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Author: Subject: The short questions thread (3)
Phthalic Acid
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I'm looking to dissolve cupronickel coins in HCl then use ammonia to precipitate the NiCl2 from solution (as I believe the Cu2+ ions complex with it). My question is: when using hydrogen peroxide as an oxidizer, how much do I need to use in relation to the rest of the equation? Let's say 2 moles of HCl and 1 mole of coins. Do I use 1 mole of H2O2? Any help would be greatly appreciated =)
Mixell
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Nickel also forms an ammonium complex if I'm not mistaken.
The H2O2 tend to decompose to water and oxygen (which mostly escapes from the solution), I suggest just add it in small amounts until all of the metal dissolves (stir between addition of H2O2).
dann2
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Anyone any thoughts on the reaction of Nitrites and Pb3O4 (Minimum) in the presence of Lead Nitrate and Nitric acid?.
It has been stated that Minimum will destroy Nitrites in a Lead Dioxide plating tank.

Hydrogen Peroxide cannot be used as it reacts with Lead Dioxide in the presence of Nitric acid.

Thnaks,
Dann2
Endimion17
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I was always wondering what exactly is a "chlorine bomb". There was a flood of videos depicting dumbasses pouring a liquid over a white solid and then shaking it closed tight. Some bottles blow into their screaming faces, and some blow with a delay.

I had trouble actually finding what are the ingredients (I see no chlorine being added) and the reaction itself. And I've noticed these videos come primarily from USA. I never ever heard someone doing that in Europe.

Thanks...

bonelesss
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chlorine tablets and rubbing alcohol

[Edited on 18-9-2011 by bonelesss]
Endimion17
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Mood: speeding through time at the rate of 1 second per second

You really thought I didn't think of Google and Wikipedia?

What are those "chlorine tablets"?

bonelesss
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chlorine tablets are used in swimming pools.
But reason why it is used i dont know

[Edited on 18-9-2011 by bonelesss]
hkparker
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They are probably <a target="tab" href="http://en.wikipedia.org/wiki/Trichloroisocyanuric_acid">TCCA</a>, <a target="tab" href="http://en.wikipedia.org/wiki/Dichloroisocyanuric_acid">DCCA<a/>, or <a target="tab" href="http://en.wikipedia.org/wiki/Sodium_dichloroisocyanurate">NaDCC</a>. Im not sure of what the mechanism is behind its reaction with isopropanol however, or if chlorine is actually the main gaseous product; the name might come from a misconception.

"Nothing is too wonderful to be true if it be consistent with the laws of nature." -Michael Faraday
Endimion17
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 Quote: Originally posted by bonelesss chlorine tablets are used in swimming pools. But reason why it is used i dont know [Edited on 18-9-2011 by bonelesss]

Disinfection doesn't ring any bells?

 Quote: Originally posted by hkparker They are probably TCCA, DCCA, or NaDCC. Im not sure of what the mechanism is behind its reaction with isopropanol however, or if chlorine is actually the main gaseous product; the name might come from a misconception.

Yeah, that's what I was thinking, but who knows what's inside.
Trichlor, dichlor, or sodium salts. Might even be a hypochlorite...

So it's isopropanol, not ethanol? Isopropanol is a secondary alcohol, therefore less prone to a nucleophilic attack than ethanol. That might put a new perspective on this, if we're dealing with trichlor and similar compounds.
BTW I'm surprised how easy is to obtain isopropanol in large amounts in USA. "Rubbing alcohol"... we use exclusively ethanol for rubbing here. Most people have no idea what isopropanol is.

I don't know whether this is a true chemical reaction between two compounds or just catalysis.

Can anyone try this at home? In a controlled environment, of course.

[Edited on 18-9-2011 by Endimion17]

hkparker
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I"ve thought about doing it and capturing the gas(ses) for observation, however now that I am away from my lab that is not an option. I would be very interested to see the results however.

Rubbing alcohol is isopropanol here, ans it is very easy to get. Ethanol is actually hard to get except in alcoholic beverages and from some chemistry suppliers.

I'm sure anyone more experienced in organic chemistry then I am could offer an explanation, I might open a thread in the o chem section if it hasn't already been done in the past.

"Nothing is too wonderful to be true if it be consistent with the laws of nature." -Michael Faraday
Roger86
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How much mercury could i extract from mercury lamp? Lets assume its 125W one.I want mercury while its still available, since the LED era has started.I read the readily available and it stated i should practice caution, is it because mercury is off the charts toxic, or is there a second source of danger?

Also i believe there are no mercury in modern mercury switches?
Panache
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 Quote: Originally posted by Roger86 How much mercury could i extract from mercury lamp? Lets assume its 125W one.I want mercury while its still available, since the LED era has started.I read the readily available and it stated i should practice caution, is it because mercury is off the charts toxic, or is there a second source of danger? Also i believe there are no mercury in modern mercury switches?

