Chemical Forums
Chemistry Forums for Students => High School Chemistry Forum => Topic started by: asadc12 on November 26, 2009, 06:26:54 PM
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I am just curious how could make Na Cl (salt) ?
My friend told me you could by mixing Sodium Phosphate and Iron chloride.
Can you guys tell me any more ways that I could make Na Cl except Sodium Phosphate and Iron chloride?
a balanced equation would help me understand :)
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Weird idea to make kitchen salt. ::)
It is more expensive to prepare than just buy a kilo from your local store. :-\
If you want to make some of it anyway, there are many possibilities. The easiest one I can think of is to react hydrochloric acid and sodium hydroxide:
NaOH + HCl :rarrow: NaCl + H2O
You have to do this reaction in water (or else, HCl would be a gas). At the end, you need to evaporate water to get your product.
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aw I just figured that out :(
Are there any other ways
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Yes.
If one of the salts forming is insoluble, it will precipitate. You just have to filter it off and evaporate water to get NaCl.
For example, reactions in water:
* 2NaI + PbCl2 :rarrow: 2NaCl + PbI2
PbI2 has a low solubility in water. So you filter it out and you're left with salty water (and still some traces of Pb2).
* Na2SO4 + BiCl2 :rarrow: 2NaCl + BiSO4
BiSO4 will precipitate.
* Na2(oxalate) + CaCl2 :rarrow: 2NaCl + Ca(oxalate)
Calcium oxalate is damn insoluble in water.
If you don't want to use water, you can use sodium metal or hydride:
* Na0 + Cl2 :rarrow: 2NaCl
This reaction is between a solid and a gas, so it will react only at the sodium surface.
* NaH + HCl :rarrow: NaCl + H2
Hydrogen is a gas that just flies away
* NaNH2 + HCOCl :rarrow: NaCl + HCONH2
You could use an acyl chloride and sodium amide.
There are many many other ways. But the easiest way is to go buy it. No bother making it ;D
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Benzene diazonium chloride + Ethylsodium
C6H5N2Cl +NaC2H5--> NaCl + C6H5C2H5
hydrazinium chloride + NaOH
N2H5Cl +NaOH-->N2H2 +NaCl +H2O
1-chlorobutane + sodium nitrite
C4H9Cl+NaNO2--> C4H9NO2 +NaCl
2 Sodium azide + cyanogen chloride
2NaN3 + CNCl --> NaCl + NaCN7 ;) (yes, CN7 is correct before anyone asks)
2Na +Cl2--> 2NaCl
Possibilities are infinite
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2 Sodium azide + cyanogen chloride
2NaN3 + CNCl --> NaCl + NaCN7 ;) (yes, CN7 is correct before anyone asks)
NaCN7?! :o :o :o
I've never seen this one before, and it looks interesting. What is its structure?
I tried to guess:
CNCl + N3- will form a 5-chloro-tetrazolate compound, like the picture of a tetrazole ring below with one added chlorine attached on the carbon.
(https://www.chemicalforums.com/proxy.php?request=http%3A%2F%2Fwww.adeviq-spin.com%2Ftetrazole.gif&hash=d30b6a566aecd7f748f2e90cc8185c79fe0bf1b1)tetrazole ring
But then, I don't see where a second N3 would react to form CN7-. I couldn't find it in SciFinder.
Thanks for this unusual compound :D
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Azidotetrazole, a sexy beast of a compound. :-* :-* :-* :-*
First equiv of azide makes cyanogen azide
second equiv cyclizes to azidotetrazole.
;D :D ;D :o ;D :D ;) :)
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http://pubs.acs.org/doi/abs/10.1021/ja8077522
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Nice, thank you. I see I had guessed half of the compound. 8)
It would be nice to use as a ligand to complex transition metals, but its instability is a big problem. Nevermind, it keeps me thinking about ligands possibilities. :)
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Nitrotetrazole exists as a ligand in many metal complexes
Ex :
Fe(NT)6 (4-) (sodium and ammonium salts)
Co(NH3)4(NT)2 ClO4 "BNCP"
Both are primary explosives of high quality. ;)
Azidotetrazole complexes likely far too unstable :'(
Even when large alkyl chains are hung off azidotetrazole, it is still exceeding impact, friction and spark sensitive, and this is after severely diluting the nitrogen content.
General trend for 5-substituted tetrazole explosiveness: more electron withdrawing, more sensitive :)
N2+ (explode above 2% concentration in aqueous solution :'( ) >N3 > NO2 >NNO2 >NH2
:D