What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this experiment?
Assume that you have collected 0.15g of Triphenylmethanol for the question.
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What is the theoretical yield (in grams) and percent yield of
your triphenylmethanol product in this...
The weight of triphenylmethanol is 0.060g QUESTIONS 1. (4 Points) What is the theoretical yield (in...
The weight of triphenylmethanol is 0.060g
QUESTIONS 1. (4 Points) What is the theoretical yield (in grams) and percent yield of your triphenyl- methanol product in this experiment? EXPERIMENTAL PROCEDURE All glassware used in a Grignard reaction must be scrupulously dried. Dry the following glassware in an oven at 110°C for at least 20 minutes: drying tube, Claisen adapter, 8 mL conical vial, 5 mL conical vial, air condenser, glass stirring rod, and a magnetic spinvane. DO NOT PLACE O-RINGS...
What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this...
What is the theoretical yield (in grams) and percent yield of your
triphenylmethanol product in this experiment? (Weight of
triphenylmethanol: 0.060g)
BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...
I need help finding the theoretical yield (in grams) of triphenyl methanol product in this experiment....
I need help finding the theoretical yield (in grams) of
triphenyl methanol product in this experiment. PLEASE SHOW WORK, I
would like to learn the steps.
below is pictures of the procedure with amounts of chemicals
used
126 Experiment 10 EXPERIMENTAL PROCEDURE All glassware used in a Grignard reaction must be scrupulously dried, Dry the following glasstare in an af 110°C for at last 20 mini drying to Canadair 8 ml comical rial 5 ml con vial, air cond glass...
Grignard Reaction with a Ketone: Triphenylmethanol Introduction: The purpose of this lab is to prepare phenylmagnesium...
Grignard Reaction with a Ketone: Triphenylmethanol Introduction: The purpose of this lab is to prepare phenylmagnesium bromide, a Grignard reagent, and react it with benzophenone to give triphenylmethanol. Grignard reagents are very reactive and must be synthesized in an environment free of water or any other source of potential proton donor. Once made, the Grignard reagent will do a nucleophilic attack on the carbonyl carbon of the ketone, benzophenone. The result is an alkoxide that is then protonated to give...
using pictures and a maximum of 10 words, explain why an oven-dried 5-ml conical vial and...
using pictures and a maximum of 10 words, explain why an oven-dried
5-ml conical vial and drying tube(step 1 and 2 of part 1) are used
in the reaction. do both please! also the notebook pages are the
procedure
(1) Using pictures and a maximum of 10 words, explain why an oven-dried 5-ml conical vial and drying tube (step 1 and 2 of Part 1) are used in the reaction. (2) After the addition of benzophenone to the mixture of...
What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this...
What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this experiment? Assume you have collected 0.15 g of triphenylmethanol. Br 2 Mg Ether MgBr 1) PhCO2CH3 2) HCI 2 2 Ph3COH + CH3OH Figure 10.1. The stoichiometry of a Grignard reaction. Br MgBr 2 1) 2 Mg Ether 2 2) PhCO2CH3 i MgBr OCH3 Ph Ph Ph CH30 + Benzophenone, III II Ph - MgBr OH MgBr 3) HCI Ph Ph Ph Ph Ph...
i need help with post questions, thanks Product Isolation After stirring the reaction for 5 minutes...
i need help with post questions, thanks
Product Isolation After stirring the reaction for 5 minutes and allowing the reaction mixture to cool (the reaction can be exothermic), remove the Claisen head from the conical vial. Slowly add 3 M HCl(aq) drop-wise. The solid may need to be broken up with a stirring rod or a pipet. Continue to add acid until the aqueous phase (bottom layer) tests positive with pH paper. Extractions can be done using the conical funnel...
QUESTIONS TO ANSWER: Prepare a table of all chemicals used with the structure and purpose of...
QUESTIONS TO ANSWER:
Prepare a table of all chemicals used with the structure and
purpose of each.
Calculate the theoretical yield by finding limiting reactant of
the experiment by converting reactants to product (remember to show
all calculations used)
Calculate the percent yield using the limiting reactant
Calculate the Rf for triphenylmethanol. If there are two dots,
determine which one is triphenylmethanol.. ( I did not provide
data. Please let me know how I Would do this if I did)...
Find the crude yield and percent yield of trans-4-methoxycinnamic acid Find the crude and percent yield...
