After purification, this reaction yielded 5.6 g of product Question #20: Using the mmoles of benzene calculated e...
After mixing for three hours, the product is extracted into Dichloromethane and the solvent is removed to give 5.5 g of a yellow oil. Question #31: Using the mmoles of nitrobenzene calculated earlier (45.5) and the molecular weight of the product (157.5 g/mol) predict the theoretical 100% yield of the product in grams. Round to the hundredths place. Question #32: Using this number predict the experimental yield (reminder, the reaction produced 5.5 g of product.) Round to the nearest whole...
Question #15: Using the molecular weight (130 g/mol) of methyl (S)-2-methyl-4-oxobutanoate calculated earlier (3.8) and the molecular weight of the product (188 g/mol) predict the theoretical 100% yield of the product in milligrams. Round to the tenths place. mg
As indicated early, the next step of our synthesis will be a Chlorination reaction. Just like before we need to calculate the amount of nitrobenzene we will need. Remember, we obtained 5.6 g of this in the first step. Question #23: Using the molecular weight (123 g/mol) determine the amount of mmol of nitrobenzene. Round to the tenths place. mmol For this reaction to occur, you will need at least one molar equivalents of Cl2 for each molecule of nitrobenzene....
Question text A limiting reagent is Choose...consumed completelyleft over in excess during a chemical reaction, and it Choose...decreasesincreases the possible amount of product that can be formed. Question 2 Not yet answered Points out of 1 Flag question Question text A student used 7.15 g of CaCl2 and 9.25 g of K2CO3 to make CaCO3. The reaction is: K2CO3(aq) + CaCl2(aq) = CaCO3(s) + 2KCl(aq). Based on the masses of the two reactants given, the limiting reagent is Choose...CaCl2K2CO3 ....
I did an experiment where I synthesized 2-phenyl-2-propanol using the grignard reaction. please help me answer these lab questions Reagents Moles of Reagent 0.00142 moles (0.224 g)bromobenzene 0.00712 mol (0.173 g) 2 mL of THF (n/a moles) tetrahydrofuran 0.00142 mol (0.083g, 0.11mL) acetone, HPLC grade, anh Reagent Name FW 157.75 24.31 n/a 58 Comments Mg powder grind before using must be anhydrous must be anhydrous Pre-Lab Assignment: 1. Determine the volume (mL) of bromobenzene needed for the experiment. Obtain the...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the experimental section above) H2SO4 + Na2Cr207 2H20- H2O, A Molecular Weight Theoretical yield amount moles on (if applicable) Equivalents 2. Look up the melting point for p-nitrobenzoic acid and record the reference. 3. What color change is expected to be observed in the reaction? Explain why. CHROMIC ACID OXIDATION Experimental Procedure: Part I: Synthesis of p-nitrobenzoic Acid 1. Under the hood, add 0.400 g...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...
please help answer question 4, a-f please using the data below from chart 1 objectives from lab, thank you DATA:CA y 3 Ay No3 Part I: Cell Potential of voltaic cells under standard conditions: cell CU CND2 #27 14.0m Give the half Half cell reaction at Combinations Oxidation Reduction E the anode and with [ion] takes place Theoretical takes place cathode. Write in M here here (V) above the arrow E c (V) if it is oxidation or reduction. |-0.340...