skwiff Posted May 11, 2011 Posted May 11, 2011 is there a way to make iodine with out using acids and peroxides? I was thinking mixing solutions of KCl/NaCl and KI/NaI would this work? not sure on the ratios but in theory should work...
elementcollector1 Posted July 9, 2011 Posted July 9, 2011 I have no idea if that would work... Is there any particular reason you want to avoid peroxides and acids?
skwiff Posted July 13, 2011 Author Posted July 13, 2011 (edited) i can not obtain the acids or peroxides easily Edited July 13, 2011 by skwiff
elementcollector1 Posted July 24, 2011 Posted July 24, 2011 (edited) i can not obtain the acids or peroxides easily Sure ya can! Hydrochloric acid can be obtained at hardware stores like McLendon's for about $3-4, and hydrogen peroxide can be found at every pharmacy for half that. It really depends on what age you are, though. People will question you if you're young and buying this stuff. But if you are young, and really interested in making iodine, get your parents to buy this stuff for you. Edited July 24, 2011 by elementcollector1
skwiff Posted July 24, 2011 Author Posted July 24, 2011 Sure ya can! Hydrochloric acid can be obtained at hardware stores like McLendon's for about $3-4, and hydrogen peroxide can be found at every pharmacy for half that. It really depends on what age you are, though. People will question you if you're young and buying this stuff. But if you are young, and really interested in making iodine, get your parents to buy this stuff for you. this is an old post ^^ i brought some from Ebay since and it is good quality i keep it in my fridge to make it last longer!
pheby Posted August 11, 2011 Posted August 11, 2011 Hi friends, Carboxylic acids can be straightaway reduced to alkanes using hydrogen iodide in conjunction with red phosphorus. It is a mighty strong reducing agent. So to reduce benzoic acid to toluene, use HI/Red P. Another method, although not so much well known, is to use the Arndt Eistert synthesis to increase the carbon chain of benzoic acid by a -CH2 group. This would make it benzyl carboxylic acid, Ph-CH2-COOH. Now you can perform a decarboxylation using NaOH/CaO to get toluene. If you want to find the suppliers of iodine plz click the link below http://www.chemicalregister.com/find/Find.asp?SearchTy=PName&SearchSu=iodine&SearchKe=AllKey&SearchLo=ALL&x=0&y=0
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