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Essay about thin layer chromatography
Essay about thin layer chromatography
Essay about thin layer chromatography
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In this experiment, column chromatography and thin layer chromatography were used to separate a mixture of fluorene and 9-fluorenone. These two methods were then compared, and the results were analyzed. In column chromatography, 0.1010 g of mixture was separated. During the separation, fluorene eluted first. This compound was white in color once dried with the rotary evaporator. A percent yield of 93.47% was calculated for fluorene. The product that eluted first was confirmed to be fluorene by the IR spectrum obtained and the experimental melting point. The IR spectrum RM-02-CC1 was the spectrum obtained for this compound. Aromatic carbon- hydrogen bonds, carbon-carbon double bonds and hydrogens attached to sp2 carbons were shown by peaks 3038 …show more content…
The IR spectrum RM-02-CC2 was obtained. The spectrum consisted of a carbonyl peak, an aromatic carbon-carbon double bond peak, and a sp2 hybridized carbon and hydrogen bond peak at 1713, 1598, and 734. These functional groups are all present in 9-flourenone. The carbonyl group specifically was important because fluorenone was the only that contained a carbonyl group. The Identity was further confirmed by the melting point, 79-80˚C. This value is similar to the known value 84˚C2. The melting point observed during the experiment is greater than the known because the sample is slightly impure. This impurity is caused by presence of fluorene on the tip of the columns. As stated before, the tip of the column needs to be manage to ensure pure products. The presence of fluorene would increase the temperature as seen in the melting point results because the melting point of this compound is greater than fluorenone. Overall, both compounds were separated with column chromatography and presented reasonable yields for both products. Column chromatography is a useful technique to separate mixtures with both large and small quantities. Unlike TLC, column chromatography and be used for large amounts of
Fluorescence measurement provides very important information about the photochemistry of a particular molecule. The first part of this experiment was dealing with the fluorescence behavior of a Leucophor PAF. Information from both spectrophotometry and fluorimetry was used to measure the quantum yield as well as to explain why Leucophor PAF was use as commercial optical brightener. The second part of this experiment dealing with fluorescence quenching of quinine bisulphate solution (QBS) is the presence of sodium chloride.
The isomerization procedure was done in order to create dimethyl fumarate from dimethyl maleate. Dimethyl maleate and dimethyl fumarate are cis and trans isomers, respectively. This procedure was done via a free radical mechanism using bromine. The analysis of carvones reaction was done in order to identify the smell and optical rotation of the carvone samples that were provided. The odor was determined by smelling the compound and the optical rotation was determined using a polarimeter.
The primary goal of this laboratory project was to identify an unknown compound and determine its chemical and physical properties. First the appearance, odor, solubility, and conductivity of the compound were observed and measured so that they could be compared to those of known compounds. Then the cation present in the compound was identified using the flame test. The identity of the anion present in the compound was deduced through a series of chemical tests (Cooper, 2009).
The IR spectrum that was obtained of the white crystals showed several functional groups present in the molecule. The spectrum shows weak sharp peak at 2865 to 2964 cm-1, which is often associated with C-H, sp3 hybridised, stretching in the molecule, peaks in this region often represent a methyl group or CH2 groups. There are also peaks at 1369 cm-1, which is associated with CH3 stretching. There is also C=O stretching at 1767 cm-1, which is a strong peak due to the large dipole created via the large difference in electronegativity of the carbon and the oxygen atom. An anhydride C-O resonates between 1000 and 1300 cm-1 it is a at least two bands. The peak is present in the 13C NMR at 1269 and 1299 cm-1 it is of medium intensity.
