Fractional Distillations Essay Example for Free

Fractional Distillations EssayIn this experiment we aim to read that we can separate two volatile compounds from a mixture due(p) to the different chemical properties of each compound. We will accomplish this by a separation procedure known as distillation, which relies on each compound having a distinct and separate boiling level. Our pure products will be analyzed with gas chromatography to determine the success of the distillation. ProceduresThe experiment was performed as stated in the way textbook Pavia, D. L., Lampman, G. M., Kriz, G. S., Engel, R. G. Introduction to Organic Laboratory Techniques A Microscale Approach. 2007, 4th Ed. Pp 5157. . DataThe distillation curves for our open and fractional distillation (See page 3) clearly demonstrate that fractional distillation separates the two compounds more completely. The boiling point (bp) of our unknown compounds was taken from the flat regions of the fractional distillation curve. Our unknown mixture contained hexane (bp 69 C) and toluene (bp 110.6 C). Analysis via gas chromatography allowed us to determine the relative percentage of hexane and toluene at fractions near the beginning and end of our distillations. Relative percentages need been recorded in the table below, and our calculations are shown on page 5.ConclusionThis week we utilized two methods of distillation (simple and fractional) to separate a mixture of two volatile compounds. We institute that while the simple distillation separated the majority of the two compounds near the beginning and the end of the distilling process, fractional distillation produced much more pure fractions. In simple distillation the column was shorter, allowing less room for the two different compounds to fully separate. While heating the round-bottom flask the hexane molecules gain higher energizing energy faster than the toluene molecules due to their lower molecular weight and lesser intermolecular forces. The longer fractionaldistillation column allowed the hexane molecules with higher kinetic energy to separate from the lower-energy toluene molecules.After viewing the gas chromatograph data from the fractional distillation we saw that our unknown compounds had almost completely separated, while the fractions from the simple distillation were less pure. Although distillation is a good separation technique it is still necessary to ensure that proper steps are taken to descend the chances of error. Failure to add a boiling chip to the round-bottom flask could allow the mixture to heat unevenly. This could allow molecules with a higher boiling point to gain kinetic energy before the molecules with the lower boiling point, which would create impure fractions. Watching the rate of temperature increase is also important. Allowing the temperature to increase too quick can cause impurity for the same reason.We forgot to add the boiling chip to the round-bottom flask in the simple distillation, which could stir contributed to th e mixture of toluene and hexane that we saw. We make sure to include the boiling chip in the fractional distillation, however, and did not observe any problems. Even though both hexane and toluene are volatile, they have different chemical properties to allow for separation and analysis. Hexane is a hydrocarbon with no dipole moment or double bonds. This means that it has few intermolecular interactions, and will have a lower boiling point. It also has a lower molecular weight than toluene, so it will appear first on the gas chromatograph.methylbenzene has a benzene ring with a methyl group attached. Toluene has greater intermolecular forces than hexane because the benzene ring withdraws electrons from the methyl group. This creates a slight signboard to the molecule that increases intermolecular forces and increases the boiling point. Since toluene has a greater molecular weight than hexane it will appear second on the gas chromatograph. This experiment illustrates how multipurpo se the different properties of compounds can be while trying to purify mixtures of compounds.