemistry when you say "protonate" it means to throw on a proton (hydrogen atom). If you protonate an alcohol, you go from R- OH to R- OH2+ Link to comment Share on other sites More sharing options...
aommaster Posted May 23, 2004 Share Posted May 23, 2004 oh ok! Thanx alot Blike! Link to comment Share on other sites More sharing options...
budullewraagh Posted May 23, 2004 Share Posted May 23, 2004 yeah, what's really disturbing is that a 50% solution of HF:SbF5 is 10^18x as acidic as conc H2SO4. if you drop a candle into it, the candle will cease to exist quite quickly. if you stick a hand in it, your hand will cease to exist quite quickly. the most acidic substance i've ever worked with is a saturated solution of HCl, and that dissolved a small piece of styrofoam within seconds. imagine conc HF:SbF5 Link to comment Share on other sites More sharing options...
aommaster Posted May 24, 2004 Share Posted May 24, 2004 LOL! I read that in the guiness book of records! Antimony Pentafluoride must be a really scary substance! What do they store it in? Link to comment Share on other sites More sharing options...
budullewraagh Posted May 25, 2004 Share Posted May 25, 2004 Antimony Pentafluoride must be a really scary substance! ^ only when mixed with a substance that ionizes to yield H+. i'm not sure what it's stored in, but i could imagine it would be some pretty strong glass. Link to comment Share on other sites More sharing options...
aommaster Posted May 26, 2004 Share Posted May 26, 2004 I heard that it does not eat through specific plastics or something. I think that is what they store it in. Not sure though! Link to comment Share on other sites More sharing options...
YT2095 Posted May 26, 2004 Share Posted May 26, 2004 HAZARDOUS DECOMPOSITION PRODUCTS: Decomposes into antimony and hydrofluoric acid with heating or water contact. Decomposition products reactwith glass. taken from: http://66.102.9.104/search?q=cache:8jb8Z_THpQkJ:www.boc.com/gases/pdf/msds/G121.pdf+%22Antimony+Pentafluoride%22&hl=en Link to comment Share on other sites More sharing options...
aommaster Posted May 26, 2004 Share Posted May 26, 2004 ummmm... does that answer my question? If it does, could you please explain further? Link to comment Share on other sites More sharing options...
YT2095 Posted May 26, 2004 Share Posted May 26, 2004 sure, it can be stored in any plastic or metal (it mentioned weldable metal drums) that won`t react with Flourine Link to comment Share on other sites More sharing options...
aommaster Posted May 26, 2004 Share Posted May 26, 2004 What metal wouldn't react with fluroine? And which plastic? Link to comment Share on other sites More sharing options...
YT2095 Posted May 26, 2004 Share Posted May 26, 2004 I`m fairly sure polyprop plastic doesn`t, as for the metals I`m not sure off the top of my head, but it`ll be something quite ordinary, just as Nitric Acid can and is safely stored in Aluminium containers Link to comment Share on other sites More sharing options...
aommaster Posted May 26, 2004 Share Posted May 26, 2004 hmmmm.... would aluminium oxide reacti with fluorine? I don't think so because it is unreactive. This leads me to think that aluminium containers would be good to store the acid! Link to comment Share on other sites More sharing options...
YT2095 Posted May 26, 2004 Share Posted May 26, 2004 Antimony Pentafluoride attacks glass copper and lead, but other than that, if it`s kept perfectly dry, it`s quite safe take a peek here too :http://www.inchem.org/documents/icsc/icsc/eics0220.htm Link to comment Share on other sites More sharing options...
aommaster Posted May 26, 2004 Share Posted May 26, 2004 Thanx YT. Great link! Link to comment Share on other sites More sharing options...
RachRox Posted March 2, 2006 Share Posted March 2, 2006 Hi! was just wondering about the unsaturates test with bromine water. what is the name of the chemical reaction that has taken place here?? xx:confused: Link to comment Share on other sites More sharing options...
budullewraagh Posted March 2, 2006 Share Posted March 2, 2006 the reaction is an anti addition. the electrons from the pi bond of the ethene attack one atom of bromine in the diatomic molecule, causing the electrons from the sigma bond between Br and Br to go to the Br atom that was not attacked by the pi bond. simultaneously, the Br attacked by the pi bond puts a lone pair of electrons on the other carbon, making it bonded to two carbon atoms and positively charged. finally, the bromide anion performs an sN2 reaction, attacking one carbon, inverting the stereochemistry and causing the electrons from the C-Br+ bond to go to the bromine atom. Step 1: Br-Br H2C=CH2 Step 2: Br- H2C(Br+)CH2 Step 3: H2BrC-CBrH2 Link to comment Share on other sites More sharing options...
insane_alien Posted March 2, 2006 Share Posted March 2, 2006 addition Link to comment Share on other sites More sharing options...
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