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Relative mass of lithium
Relative mass of lithium
Relative mass of lithium
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Recommended: Relative mass of lithium
Determination of Relative Atomic Mass of Lithium
Evaluation:
In general the accuracy of the experiments was good. However with
practice, the accuracy could be improved; accuracy being how close the
results are to the real answer. I think I have carried pit the
experiment as well as I possibly could at the time with the given
conditions and time period allowed. I have gained precise results from
the practical. However, looking back at the analysis section, the
relative atomic mass values I found were not exactly 6.9 as presented
in the periodic timetable. Method (1) gave me 8.28; a difference of
1.38 and method (2) gave me 7.37, a difference of 0.43 to the
real/reference value. Therefore method (2) proved to be more accurate.
Overall the results were good and came close to the real values. There
were no anomalous results.
Limitations:
The main sources of error that I found to be evident and which were
out of my control were as follows:
* In method (1), due to the oil that lithium is stored in, not only
caused problems with weighing it, but also when I attempted to
quickly put pieces of lithium into the chonical flask with
distilled water, some pieces "stuck" on the weighing boat, sue to
residue oil having a "sticky" effect. This caused a delay in the
whole process and I was not able to place the bung in place
immediately, thus hydrogen was lost making the gas collected less
than what it was supposed to be.
* When weighing lithium the percentage error was:
(0.00005/0.00645) x 100= +or- 0.775%
Therefore the error possible caused by the weighing scales by default
is very low;...
... middle of paper ...
...ll be clearer when the reaction is complete, thus more
concurrent results will be produced. Clearly there is also a need
for a control, although it was initially thought that it was very
obvious when the solution turns colourless, this practical has
shown that a control would be useful to compare the colours.
However the other problem of the solution returning to a slight
pink colour can be eliminated by waiting for this to occur, and
when it does, titrate it further opening the burette very
slightly, allowing acid to be added more slowly into the solution.
Carrying out titrations is a skill that develops with practice,
more repetitions will lead to improved results, both in accuracy
and precision.
Both methods are the most accurate, considering the equipment
available.
Solid A was identified to be sodium chloride, solid B was identified to be sucrose, and Solid C was identified to be corn starch. Within the Information Chart – Mystery White Solid Lab there are results that distinguishes itself from the other 4 experimental results within each test. Such as: the high conductivity and high melting point of sodium chloride, and the iodine reaction of corn starch. Solid A is an ionic compound due to its high melting point and high electrical conductivity (7), within the Information Chart – Mystery White Solid Lab there is only one ionic compound which is sodium chloride, with the test results of Solid A, it can be concluded that is a sodium chloride. Solid B was identified as sucrose due to its low electrical
...ost likely to be battery acid. If it is water, it has a Ph level of around 7. For vinegar, the Ph level is approximately 2.4 - 3.4. Thus, once testing the liquid compare it with the Ph levels above to discover the mystery solution.
Once the mixture had been completely dissolved, the solution was transferred to a separatory funnel. The solution was then extracted twice using 5.0 mL of 1 M
Okay, if our lithium weight is going to be 6.941 g/moL Then that means we have to take 24.6g of Lithium and multiply it by 1 mol of Lithium over 6.941 g of Lithium. This would equal to be 3.544 mol of Lithium. Then we have to take that 3.544 and multiply it by 1 mol of hydrogen gas over 2 mol of lithium. Which would then equal into 1.772 mol of hydrogen gas. We can then figure out that 1.772 is our “n”. The “T” is our 301 Kelvin, the “P” is our 1.01 atm and the “R” is our 0.0820 which would be the L atm over mol k. And we can’t forget about our “V” which would be V equals nRT over P which equals 1.772 mol divided by 0.0820 L atm over mol kelvin multiplied by 301 kelvin over 1.01 atm which equals to our final answer of: 43.33 of H2
It is important however to note that the NH4 and K ions are still in
Since its discovery, lithium has been primarily used in batteries, in chemical synthesis, and in alloys and glass. Although lithium is used in everyday things we use, l...
