Forensics C

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Re: Forensics C

Post by Dragonshark »

scm424 wrote:NH4Cl is supposed to turn dark blue with benedict's solution (some type of copper complex ion forms. [Cu(NH3)4]2+ maybe? Nevertheless, it still is dark blue). It is kind of hard to tell sometimes though. I suggests filling up a test tube with the same amount of water as the NH4Cl solution test tube and then add the same amount of benedict's solution to each test. This way, you can tell if one is more blue than the other.
Phenylethylamine wrote:This. Definitely this. For relatively subtle color changes, always compare side by side.

And salcedam is correct, you do not need to heat the mixture to see this effect; the reaction between ammonium chloride and Benedict's occurs at room temperature.
Thanks again. I'll have to retry this tomorrow.
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Re: Forensics C

Post by Phenylethylamine »

Dragonshark wrote:Thanks again. I'll have to retry this tomorrow.
You're quite welcome.

Only peripherally related: Has anyone else noticed how few people seem to know how to use Benedict's?

At my Regionals last year (and okay, it's Regionals, but still), we were the only team that actually left the test tube with Benedict's (and what turned out to be glucose) in the hot water bath for more than maybe ten seconds. There was one communal hot water bath at the back of the room, and we asked the event supervisors if we could leave our test tube in there for a little while and go back to our lab station; they gave us this surprised/approving look, since apparently nobody else had thought to leave it in there for long enough for this to be relevant. There were a couple teams near the back that saw ours turn orange and got rather worried, since they hadn't found any glucose...

I was familiar with Benedict's solution from doing Food Science years ago, and I know that if you have a food sample that contains a relatively small amount of a reducing sugar, it can take up to ten minutes for the qualitative test to show anything. With pure glucose, it only took a minute or so, but still, you had to wait. Are there some instructions out there that are leading people to believe it's an instantaneous test?
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Re: Forensics C

Post by AlphaTauri »

Phenylethylamine wrote:I was familiar with Benedict's solution from doing Food Science years ago, and I know that if you have a food sample that contains a relatively small amount of a reducing sugar, it can take up to ten minutes for the qualitative test to show anything. With pure glucose, it only took a minute or so, but still, you had to wait. Are there some instructions out there that are leading people to believe it's an instantaneous test?
Perhaps the fact that NH4Cl turns deep blue immediately with Benedict's is leading people to think that glucose will turn orange immediately as well?

Also, does KCl turn green with Benedict's + heat? I've seen it written in our old forensics notes, but I haven't been able to find confirmation nor get the lab time to test it out.

Edit: Although Wikipedia does say that Benedict's can form a green precipitate...
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Re: Forensics C

Post by Phenylethylamine »

AlphaTauri wrote:
Phenylethylamine wrote:I was familiar with Benedict's solution from doing Food Science years ago, and I know that if you have a food sample that contains a relatively small amount of a reducing sugar, it can take up to ten minutes for the qualitative test to show anything. With pure glucose, it only took a minute or so, but still, you had to wait. Are there some instructions out there that are leading people to believe it's an instantaneous test?
Perhaps the fact that NH4Cl turns deep blue immediately with Benedict's is leading people to think that glucose will turn orange immediately as well?
I don't know, I always assumed that use of Benedict's was less well known than using it to test for reducing sugars.
AlphaTauri wrote:Also, does KCl turn green with Benedict's + heat? I've seen it written in our old forensics notes, but I haven't been able to find confirmation nor get the lab time to test it out.

Edit: Although Wikipedia does say that Benedict's can form a green precipitate...
From a quick google search, I'm seeing that KCl will turn Benedict's green (not a green precipitate, green solution) because it reacts with copper(II) sulfate to make [CuCl4]2- ions, which are green in solution. KF would make a green precipitate, because CuF2 is insoluble and green, but KF is not on the list.

I don't see anything about heat, just that you add aqueous KCl to aqueous CuSO4 (AKA the main ingredient of Benedict's solution).
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Re: Forensics C

Post by salcedam »

AlphaTauri wrote:
Phenylethylamine wrote:I was familiar with Benedict's solution from doing Food Science years ago, and I know that if you have a food sample that contains a relatively small amount of a reducing sugar, it can take up to ten minutes for the qualitative test to show anything. With pure glucose, it only took a minute or so, but still, you had to wait. Are there some instructions out there that are leading people to believe it's an instantaneous test?
Perhaps the fact that NH4Cl turns deep blue immediately with Benedict's is leading people to think that glucose will turn orange immediately as well?

Also, does KCl turn green with Benedict's + heat? I've seen it written in our old forensics notes, but I haven't been able to find confirmation nor get the lab time to test it out.

Edit: Although Wikipedia does say that Benedict's can form a green precipitate...
With respect to the confusion about Benedict's and glucose, I think people just don't know how long to wait because the reaction time can vary and they may have done previous tests where the orange precipitate formed almost instantaneously (perhaps 30 seconds or so). The most I had to wait for a solution of glucose and Benedict's to react was about 4 minutes. Not sure why it took that long...perhaps the water wasn't hot enough...

