3) Please draw the mechanism for the following reaction: ΗΝΟ, H2SO4 4) Please calculate the theoretical yield of p-...
Calculate the theoretical yield for p-nitroacetanilide (assume that all of the acetanilide would react to form p-nitroacetanilide). (for Electrophilic Aromatic Substitution: Preparation of p-Nitroacetanilide experiment). The weight of acetanilide is 1.0 g.
Draw an arrow pushing mechanism and find the theoretical yield for the Grignard reaction below using the following amounts of reagent with the given molecular weights: 565 microliters of 2-bromopropane (molecular weight = 123g/mol) 304 microliters of 4-methoxybenzaldehyde (molecular weight = 136.15g/mol) molecular weight of product = 180.27g/mol The limiting reagent is _____________. In this experiment, you will prepare the Grignard reagent isopropyl-magnesium bromide from 2-bromopropane. You will allow this Grignard reagent to react with 4-methoxy-benzaldehyde to form a secondary...
3. Draw the complete mechanism of this reaction. (10 pts) Ново H2SO4 4. Draw all possible products for the following reaction. (10 pts) H2O heat Circle your final answers; only circled structures will be graded!
Please draw the arrow pushing mechanism for the following reaction NO2 HNO3 + H2SO4
Calculate the theoretical yield for the following: 1: C8H8O2 + HNO3 ---(H2SO4)---> C8H7NO4 + H2O - pump 7.5mL H2SO4 (18M) into flask - pump 2.5mL H2SO4 (18M) and 1.75mL HNO3 (16M) into separate flask - pour 2.1mL C8H8O2 (density = 1.09g/mL) into first flask with 7.5mL H2SO4 - Transfer H2SO4/HNO3 mixture into flash dropwise over 2-5 minutes
Draw a stepwise mechanism for the following reaction: OH H2SO4 Part 1 out of 3 O HO HSO4 H30 finish structure ... draw structure... H2SO4
Post-Lab Questions for "4Methylcyclohexene Experiment 1. Write a step-wise, arrow.pushing mechanism for the reaction. H2SO4 (aq,conc., 6 drops) HYPO, (0.4 mL) dropel. Q . Ho 2. While the reaction in the lab text gives the product 4-methylcyclohexene, it is possible that several products are formed in this reaction, including 1-methylcyclohexene, because of 1,2-hydride shifts in the carbo-cation intermediate. Show a step-wise, arrow.pushing mechanism for the formation of 1-methylcyclohexene. 1-methylcyclohexene 3. Be sure to calculate an overall percent yield of methylcyclohexenes...
65. Draw the product of the following dehydration reaction. H2SO4 OH Ans: 68. Draw the mechanism for the following dehydration. LOH H2SO4 Ans: 71. Draw an energy diagram for the following reaction, assuming that it is exothermic. OH H2SO4 Ans: 73. What are the steps of arrow pushing involved in the following mechanism? ОН H2SO4 Ans:
Given the amounts of reactants, please calculate the theoretical yield of the expected alkene reaction product, in mL. Do not factor the sulfuric acid into your calculations. Your final answer must appear in the box provided, or it will not be counted. 4-methylcyclohexanol ------H2SO4(aq) -----> 4-methylcyclohexene Molecular Weight (grams/mole) 114.2 g/mol 98.08 g/mol 96.2 g/mol density (grams/mL) 0.914 g/mL 0.799 g/mL volume (mL) 28.0 mL mass (grams) moles Theoretical yield in mL=
4. Calculate the theoretical yield of product in the nitration of methyl benzoate if the reaction was begun with 0.400 g of methyl benzoate. (Show ALL work please.)