Ionic liquids (ILs) are liquids composed entirely of ions. Molten salt is the term normally reserved for those systems that are liquid at high temperatures, for example NaCl (table salt is a liquid at ≈ 800 0C). Room-temperature ILs are liquid below 100˚C, have received considerable attention as substitutes for volatile organic solvents. Due to their remarkable properties, such as negligible vapour pressure, large liquidous range, high thermal stability, good ionic conductivity, high electrochemical stability, they are considered favourable medium candidates for chemical syntheses. ILs are usually categorized into four types based on their cation segment: 1) alkylammonium-, 2) dialkylimidazolium-, 3) phosphonium- and 4) N-alkylpyridiniumbased ILs (Figure 1). Ionic liquids are generally composed of a bulky organic cation, such 1-butyl-3 methylimidazolium and typically an inorganic anion such as a halide. Below are the chemical structures of some common cations and anions used to make ILs.
Blister copper then goes through the fire refining and then cast into copper anodes and placed in an electrolytic cell. Each copper anode is placed in a tank made of concrete. A sheet of copper is placed on the opposite end of the concrete tank to become the cathode or the negative terminal. An acidic copper sulfate solution is then poured into the concrete tanks; this forms the e...
This was allowed to mix for a few minutes; a little excess water was used to ensure that sodium bromide was fully dissolved. This mixture was placed in an ice bath while continuing to stir. 1.3 ml (24.39 mmols) of concentrated sulfuric acid was added dropwise. The flask was removed from the ice bath and heated to reflux for 1 hour while continuing to stir. The resulting top layer was transferred to a conical vial in which 1.5 mL (22.51 mmols) of 80 % sulfuric acid was added. 2.0 mL of water was added to allow a layer to form. The bottom layer was removed and transferred to another conical vial in which 2.0 mL of saturated sodium bicarbonate was added. The bottom, organic layer, was transferred to a conical vial. Calcium chloride, a drying agent, was used to collect the remaining aqueous layer that
Determining the Relative Atomic Mass of Lithium An experiment has been carried out to determine the relative atomic mass of Lithium by using two different types of methods The first method that was carried out was to determine the volume of Hydrogen produced. In this experiment a fixed amount of Lithium was used, in my case it was 0.11g. At the end of this experiment, the volume of Hydrogen gas I collected was 185cm³. Then using the solution of lithium hydroxide made from experiment one, I used it in the titrating experiment, to find out the total volume of Hydrochloric acid used to titrate the lithium hydroxide. RESULTS TABLE Experiment Initial Volume ( cm³) Final Volume ( cm³) Total volume Of HCl used ( cm³) Rough 0.2 30.3 30.1 1 6.3 35.8 29.5 2 2.7 32.0 29.3 Average 29.6 CONCLUSION Method 1 [IMAGE]2Li (s) + 2H20(l) LiOH(aq) + H2(g) Number of moles of Hydrogen. Volume of hydrogen gas was 185 cm³. Weight of Lithium was 0.11g. N = __V__ _185_ = 0.0077 MOLES 24000 24000 Number of moles of Lithium.
Following the aforementioned procedure, the neutral compound was to be isolated from the ether solution. Moved to a clean flask, the ether solution was introduced to anhydrous sodium sulfate. After letting the mixture sit for about 10 minutes, the mixture was decanted into a new beaker. The ether in this final mixture was allowed to evaporate, leaving behind the neutral compound. Percent recovery was recorded and the compound was transported to a vial.
Each scientist or team of scientists had so much trouble reducing the Lithium compounds because Lithium does not exist in its elemental form in nature. It combines very easily with other elements. Lithium is a soft silvery-white lustrous metal, which can be easily cut with a knife, and it is the lightest of all known metals. It is highly reactive with water and air, and tarnishes readily when exposed to the latter due to a formation of a layer of Lithium suboxide on its surface. Because of its high rate of reaction to air, it must be stored under liquid paraffin, oil, or kerosene, which contain no air, to prevent oxidation. Lithium is detected in its compounds by the characteristic red coloration that it imparts to flames when burned, as Gmelin detected, and by spectroscopic methods.
strong base ( contained OH ) were 100% ionized in water and they were all
On repeating this experiment more care should be taken when purifying to remove the solvent impurities and minimise loss of crude product.
...ations served as background information for the calculations and for the general procedure of the lab. The solid acid, when added to water ionized to form charged particles causing the solution to have a certain pH that could be figured out from a titration curve graph. The acid used in this lab, KHP, ionized in water and formed Hydronium ions in the water. These ionized particles were what gave the acid a certain pH and those particles were what was being neutralized in the reaction. Multiple titrations were performed to neutralize the acid, in each titration, the lab groups attempted to reach the exact endpoint of the reaction without going over it. The endpoint was indicated by a slight color change in the solution to a pale pink color. When the endpoint was achieved, the calculations for the moles of acid to the moles of base were equal at that point.