In the fourth step, the molecule undergoes deprotonation with the help of the concentrated sulfuric acid to form isopentyl acetate. The reaction that was carried out in the experiment was a reversible reaction. In order to obtain as much isopentyl acetate as possible, Le Chatelier’s principle was used to ensure that we were able to collect a sufficient amount of isopentyl acetate. Le Chatelier’s principle says that if you disturb a system in equilibrium the equilibrium will shift in order to account for the disturbance. In our experiment, we used excess acetic acid.
Hence, a calcium chloride and cotton were filled inside a drying tube. The condenser was wrapped with parafilm and a paper towel to avoid moistures from entering. The reagent will act as nucleophilic addition to acetone and work up with hydrochloride acid to synthesize 2-methylhexanol. Throughout this process, the solution turns dark grey and develop white precipitates.
TLC was used to identify the actual unknown product as well as other products/reactants present in the filtered solution. The procedure was conducted by placing a TLC plate in a developing chamber that is filled with a small amount of solvent. The solvent cannot be too polar because it will cause spotted compounds on the TLC plate to rise up too fast, while a very non-polar solvent will not allow the spots to move. The polarity of the spots also determines how far it moves on the plate; non-polar spots are higher than polar ones. After spots on the TLC form, the Rf values are calculated and used to analyze the similarity of the compounds.
The purpose of this experiment is to perform a two step reductive amination using o-vanillin with p-toluidine to synthesize an imine derivative. In this experiment, 0.386 g of o-vanillin and 0.276 g of p-toluidine were mixed into an Erlenmeyer flask. The o-vanillin turned from a green powder to orange layer as it mixed with p-toludine, which was originally a white solid. Ethanol was added as a solvent for this reaction. Sodium borohydride was added in slow portion as the reducing agent, dissolving the precipitate into a yellowish lime solution.
In order to determine the value of X, the hydrate is heated on a burner to undergo decomposition reaction to be decomposed into CuSO4 and water vapor. Water vapor is evaporated during the reaction, leaving CuSO4 crystals, which is supposed to be white, in remain. By weighing the mass of CuSO4 and the mass difference of substance before and after the reaction, the mole of CuSO4 and H2O can be calculated. The value of X can thus be determined by calculating the mole ratio of CuSO4 and H2O. In the lab, through calculation, the value of X is determined to equal to 5.361211229, which is close to 5.
We isolated our crude yield while comparing 2 purification techniques: column chromatography and recrystallization. TLC, NMR, and IR spectroscopy were used throughout the process to identify ferrocene and acetylferrocene in addition to evaluating the levels of purity. Evidence: The objective of our experiments was to prepare acetylferrocene from ferrocene. The overall reaction was carried out using 6.1 equivalents of liquid acetic anhydride to 1.8 equivalents of phosphoric acid and concluded with an aqueous workup with NaOH.
Because it is a tertiary benzylic halide, the reaction is considered an SN1 type. To test the purity, the class then uses a TLC. When one places,” a spot of the substance on the absorbent surface of the TLC plate, the solvent (or solvents) run up through the absorbent,” (Zubrick223). The initial mass of the reactant, triphenylmethyl chloride was 2.006 grams. The experiment yield is 1.589g, which is a 80.3% yield.
the output gases travels to the scrubber where they are cooled down by spraying distilled water from the top of the column , so the gases rise up due to its light density . By a help of a fan the gases are pulled from the scrubber to the absorber . there is a chemical in the absorber called as monoethanolamine it has a liquid nature. This chemical is used to absorb CO_2 only and according the high density of it it settled down while other gases goes out. The settled mixture at the bottom can be called as rich miya.