ATAR Notes: Forum
VCE Stuff => VCE Science => VCE Mathematics/Science/Technology => VCE Subjects + Help => VCE Chemistry => Topic started by: danielf on March 02, 2008, 11:47:42 am
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New to the site and hopin someone could lend a hand for my first SAC. Part 1 is a gravimetric analysis, one of the questions is 'why does the crucible have to be cool when weighed?' I've been told it has something to to with water adsorption to the porcelain however some more definite explanations would be greatly appreciated.
Thanks heaps
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My gut feeling here is that a hot crucible would damage the scales; electronic scales are very sensitive, and putting a hot crucible on it would be a no-no. The crucible is heated to remove any water content in the salt, sure, but keeping the water out would require a desiccator rather than a cool crucible.
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The crucible has to be cooled to room temperature because if it was still hot, the higher temperature would cause air currents around the balance, giving inaccurate results.
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Good point, thanks
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Wot questions would u expect to be on a PRAC SAC involving, finding the sulfate content in fertiliser by the means of gravimetric analysis (I don't mean conclusion, obervation, aim...etc)?
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Possibly questions about the procedure such as:
Why does the precipitate need to be washed?
Why was an excess of barium chloride solution added?
Why must the precipitate be heated to constant mass?
List two reasons why barium sulfate is a suitable product in this gravimetric anaysis?
Also, calculations based on results, and writing an ionic equation for the reaction.
Hope this is helpful. :)
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There will probably be a question on sources of uncertainty too. make sure you write about possible impurities in the lawn feed (may form additional precipitate) as well as the various forms of mechanical losses. Also, if the precipitate was formed rapidly, some of the solution (water) may have become trapped in the crystal grain structure of the precipitate (thus inreasing its weight).
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i noe the observation part of the prac is usually one of the most easily parts to write, but for this prac i just don't noe wot 2 write. i mean there wasn't that much to observe except for the colour change and weight change, which is already in my results section. Wot do u think i should note. my prac is on http://resources.mhs.vic.edu.au/chemistry/year12/3pracproc.pdf , its this first and thrid prac (we're doing a combined prac, how fun).
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1. Lawn fertiliser contains nitrogen. A 1.3g sample of lawn fertiliser was weighed and carefully transferred to a 250ml volumetric flask. The weighing bottle was washed with a little de-ionised water and added to the content, until it reached the calibration line. A 20ml aliquot of this solution was added to a flask containing 20ml of .1M sodium hydroxide solution. 50ml of de-ionised water was than added. The flask was heated until the reaction NH4+ (aq) +OH-(aq) = NH3 (aq) +H20) (l) was complete. The burette was than titrated with .1M hydrochloric acid, using methyl red as indicator. The end point was reached when 44.3ml had been added.
Calculated the amount of NH4+ ions in the 1.3g fertiliser sample and the percentage by mass of nitrogen in the fertiliser, assuming all the nitrogen is present as ammonium ions.
2. 1.4g of ground fertiliser was placed in a 100ml beaker. 50ml of de-ionised water was added and filtered into a 600ml beaker. 3ml of 2M hydrochloric acid and water was added, until the total volume was 200ml. The solution was than boiled and 15ml of .5M barium chloride solution was added drop by drop. The precipate was colected filtrated, dried and weighed. A mass of 1.56g was obtained. How do u find the proportion of sulfate in the fertiliser?
(Can u plz show working?) thanks so much
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Question 1
First, recognise that after the preparatory reaction (the given reaction), we are left with a base: NH3.
Strategy:
- Calculate the number of mole of hydrochloric acid consumed per aliquot.
- Realise there will be no excess
, hence ammonia will react with hydrochloric acid.
- Write an equation for the reaction between hydrochloric acid and ammonia (acid + base).
- Hence, find the number of mole of ammonia that is present per aliquot.
- Using this, calculate the number of mole of ammonium present (using the given reaction) per aliquot.
- Scale this number to the number of moles of ammonium present in the 1.3 gram sample.
- Hence find the mass of nitrogen (N only), and the percentage mass of nitrogen
Solution:
} = 0.0443\times 0.1 = 0.00443\mbox{ mol})
There is no excess
, because it is all neutralised with the ammonium, so the reaction that takes place is:
Chemical equation: 
}_{\mbox{aliquot}} = \mbox{n(NH3)} = \mbox{n(HCl)} = 0.00443\mbox{ mol})
}_{\mbox{sample}} = 0.00443 \times \frac{250}{20} = 0.0554\mbox{ mol})
} = \mbox{n(NH4}^+\mbox{)} \times \mbox{M(N)} = 0.0554 \times 14 = 0.775\mbox{ g})
})
(It should be 1 significant figure, but since that's ridiculous, I've given it to three)
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Question 2
To find the proportion of sulfate in the fertiliser, you recognise that
will precipitate upon addition of barium chloride. We should assume that this is the sole precipitate (as we do in any gravimetric analysis - an implicit assumption that most people overlook), and therefore that:
} = 1.05\mbox{ g})
No "un-dilutions" need to take place as was the case in question 1, because the entire sample was used (wasn't split up into aliquots). Therefore, we can go straight ahead and calculate how much sulfate there is:
} = 1.05 \times \frac{\mbox{MW(SO}_4\,^{2-}\mbox{)}}{\mbox{MW(BaSO}_4\mbox{)}} = 1.05 \times \frac{96.1}{233.4} = 0.432\mbox{ g})
This gives us the proportion of the mass which is solely sulfate, and hence we can find the percentage mass of it:
})
I hope I'm right, I've got a massive headache today :(
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thanks coblin
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looking back, i think u made a mistake. For the step where u had to - Scale this number to the number of moles of ammonium present in the 1.3 gram sample- isn't the molar mass of NH4+ 18?
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Nah, you're supposed to find the mass of nitrogen only. I sort of skipped the obvious step: