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1) Write a stepwise mechanisms for the bromination of: a) trans-stilbene and b) cis-stilbene (substitute benzene...
help with limiting reagents and percent yield needed the reactions are the bromination of cis-stilbene and...
help with limiting reagents and percent yield needed
the
reactions are the bromination of cis-stilbene and trans-stilbene.
The reagents and the moles of each reagent are in my data, as is
the moles of the products formed. The volume and mass of the
reagents are given as well. I need to know how to find the percent
yield and what the limiting reagents are for both the trans and cis
stilbene brominations. The information is there.
Name Physical Properties of...
So we are doing a Green Bromination of Stilbene and need to calculate the percent yield...
So we are doing a Green Bromination of Stilbene and need to calculate the percent yield of the reaction Percent yield of 1,2-dibromo-1,2-diphenylethane the starting material: molecular weight =66g/mol starting mass = 1.28 g the product molecular weight= 164 g/mol At the completion of your reaction you isolated 2.61 g of your desired product. From the following information calculate the % yield of your reaction. Show your work and watch sigfigs!
number 5 please EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute first step of...
number
5 please
EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute first step of two-step sequence to transform an alkene into an alkyne via a dihalide intermediate and use infrared spectroscopy to identify functional groups 5. Identify the limiting reagent for the reaction and explain why it is the limiting reagent. PLEASE NOTE: You will need to draw out a Table of Reagents in your notebook to ensure that you know how many moles of each reagent you...
here is the procedure if needed EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute...
here is the procedure if needed
EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute first step of two-step sequence to transform an alkene into an alkyne via a dihalide intermediate and use infrared spectroscopy to identify functional groups PRELAB NOTEBOOK: In the laboratory notebook, write the overall experimental objective, chemical equation(s), reaction mechanism (consider all possible stereoisomers), draw a diagram or outline of the procedural steps, and complete the chemical safety table for all chemicals. 1. Why is...
number 5 please EXPERIMENT 8: BROMINATION OF TRANS-STILBENE Br3 Br glacial acetic acid Br Objective: Execute...
number
5 please
EXPERIMENT 8: BROMINATION OF TRANS-STILBENE Br3 Br glacial acetic acid Br Objective: Execute first step of two-step sequence to transform an alkene into an alkyne via a dihalide intermediate and use infrared spectros copy to identify functional groups 5. Identify the limiting reagent for the reaction and explain why it is the limiting reagent. PLEASE NOTE: You will need to draw out a Table of Reagents in your notebook to ensure that you know how many moles...
Bromination of Alkenes 1: Write the reaction for the transformation of trans-stilbene to products, and why...
Bromination of Alkenes 1: Write the reaction for the transformation of trans-stilbene to products, and why do we not see carbocation in this reaction? Pyridinium Tribromide was used instead Elemental Bromine and Ethanol was used as a solvent Also, what would be the limiting reagent in this reaction and why?
1. Most of the class will be brominating trans-stilbene (part B) and the rest cis-stilbene (part...
1. Most of the class will be brominating trans-stilbene (part B) and the rest cis-stilbene (part A). For this assignment write a detailed procedure in your lab notebook for Part B. Upload a picture/scanned copy (5 pts). Tip: If you write the procedure down the left half of the page, you can leave space to record your measurements/observations down the right side of the page. If you end up using cis-stilbene in the experimental there will only be a few...
In H.O. House's Prilezhaev epoxidation of trans-stilbene, the stereospecific organic reaction product would be named 33....
In H.O. House's Prilezhaev epoxidation of trans-stilbene, the stereospecific organic reaction product would be named 33. coH CPBA in CH Cy/+20 C/15 h NaOAc (bufler) os v aso (78-83s% yield) (al (E)-2,3-diphenyloxirane Ic] trans-stillbene oxide bl (E)-1,2-epoxy-1,2-diphenylethane (d] (2)-2,3-diphenyloxirane 34. Draw the major organic product(s) for the following reactions; (") must include correct stereochemistry, double-dagger (#) must show le) A, B&C two products HBr (a) нвr (b) (1.00 equiv) наг (c) HCI (d) 48% wt. HBr (e) 37% wt. HCI...
The theoretical yield of 1,2-epoxycyclohexane is _grams, when starting with 3.0 grams of trans-2- bromocyclohexanol. (Enter...
The theoretical yield of 1,2-epoxycyclohexane is _grams, when starting with 3.0 grams of trans-2- bromocyclohexanol. (Enter the number using 3 significant figures, i.e. 1.22) Given: 3.0 g of trans-2-bromocyclohexanol FW: 179.05 25 mL of 10% NaOH FW: 40 and density: 1.11 g/mL 1,2-expoxycyclohexane FW: 98.15 Hint: Identify the limiting reactant (NaOH or trans-2- bromocyclohexanol) by calculating the number of moles of each. For 1 mole of limiting reactant, 1 mole of product is formed. Use the # of moles and...