According to the dichotomous key the Woz has, KCl does turn Benedict's green WITH heat.
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Re: Forensics C

Post by Phenylethylamine »

salcedam wrote:
AlphaTauri wrote:
Phenylethylamine wrote:I was familiar with Benedict's solution from doing Food Science years ago, and I know that if you have a food sample that contains a relatively small amount of a reducing sugar, it can take up to ten minutes for the qualitative test to show anything. With pure glucose, it only took a minute or so, but still, you had to wait. Are there some instructions out there that are leading people to believe it's an instantaneous test?
Perhaps the fact that NH4Cl turns deep blue immediately with Benedict's is leading people to think that glucose will turn orange immediately as well?

Also, does KCl turn green with Benedict's + heat? I've seen it written in our old forensics notes, but I haven't been able to find confirmation nor get the lab time to test it out.

Edit: Although Wikipedia does say that Benedict's can form a green precipitate...
With respect to the confusion about Benedict's and glucose, I think people just don't know how long to wait because the reaction time can vary and they may have done previous tests where the orange precipitate formed almost instantaneously (perhaps 30 seconds or so). The most I had to wait for a solution of glucose and Benedict's to react was about 4 minutes. Not sure why it took that long...perhaps the water wasn't hot enough...
True; and given that almost all the reactions involved in this event occur more or less immediately, it's not a ridiculous assumption to make. I just would have expected more people to do some minimal reading about the reagents in the rules before the event :-P
salcedam wrote:According to the dichotomous key the Woz has, KCl does turn Benedict's green WITH heat.
Thanks. I didn't see this information anywhere. Also, "the Woz"?
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Re: Forensics C

Post by salcedam »

Phenylethylamine wrote:
salcedam wrote:According to the dichotomous key the Woz has, KCl does turn Benedict's green WITH heat.
Thanks. I didn't see this information anywhere. Also, "the Woz"?
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Re: Forensics C

Post by Dragonshark »

I redid the reaction between ammonium chloride and Benedict's today, and there is indeed a slight, but noticeable color change. A basis for comparison IS needed, though.
salcedam wrote:According to the dichotomous key the Woz has, KCl does turn Benedict's green WITH heat.
I'll have to try this soon and see what happens.

Also, does anyone know what the general difference(s) between dog and horse hair are when looking at them in a microscope (light and/or electron)? I asked this question awhile back, but to little avail.
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Re: Forensics C

Post by Phenylethylamine »

salcedam wrote:
Phenylethylamine wrote:
salcedam wrote:According to the dichotomous key the Woz has, KCl does turn Benedict's green WITH heat.
Thanks. I didn't see this information anywhere. Also, "the Woz"?
Linda Wozniewski, the National Director for Forensics. xD

If you go to the soinc.org website, her website has useful information regarding chem events such as Crime Busters, Forensics, etc. One of the links in the Forensics section of the SO Inc. website is to her website. ^.^
Ah yes, I think I've used some of her resources before, but I was not on a nickname basis with her xD (and also apparently missed her dichotomous key... maybe because I already had my own made up by the time I found that site).
Dragonshark wrote:I redid the reaction between ammonium chloride and Benedict's today, and there is indeed a slight, but noticeable color change. A basis for comparison IS needed, though.
Thank you, this is good to know.
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Re: Forensics C

Post by Phenylethylamine »

I did my own tests with Benedict's today: ammonium chloride, potassium chloride, and lithium chloride (because it occurred to me that lithium chloride would probably react the same way with copper(II) sulfate as potassium chloride would).

With ammonium chloride, upon mixing it with Benedict's, I saw an almost immediate and quite noticeable color change – an almost indigo-y dark blue. I didn't need a basis of comparison to see the change; I recommend using more of the powder (and rather than making a solution of the powder and then adding Benedict's, try just dissolving the powder directly in Benedict's).

With lithium chloride, upon mixing it with Benedict's and placing the test tube in a hot water bath, I saw a color change at the end of the test tube after about thirty seconds (lime green). It was pretty easy to see, but definitely localized at the bottom of the tube.

With potassium chloride, same procedure as lithium chloride, I got nothing, even after about ten, fifteen minutes. I assume that under the right conditions (more potent Benedict's? More powder? Higher heat? Longer time?) you could get some green in there, and it would presumably look quite similar to what I got for lithium chloride, but it'll definitely be a slower/less noticeable reaction than the LiCl.

Also, not really related but another thing I noticed today: always make sure you're comparing your pH paper against one dipped in plain water as a control. On a practice event today, I had some weak acid/weak base powders that I misidentified as neutral and therefore ended up going down the wrong path of my key. I was using pretty lousy pH paper, not the stuff I use in competition, but still.
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