Reaction Yield (2 parts) Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (AI(C₂H5)3). 3SnCl4 + 4AI(C₂H5)33Sn(C₂H5)4 + 4AICI3 In one experiment, 0.280 L of SnCl4 (d = 2.226 g/mL) was treated with 0.484 L of triethylaluminum (AI(C₂H5)3); d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C₂H5)4)? 1pts Submit Answer Incorrect. Tries 1/5 Previous Tries If 0.418 L of tetraethylstannane (d = 1.187 g/mL) were actually isolated in this experiment, what was the percent yield? % 1pts Submit Answer Tries 0/5 Copyright: Department of Chemistry, Simon Fraser University - SFU Chemistry 2000-2022 Post Discussion Send Feedback

Reaction Yield (2 parts) Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (AI(C₂H5)3). 3SnCl4 + 4AI(C₂H5)33Sn(C₂H5)4 + 4AICI3 In one experiment, 0.280 L of SnCl4 (d = 2.226 g/mL) was treated with 0.484 L of triethylaluminum (AI(C₂H5)3); d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C₂H5)4)? 1pts Submit Answer Incorrect. Tries 1/5 Previous Tries If 0.418 L of tetraethylstannane (d = 1.187 g/mL) were actually isolated in this experiment, what was the percent yield? % 1pts Submit Answer Tries 0/5 Copyright: Department of Chemistry, Simon Fraser University - SFU Chemistry 2000-2022 Post Discussion Send Feedback

Chemistry: The Molecular Science

5th Edition

ISBN:9781285199047

Author:John W. Moore, Conrad L. Stanitski

Publisher:John W. Moore, Conrad L. Stanitski

Chapter11: Chemical Kinetics: Rates Of Reactions

Section: Chapter Questions

Problem 35QRT: The compound p-methoxybenzonitrile N-oxide, which has the formula CH3OC6H4CNO, reacts with itself to...

See similar textbooks

Similar questions

In which solvent, (CH3)2C=O or [(CH3)3C]2C=O, is NaCl more soluble? Explain.
Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(C2H5)3). 3SnCl4 + 4AI(C2H5)3 →3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.160 L of SnCl4 (d = 2.226 g/mL) was treated with 0.346 L of triethylaluminum (Al(C2H5)3): d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C2H5)4)? If 0.257 L of tetraethylstannane (d= 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?
Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides.One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(C2H5)3). 3SnCl4 + 4Al(C2H5)3 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.230 L of SnCl4 (d = 2.226 g/mL) was treated with 0.396 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). If 0.335 L of tetraethylstannane (d = 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?
Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(CzHs)3). 3SnCl4 + 4Al(C2H5)3 → 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.160 L of SnCl4 (d= 2.226 g/mL) was treated with 0.346 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C2H5)4)? If 0.257L of tetraethylstannane (d= 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?
Organometallic compounds such as magnesium and lithium are characterized by the C-M bond. Explain in detail why these compounds function as bases, which ends up limiting their application to ethereal reaction conditions.
Predict the products of the following reactions: [PtCl4]2- + NO2- → (a) (a) + NH3 → (b) [PtCl3NH3]- + NO2- →(c) (c) + NO2- → (d) [PtCl(NH3)3]+ + NO2- → (e) (e) + NO2- → (f) [PtCl4]2- + I- → (g) (g) + I- → (h) [PtI4]- + Cl- →(i) (i) + Cl- → (j)
FeCl3 or AlCl3 are also generally used as catalysts for Friedel-Crafts alkylations. Why might one start with Al as the catalyst starting point instead?
The compound p-methoxybenzonitrile N-oxide, which has the formula CH3OC6H4CNO, reacts with itself to form a dimer—a molecule that consists of two p-methoxybenzonitrile N-oxide units connected to each other (CH3OC6H4CNO)2. The reaction can be represented as A + A → B or 2 A → B where A represents p-methoxybenzonitrile N-oxide and B represents the dimer, (CH3OC6H4CNO)2. For the reaction in carbon tetrachloride at 40 °C with an initial concentration of 0.011 M, these data were obtained: Determine the rate law for the reaction. Determine the rate constant. Determine the order of the reaction with respect to A.
One of the steps in fat metabolism is the hydration of crotonate to yield 3-hydroxybutyrate. This reaction occurs by addition of â€”OH to the Si face at C3, followed by protonation at C2, also from the Si face. Draw the product of the reaction, showing the stereochemistry of each step.
Provide the systematic name of the following compound: [PtBrC12(py)]-
1)Use the mechanism for the cobalt carbonyl hydride ( (HCo(CO)4 ) catalyzed hydroformylation of 1-hexene to illustrate how hexane can occur as a side product . 2)Outline how Fe(CO)5 can function as a catalyst for the water gas shift reaction ( CO + H2O ⇄ CO2 + H2 ) .
Write structural formulas for the following compounds. (2R,3S)-2-methoxypentan-3-ol (i) trans-2,3-dimethyloxirane