1. (27 pts) Shown below is the condensation of 4-methylbenzene-1,2-diamine and 4- methyl-pentanoic acid. The amounts of each starting material used in the reaction are given. Also, the amount of...
1. (27 pts) Shown below is the condensation of 4-methylbenzene-1,2-diamine and 4- methyl-pentanoic acid. The amounts of each starting material used in the reaction are given. Also, the amount of product obtained from the reaction is indicated Please answer each of the following questions. Show all of your work in order to obtain full credit NH2 intmdt + H2O но NH2 5-Methyl-2-(3-methyl-buty)- 1H-benzoimidazole 4-methyl- pentanoic acid C$H1202 Mol. WI: 116 2 density 0.92 g/ml ene- 1.2-diamine C13H18N2 Mol. Wt.: 202.3...
help with limiting reagents and percent yield needed
the
reactions are the bromination of cis-stilbene and trans-stilbene.
The reagents and the moles of each reagent are in my data, as is
the moles of the products formed. The volume and mass of the
reagents are given as well. I need to know how to find the percent
yield and what the limiting reagents are for both the trans and cis
stilbene brominations. The information is there.
Name Physical Properties of...
number
5 please
EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute first step of two-step sequence to transform an alkene into an alkyne via a dihalide intermediate and use infrared spectroscopy to identify functional groups 5. Identify the limiting reagent for the reaction and explain why it is the limiting reagent. PLEASE NOTE: You will need to draw out a Table of Reagents in your notebook to ensure that you know how many moles of each reagent you...
here is the procedure if needed
EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute first step of two-step sequence to transform an alkene into an alkyne via a dihalide intermediate and use infrared spectroscopy to identify functional groups PRELAB NOTEBOOK: In the laboratory notebook, write the overall experimental objective, chemical equation(s), reaction mechanism (consider all possible stereoisomers), draw a diagram or outline of the procedural steps, and complete the chemical safety table for all chemicals. 1. Why is...
number
5 please
EXPERIMENT 8: BROMINATION OF TRANS-STILBENE Br3 Br glacial acetic acid Br Objective: Execute first step of two-step sequence to transform an alkene into an alkyne via a dihalide intermediate and use infrared spectros copy to identify functional groups 5. Identify the limiting reagent for the reaction and explain why it is the limiting reagent. PLEASE NOTE: You will need to draw out a Table of Reagents in your notebook to ensure that you know how many moles...
1. Most of the class will be brominating trans-stilbene (part B) and the rest cis-stilbene (part A). For this assignment write a detailed procedure in your lab notebook for Part B. Upload a picture/scanned copy (5 pts). Tip: If you write the procedure down the left half of the page, you can leave space to record your measurements/observations down the right side of the page. If you end up using cis-stilbene in the experimental there will only be a few...
In H.O. House's Prilezhaev epoxidation of trans-stilbene, the stereospecific organic reaction product would be named 33. coH CPBA in CH Cy/+20 C/15 h NaOAc (bufler) os v aso (78-83s% yield) (al (E)-2,3-diphenyloxirane Ic] trans-stillbene oxide bl (E)-1,2-epoxy-1,2-diphenylethane (d] (2)-2,3-diphenyloxirane 34. Draw the major organic product(s) for the following reactions; (") must include correct stereochemistry, double-dagger (#) must show le) A, B&C two products HBr (a) нвr (b) (1.00 equiv) наг (c) HCI (d) 48% wt. HBr (e) 37% wt. HCI...
The theoretical yield of 1,2-epoxycyclohexane is _grams, when starting with 3.0 grams of trans-2- bromocyclohexanol. (Enter the number using 3 significant figures, i.e. 1.22) Given: 3.0 g of trans-2-bromocyclohexanol FW: 179.05 25 mL of 10% NaOH FW: 40 and density: 1.11 g/mL 1,2-expoxycyclohexane FW: 98.15 Hint: Identify the limiting reactant (NaOH or trans-2- bromocyclohexanol) by calculating the number of moles of each. For 1 mole of limiting reactant, 1 mole of product is formed. Use the # of moles and...
1. (27 pts) Shown below is the condensation of 4-methylbenzene-1,2-diamine and 4- methyl-pentanoic acid. The amounts of each starting material used in the reaction are given. Also, the amount of product obtained from the reaction is indicated Please answer each of the following questions. Show all of your work in order to obtain full credit NH2 intmdt + H2O но NH2 5-Methyl-2-(3-methyl-buty)- 1H-benzoimidazole 4-methyl- pentanoic acid C$H1202 Mol. WI: 116 2 density 0.92 g/ml ene- 1.2-diamine C13H18N2 Mol. Wt.: 202.3...
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