4. Any hanging drop was removed from the jet, and the sodium hydroxide was then drawn up using the pipette, to above the graduation mark and allowed to run into the sink. This process was the rinsing of the pipette. 5. Sodium hydroxide was again drawn up using the pipette, to above the graduation mark, where the meniscus was allowed to fall until the bottom of it was rested on the graduation mark when viewed at eye level.
While stirring, 6 M NaOH was added drop-wise until the solution became basic, turning red litmus paper blue. A total of 3.84 mL NaOH was required to achieve this; the resulting solution appearing dark blue with cloudy precipitates. The solution was then heated gently atop a hot plate to catalyze the next reaction, with care taken to assure all residue was kept off the walls of the beaker. Heating continued until the reaction reached completion and the solution slowly changed from blue to a dark green and finally black. At this point the heat was turned off to allow the black solid in the beaker, CuO, to settle to the bottom.
The term Cp is the specific heat of the material (at constant atmospheric pressure). Different materials have different specific heat values. The units of specific heat are : Joules/gram deg – C. In this lab we will find the specific heat value of Zinc and compare it to accepted values.This will do by heating a mass of Zinc up to the temperature of boiling water and placing the hot metal into a cup of cold water. The thermal energy that the zinc loses goes into heating up the water in the cup. By knowing the starting temperatures and the final temperature of the water and the zinc, the specific heat of Zinc may be easily obtained.
5. The burette was then refilled with the NaOH and the meniscus was adjusted so that it sat at 0.0mL 6. The pipette was filled with the acetic acid and then drained once again to ensure the pipette wasn’t contaminated as otherwise the obtained results could have been incorrect. 7. The pipette was then filled with 25.0mL’s of acetic acid and then drained into a conical flask, to speed up the process both of the conical flasks were filled with 25.0mL of the acetic acid.
After all the acid has been completely added and the reaction has stopped, use a pipette to add a few extra drops of acid into the beaker until the reaction stops. 7. Place the beaker on a hot plate and heat on a high setting to boil off the water. WARNING: THERE WILL BE A SMALL AMOUNT OF HYDROCHLORIC ACID BOILING OF THE MIXTURE. DO NOT PLACE YOUR FACE DIRECTLY ABOVE THE BEAKER.
6) The ether was removed using the rotary evaporator. We discarded the used MGSO4 into solid waste containers. The solid that remained after ether evaporated was the neutral organic compound. 7) We scraped the solid from the flask with a spatula and allowed the solid to dry thoroughly on a piece of filter
Mixture is gently swirled and drained out into an Erlenmeyer flask. Anhydrous magnesium sulfate is added to dehydrate the washed mixture. The solution is then filter into a weighed, dry, 100mL Erlenmeyer flask. Dichloromethane in the mixture is vaporized with a rotary evaporator. The Caffeine, white powder residue, (0.0486g) should be obtained.
The paper was then put into a beaker of a hydrochloric acid, ethanol, and butanol mixture, being sure that the paper does not touch the sides of the beaker, and then topped. After the eluting solution has risen to within two centimeters of the top of the filter paper, the paper was removed from the beaker, dried, and was stained with a staining reagent solution containing potassium ferrocyanide and potassium iodide. This reagent forms colored precipitates or reaction products with many cations, including all of those used in this experiment. The distance of which the spots moved were determined by calculating the Rf value of each substance. The Rf value is determined by following formula: Rf=DL=distance component movesdistance solvent moves This experiment was successful overall, given a few errors.
Discussion & Conclusion In this experiment we learned how to synthesize the cyclohexene by dehydration of cyclohexanol. We procedure the first step where we have to mix the components. Then we heat the R.B.F with a fractionating column, distilled water. Then we obtained the layers, and we transferred the organic layer to a small, dry Erlenmeyer flask. We added anhydrous Sodium Sulfate as a drying agent.
Benzophenone Harmful & Irritant Wash spillages away with water Hydrochloric acid Corrosive & Irritant wash spillages away with water. Introduction In this experiment, we will see the reduction of the aromatic ketone benzophenone with sodium borohydride to diphenylmethanol. The reducing agent is used in excess to ensure complete reduction of carbonyl group, and the reaction is carried out in aqueous ethanolic solution. The product is easily isolated, purified by crystalisation. By using TLC and IR spectrum, we will see the difference between benzophenone (starting material) and diphenylmethanol (final product).