A weak peak was at a position between 1600-1620 cm-1 can also be seem in the IR, which was likely to be aromatic C=C functional group that was from two benzene rings attached to alkynes. On the other hand, the IR spectrum of the experimental diphenylacetylene resulted in 4 peaks. The first peak was strong and broad at the position of 3359.26 cm-1, which was most likely to be OH bond. The OH bond appeared in the spectrum because of the residue left from ethanol that was used to clean the product at the end of recrystallization process. It might also be from the water that was trapped in the crystal since the solution was put in ice bath during the recrystallization process. The second peak was weak, but sharp. It was at the position of 3062.93 cm-1, which indicated that C-H (sp2) was presence in the compound. The group was likely from the C-H bonds in the benzene ring attached to the alkyne. The remaining peaks were weak and at positions of 1637.48 and 1599.15 cm-1, respectively. This showed that the compound had aromatic C=C function groups, which was from the benzene rings. Overall, by looking at the functional groups presented in the compound, one can assume that the compound consisted of diphenylacetelene and ethanol or
To remove the impurity, the fluorene had to be recrystallized and purified. In an aside step, 15 mL of ethanol was heated until the solvent was boiling. Ethanol is the ideal solvent to crystallize fluorene, because it is polar. Though fluorene is nonpolar, fluorene is not too soluble or insoluble in ethanol. The decision for selecting this solvent came from past experimentations as well. At first, methanol would have been a good solvent for fluorene, but methanol evaporates very quickly. A greater amount of methanol would have been required to dissolve the impure fluorene, but a little amount of ethanol is only needed to dissolve the impure fluorene completely. Once the ethanol solvent was boiling, a small amount was added to the flask, just enough to cover the impure fluorene solids. That flask was then heated on a hot plate, and additional hot ethanol was added continuously until the fluorene completely dissolved (10). As soon as the solid dissolved, the flask was stoppered and placed into an ice-water bath (11). Crystallization happened almost
Separations are important techniques in chemistry that are used to separate various components of a mixture. They are carried out by mixing two immiscible liquids containing certain solutes together in a separatory funnel, allowing them to separate, then extracting the distinct layers that form. The ratio of the concentration of solute present in the upper layer to the concentration in the lower layer is called the partition coefficient. The efficiency of a separation is described by this partition coefficient. If the coefficients for the two layers are largely different, then the separation can be carried out in a single step. If they aren’t, a more complex process is necessary.1,2 Countercurrent chromatography is a technique used carry out separations in these kinds of cases. It uses a continuous liquid-liquid partitioning process to streamline the usual extraction procedure.
Rogers, D. H.; Morris, J. C.; Roden, F. S.; Frey, B.; King, G. R.; Russkamp, F. W.; Bell, R. A.; Mander, L. N. Pure Appl. Chem., 1996, 68, 515.
The purpose of this particular experiment is to acquire the product 4-methylcyclohexene from the reactant 4-methylcyclohexanol by altering the equilibrium and using an elimination (E1) reaction involving dehydration with a strong acid acting as a catalyst. The following techniques and analyses were utilized in this experiment: simple distillation, “salting-out” the crude product, neutralization, unsaturation test, and infrared spectroscopy. Simple distillation is necessary for separating a liquid mixture and collecting the purified product or desired result. “Salting-out” the crude product was employed as a means of an extraction and purification process; that is, the salt would extract the water from the mixture, which leads to a reduction in solubility of the organic compound.
The purpose of this experiment is to learn how to use fractional distillation to separate a mix of isopropyl acetate and toluene, redistill them, and use gas chromatography to examine the separation.
The crude extract obtained by solvent extraction was subjected to various qualitative tests to detect the presence of common chemical constituents as:
The Thin layer chromatography is one of the oldest techniques which is used to identify what is present in an unknown mixture. It is a very useful technique for research,forensics,environmental testing, and many more fields because it is simple and inexpensive way to analyze small samples. In this experiment two compounds (solid) were used ferrocene and acetylferrocene. In the first step 50 ml of 2:8 diethyl ether/petroleum ether was placed in an erlenmeyer flask covered with a parafilm paper to avoid evaporation. Then the glass column was prepared placing a small cotton on the bottom of the glass column and then added a small amount of sand , wich will give the stationary phase an even base and prevent concentration and streaking of the bands
Therefore, the gas chromatography could not be performed to determine its composition. The ratio of the three samples obtained, were not all accurate. The first sample, of pure hexane should have had a ratio close to 100% hexane to 0% heptane. The second ratio should have been close to 50% hexane to 50% heptane and the third should have been the reverse of the first sample, with 0% hexane to 100% heptane. The boiling point of hexane is around 65°C and the boiling point of Heptane is 100°C. The first sample’s error could have occurred due to the late extraction of the sample. When the boiling point was reached, the extraction of the sample from the distillation vial should have occurred immediately, not doing so caused some of the vapors from heptane to be included into the first sample. This could be prevented next time by lowering the heat of the Variac transformer, which would have allowed for the heating of the compound to be slower than what it was
The purpose of this experiment was to test for quality control and analysis of a commercial product, in this case vinegar. The experiment performed determined the actual molarity of a specific brand of vinegar as compared to information provided on the bottle. The standardization of HCl and NaOH was also performed in order to understand the process of titrations. The importance of testing for quality control to be sure the product being sold holds up to its commercial value and is authentic in what it advertises to be. Quality control is a way to test the standards of a commercial product by testing a sample of the output against original specifications. Quality control is also used to protect public health and ensure the safety
The combination of the separation technique of LC allows pure compounds to enter the identification by mass spectrometry and therefore increases the chance of successful identification of an unknown substance. This is based on the principle that many compounds with identical retention characteristics have different mass spectra and in this way can be differentiated. The...