Find the crude yield and percent yield of trans-4-methoxycinnamic
acid
Find the crude and percent yield of ethyl trans-4
methoxycinnamic acid
Synthesis of trans-4-methoxycinnamic acid 0.585 gused To a 25 mL round-bottom flask equipped with a stir bar, add 1 mL of pyridine (Caution! Pyridine is toxic!) followed by 320 mg of 4-methoxybenzaldehyde, 320mg 10. 200ML 585 mg of malonic acid and 33 mg of B-alanine. Clamp the round-bottom flask Ucdi over a stir plate in a sand bath and...
please find the purpse, Discussion, conclusion un 27 Phoenix June 20 8:10 PM a 35AEXPERIMENT 35A...
please find the purpse, Discussion, conclusion
un 27 Phoenix June 20 8:10 PM a 35AEXPERIMENT 35A Triphenylmethanol PROCEDURE ether MgBr+ C-OH + MgBr(OH) OMgBr 0 Addct Addition of Benzophenone While the phenylmagnesium bromide solution is being heated and stirred under reflux, make a solution of 1.09 g benzophenone in 2 mL of anhrudrous ether in a 5-mL conical vial. Cap the vial until the reflux period is over. Once the Grignard reagent is cooled to room temperature, draw some of...
The weight of triphenylmethanol is 0.060g
QUESTIONS 1. (4 Points) What is the theoretical yield (in grams) and percent yield of your triphenyl- methanol product in this experiment? EXPERIMENTAL PROCEDURE All glassware used in a Grignard reaction must be scrupulously dried. Dry the following glassware in an oven at 110°C for at least 20 minutes: drying tube, Claisen adapter, 8 mL conical vial, 5 mL conical vial, air condenser, glass stirring rod, and a magnetic spinvane. DO NOT PLACE O-RINGS...
What is the theoretical yield (in grams) and percent yield of your
triphenylmethanol product in this experiment? (Weight of
triphenylmethanol: 0.060g)
BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...
I need help finding the theoretical yield (in grams) of
triphenyl methanol product in this experiment. PLEASE SHOW WORK, I
would like to learn the steps.
below is pictures of the procedure with amounts of chemicals
used
126 Experiment 10 EXPERIMENTAL PROCEDURE All glassware used in a Grignard reaction must be scrupulously dried, Dry the following glasstare in an af 110°C for at last 20 mini drying to Canadair 8 ml comical rial 5 ml con vial, air cond glass...
using pictures and a maximum of 10 words, explain why an oven-dried
5-ml conical vial and drying tube(step 1 and 2 of part 1) are used
in the reaction. do both please! also the notebook pages are the
procedure
(1) Using pictures and a maximum of 10 words, explain why an oven-dried 5-ml conical vial and drying tube (step 1 and 2 of Part 1) are used in the reaction. (2) After the addition of benzophenone to the mixture of...
What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this experiment? Assume you have collected 0.15 g of triphenylmethanol. Br 2 Mg Ether MgBr 1) PhCO2CH3 2) HCI 2 2 Ph3COH + CH3OH Figure 10.1. The stoichiometry of a Grignard reaction. Br MgBr 2 1) 2 Mg Ether 2 2) PhCO2CH3 i MgBr OCH3 Ph Ph Ph CH30 + Benzophenone, III II Ph - MgBr OH MgBr 3) HCI Ph Ph Ph Ph Ph...
i need help with post questions, thanks
Product Isolation After stirring the reaction for 5 minutes and allowing the reaction mixture to cool (the reaction can be exothermic), remove the Claisen head from the conical vial. Slowly add 3 M HCl(aq) drop-wise. The solid may need to be broken up with a stirring rod or a pipet. Continue to add acid until the aqueous phase (bottom layer) tests positive with pH paper. Extractions can be done using the conical funnel...
QUESTIONS TO ANSWER:
Prepare a table of all chemicals used with the structure and
purpose of each.
Calculate the theoretical yield by finding limiting reactant of
the experiment by converting reactants to product (remember to show
all calculations used)
Calculate the percent yield using the limiting reactant
Calculate the Rf for triphenylmethanol. If there are two dots,
determine which one is triphenylmethanol.. ( I did not provide
data. Please let me know how I Would do this if I did)...
Find the crude yield and percent yield of trans-4-methoxycinnamic
acid
Find the crude and percent yield of ethyl trans-4
methoxycinnamic acid
Synthesis of trans-4-methoxycinnamic acid 0.585 gused To a 25 mL round-bottom flask equipped with a stir bar, add 1 mL of pyridine (Caution! Pyridine is toxic!) followed by 320 mg of 4-methoxybenzaldehyde, 320mg 10. 200ML 585 mg of malonic acid and 33 mg of B-alanine. Clamp the round-bottom flask Ucdi over a stir plate in a sand bath and...
please find the purpse, Discussion, conclusion
un 27 Phoenix June 20 8:10 PM a 35AEXPERIMENT 35A Triphenylmethanol PROCEDURE ether MgBr+ C-OH + MgBr(OH) OMgBr 0 Addct Addition of Benzophenone While the phenylmagnesium bromide solution is being heated and stirred under reflux, make a solution of 1.09 g benzophenone in 2 mL of anhrudrous ether in a 5-mL conical vial. Cap the vial until the reflux period is over. Once the Grignard reagent is cooled to room temperature, draw some of...
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