We concluded that the rate of hydrolysis of (CH3)3CCl is directly proportional to water content in the solvent mixture. Aims of experiment • Determine the rate constants for hydrolysis of (CH3)3CCl in solvent mixtures of different composition (50/50 V/V isopropanol/water and 40/60 V/V isopropanol/water) • Examine the effect of solvent mixture composition on the rate of hydrolysis of (CH3)3CCl Introduction With t-butyl chloride, (CH3)3CCl, being a tertiary halogenoalkane, it is predicted that (CH3)3CCl reacts with water in a nucleophilic substitution reaction (SN1 mechanism), where Step 1 is the rate-determining step. The reaction proceeds in a manner as shown
One of the reactions you observed resulted in this product: NaCl + H2O + CO2 (g)? What well did this reaction occur in? Describe how the observations for this reaction support your answer. B BoldI ItalicsU Underline Bulleted list Numbered list Superscript Subscript70 Words A reaction I observed in number 1.) Sodium Bicarbonate mixed with Hydrochloric acid.
The graph presents the trend of the rate of reaction decreasing when the temperature is lower. This is shown through the average rate of reaction time being 89.5 seconds for the cold water, while in the hot water the tablet’s average reaction time was 41 seconds. Based on the graph, you can see a significant change between the two times, the average cold water time’s bar have a vast change from the average hot water time’s bar. The reason I chose a bar graph to display my data was to be able to compare distinct categories in an organized manner, while having the changes between them
The goal of the experiment is to synthesize a bromohexane compound from 1-hexene and HBr(aq) under reflux conditions and use the silver nitrate and sodium iodide tests to determine if the product is a primary or secondary hydrocarbon. The heterogeneous reaction mixture contains 1-hexene, 48% HBr(aq), and tetrabutylammonium bromide and was heated to under reflux conditions. Heating under reflux means that the reaction mixture is heated at its boiling point so that the reaction can proceed at a faster rate. The attached reflux condenser allows volatile substances to return to the reaction flask so that no material is lost. Since alkenes are immiscible with concentrated HBr, tetrabutylammonium bromide is used as a phase-transfer catalyst.
The chemical equation for this experiment is hydrochloric acid + sodium thiosulphate + deionised water (ranging from 25ml to 0ml in 5ml intervals) sodium chloride + deionised water (ranging from 25ml to 0ml in 5ml intervals) + sulphur dioxide + sulphur. As a scientific equation, this would be written out as, NA2S2O3 + 2HCL + H2O (ranging from 25ml to 0ml in
To calculate the percentage of Cu, we divided the final mass of the penny 0.09 and the initial mass of 2.47 and multiplied by 100. To calculate the percentage of Zn, we divided the final mass of the penny 2.38 and the initial mass of 2.47 and multiplied by 100. During the experiment the hydrochloric acid donated its hydrogen ions in the reaction and then the chloride ions reacted with the zinc ions in the solution. Thus, the zinc dissolved in the highly acidic solution which was caused by the high concentration of H2 ions. Hydrogen gas was generated during the reaction which was seen when bubbles were formed as the penny was dissolved into the beaker.
Shayna Salloway AP Chemistry A Snyder 11 September 2014 Title: Finding Mole Ratios of Reactants in a Chemical Reaction Purpose: Experiment using the method of continuous variations to figure out mole ratios of reactants. Procedure: 1. Take the NaClO and the sodium thiosulfate solutions and measure the temperature of each solution. Record in the data table. 2.
Purpose: The purpose of this lab is to titrate an unknown solid acid (KH2PO4) with a standardized sodium hydroxide solution. After recording and plotting the data, the acid’s equivalence point will be recorded once the color changes. Using the equivalence point, the halfway point will be calculated, which is used to determine the acid’s equilibrium constant. The acid’s calculated equilibrium constant will be compared with the acid’s established pKa value. Eventually using the NaOH and the acid’s consumed moles, the equivalent mass will be determined.
Hydrolysis Rates of Esters Purpose Esters can be hydrolyzed to the corresponding carboxylic acid and alcohol with a decrease in the pH level as the acidic component is formed. The purpose of this experiment is to compare the hydrolysis rates of esters by monitoring the pH values of their aqueous solutions as a function of time. The esters being compared are ethyl acetate, ethyl benzoate, ethyl formate, and ethyl butanoate while the pH level can be determined by the change in color of the solution with the use of sodium hydroxide (NaOH) for the base and the universal pH indicator. The two factors that affect the rates for the hydrolysis of esters is the steric factor and the electronic factor which will serve as the determining factor of how
The products in both methods were used for recrystallization and TLC. For recrystallization, boiling ethanol was used as the solvent. In the TLC procedure, 90/10 hexane and ethyl acetate was used. NMR was collected for products used in these methods. In this experiment, method 1 generate a mixture of yellowish crystals and a yellowish gluey product.
As seen in the trend of both buffer, once the pH is lower than 3, the slope of dv/dpH increase drastically, showing the decreasing effects of the buffer. On the other hand, in the trend of both buffer on the right side of graph shows when NaOH is added, the change in pH is more drastic once past about pH 5. Although buffer 1 and buffer 2 shows a similar trend, the plot of buffer 1 is above the plot of buffer 2. The reason for this is that buffer 1 is made by an acid and base with an almost equal concentration. This makes buffer 1 a greater buffer compared to buffer 2.
Methodology: The distillation column was analyzed theoretically using McCabe Thiele to establish the number of stages required for separation. The vapor-liquid equilibrium (VLE) data for methanol and 2-propanol was used to plot curves of methanol-vapor fraction versus methanol-liquid fraction, and methanol liquid-vapor fraction versus temperature. III. Results: From the results, the average efficiency was 0.4308, 0.3778, and 0.4956 at 0.57kW supplied (30.58 mL/min Feed; 26.30 mL/min Boil Up), 0.94kW (30.58 mL/min Feed; 52.96 mL/min Boil Up), and 1.27kW (30.58 mL/min Feed; 77.50 mL/min Boil Up) respectively. From the experiment, it was observed that the quality
The topic of research is, “how fast does an Alka-Seltzer tablet make gas?”. In the experiment, the scientists will be measuring the chemical reaction rates that occur, when 1 Alka-Seltzer tablet is placed in a specific temperature of water. The independent variable during the experiment will be the temperature of the water (degrees Celsius). The dependent variable during the experiment will be, the rate in which gas is produced (in seconds). The constants of the experiment, will be the amount of water used and the Alka Selter compound.
The objective of this experiment was to use an aldol condensation reaction to synthesize 3-nitrochalcone from 3- nitrobenzaldehyde. This was accomplished with a Diels-Alder reaction that utilized 3-nitrobenzaldehyde, acetophenone, ethanol, and sodium hydroxide. The mechanism for the synthesis of 3-nitrochalcone is presented in Figures 1 and 2. The alpha carbon on the acetophenone is deprotonated. This is followed by the attack of the alpha carbon anion on the carbonyl carbon on the 3-nitrobenzaldehyde.