Don't bother with the lamps, by some cinnabar from a minerals supplier, some mercury switches still have hg in them.

barley81
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I can buy 1L of either conc. phosphoric acid or glacial acetic acid. Which do you think would prove more useful in the long run? I have already 4 oz. of both.
AndersHoveland
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If you typically are interested in organic chemistry, it is probably better to go with the acetic. If you work more with oxidizers or inorganic, better to go with the phosphoric.
Phosphoric can also be useful to make HI or HBr, which are both useful reducing agents in organic chemistry. HI, in the absence of water, can fully reduce ketones, removing the oxygen atom.

[Edited on 23-9-2011 by AndersHoveland]
barley81
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Thanks! Acetic acid it is. If I need HBr (solution) I'll make it from sulfuric acid, and I probably won't use HI regularly since iodide salts aren't cheap.
Chemistry Alchemist
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sponification of methyl salicylate and sodium hydroxide

In the reaction of Sodium Hydroxide with and Methyl Salicylate do i need water to dissolve the sodium Hydroxide or can i just mix the the sodium hydroxide straight in to the methyl salicylate. I want to evaporate teh Methanol that forms with minimal to no water, and i cant distill off the methanol because i dont have the right glassware to do so.

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Just mixing should work, leaving you (ultimately) with sodium salicylate and methanol. But I actually see no reason not to add water... what is your objection to applying a little heat to drive off the water? Sodium salicylate should be stable to quite a bit over 100C, and you could dry it in a short time at a mere 60C.
Note that what you are doing is not saponification, as your starting material is not a triglyceride. It is base-catalyzed hydrolysis. And be aware that concentrated NaOH can etch glass.
Chemistry Alchemist
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in the reaction, does it produce any water at all or not? can i dry the methanol with sodium hydroxide or magnesium sulfate? i cant heat anything... i can only use the sun really :/ im planning on investing in lab ware, i really really do need more then what i have... im pretty sure sodium salicylate is more soluble in methanol right?

Steve_hi
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seperating calcium sulfate from ammonnium nitrate

Hi hope this is the right place.
I am working on getting ammonium nitrate from fetilizer 27-0-0
I was told to mix it with water and decant it which i have done
now today I read from a previous reply to my post that I may have calcium sulfate mixed in is there a way to seperate the calcium sulfate from the ammonium nitrate and how can I test the ammonium nitrate for immpurities my immidiate use for some NH4NO3 will be to make some nitric acid.
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Filtering a hot, saturated solution of AN and cooling will precipitate fairly clean crystals.
But alkali metal nitrates are preferred for NA production because AN is subject to oxidation in hot H<sub>2</sub>SO<sub>4</sub>.

Chemistry Alchemist
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If your just trying to separate Calcium Sulfate from Ammonium nitrate then just add enough water the the batch, Ammonium nitrate is easily soluble and will dissolve but the Calcium Sulfate is insoluble in water and can be decanted as you said, to remove some impurity, just add methanol to the AN, AN is soluble in Methanol and will leave behind any other impurity. then you can recrystillise the batch to obtain a better product

solo
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.......CH3CH[NH2COCH3]CH3 how can i remove the acetyl group attached to the amine....Or reduce it to a methyl group....thanks for any tips, i have looked but not sure,......solo

P.S. ....i've read where hydrolysis will do it, can it be decarboxylated to leave the methyl group

[Edited on 9-10-2011 by solo]

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fledarmus
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Deacetylation of amines has always been a challenge. Strong acids and bases with heat will both work, but they tend to chew up the rest of the functional groups in your molecule as well. Doing a Google Scholar search for deacetylation of amines will show quite a few exotic attempts to do this, since it shows up frequently in protein synthesis.
mr.crow
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Is hexamine soluble in dichloromethane? I only found information for chloroform

Double, double toil and trouble; Fire burn, and caldron bubble
Chemistry Alchemist
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Identifying Chromate salts

I recently extracted a chromium compound from pigment paint, its a Bright yellow salt... its either Strontium or Barium Chromate, how can i test? i know if i can get it to chloride or something and burn it, it will produce either red or green but how would i remove the chromium from the strontium or barium if u know what i mean?

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 Sciencemadness Discussion Board » Fundamentals » Miscellaneous » The short questions thread (3) Select A Forum Fundamentals   » Chemistry in General   » Organic Chemistry   » Reagents and Apparatus Acquisition   » Beginnings   » Responsible Practices   » Miscellaneous   » The Wiki Special topics   » Technochemistry   » Energetic Materials   » Biochemistry   » Radiochemistry   » Computational Models and Techniques   » Prepublication Non-chemistry   » Forum Matters   » Legal and Societal Issues