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1. (6 pts) Provide two different syntheses for 1,1-diphenyl-1-butanol starting from a carbonyl compound and using a...
III. Grignard Reagents. 1. (6 pts) Provide two different syntheses for 1,1-diphenyl-1-butanol starting from a carbonyl...
III. Grignard Reagents. 1. (6 pts) Provide two different syntheses for 1,1-diphenyl-1-butanol starting from a carbonyl compound and using a Grignard reagent. Synthetic Route 1: carbonyl Grignard reagent a) THE b) H3O+ work up OH 1,1-diphenyl-1-butanol Synthetic Route 2: carbonyl Grignard reagent a) THE b) H3O+ work up 1,1-diphenyl-1-butanol
2. (3 pts) The use of Grignard reagents requires scrupulously dry aprótic solvents such as diethyl...
2. (3 pts) The use of Grignard reagents requires scrupulously dry aprótic solvents such as diethyl ether or tetrahydrofuran. Please explain why the solvents need to be scrupulously dry. To support your reason, show the reaction that occurs if the solvent is wet.
help with 23 HAPTER 14: ORGANOMETALLIC COMPOUNDS TWO common solvents for Grignard reagents are: 1) ethanol...
help with 23
HAPTER 14: ORGANOMETALLIC COMPOUNDS TWO common solvents for Grignard reagents are: 1) ethanol and diethyl ether. 2) diethyl ether and tetrahydrofuran (THF). 3) tetrahydrofuran (THF) and toluene. 4) water and ethanol. What is the product of the following reaction? CH, CH. CHCH.CH - ether 2) 2-ethyl-1-pentanol 2) 2-ethyl-1-butanol 3) 3-pentanel 4) 3-aethyl-1-pentanc: The reaction of benzyl sagnesius bromide (C.HSCHMB) with acetaldehyde (CHC40) followed by hydrolysis yields: 1) 1-phenyl-1-propanol 2) 1-phenyl-2-propanol 3) 2-phenyl-2-propanel 4 .-ghen -propane: mo synthesize...
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepa...
i need help with the prelab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
Organic chemistry post-lab question: "Why is important to add the alkyl halide dropwise in your reaction?...
Organic chemistry post-lab question: "Why is important
to add the alkyl halide dropwise in your reaction? (Hint: your
reaction is not heated, but you still need a water-cooled
condenser!)" Please answer in detail!
Here is a copy of the experiment, thank you!
The Grignard reaction is an important synthetic process by which a carbon-carbon bond is formed. Magnesium metal is first reacted with an organic halide. The resultant organo-magnesium halide (Grignard reagent) is then combined with a carbonyl compound, ultimately...
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepa...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
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)bromoben...
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...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
Total Points:/36 Section 1: Multiple Choice (6 pts) AIkyl halides can be converted into Grignard reagents...
Total Points:/36 Section 1: Multiple Choice (6 pts) AIkyl halides can be converted into Grignard reagents by which of the following methods? 1. a. Retluxing alky I halide and adding Mg metal in Alcohol solution. b. Reluxing with MgC solution c. Warming solution and adding Mg powder in dry Diethyl Ether. d. A and C, but not B. 2. In the Nylon experiment, why was NaOH added to the aqueous layer? Catalyze reaction Increase reaction rate Neutralize HCl as it...
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...
III. Grignard Reagents. 1. (6 pts) Provide two different syntheses for 1,1-diphenyl-1-butanol starting from a carbonyl compound and using a Grignard reagent. Synthetic Route 1: carbonyl Grignard reagent a) THE b) H3O+ work up OH 1,1-diphenyl-1-butanol Synthetic Route 2: carbonyl Grignard reagent a) THE b) H3O+ work up 1,1-diphenyl-1-butanol
2. (3 pts) The use of Grignard reagents requires scrupulously dry aprótic solvents such as diethyl ether or tetrahydrofuran. Please explain why the solvents need to be scrupulously dry. To support your reason, show the reaction that occurs if the solvent is wet.
help with 23
HAPTER 14: ORGANOMETALLIC COMPOUNDS TWO common solvents for Grignard reagents are: 1) ethanol and diethyl ether. 2) diethyl ether and tetrahydrofuran (THF). 3) tetrahydrofuran (THF) and toluene. 4) water and ethanol. What is the product of the following reaction? CH, CH. CHCH.CH - ether 2) 2-ethyl-1-pentanol 2) 2-ethyl-1-butanol 3) 3-pentanel 4) 3-aethyl-1-pentanc: The reaction of benzyl sagnesius bromide (C.HSCHMB) with acetaldehyde (CHC40) followed by hydrolysis yields: 1) 1-phenyl-1-propanol 2) 1-phenyl-2-propanol 3) 2-phenyl-2-propanel 4 .-ghen -propane: mo synthesize...
i need help with the prelab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
Organic chemistry post-lab question: "Why is important
to add the alkyl halide dropwise in your reaction? (Hint: your
reaction is not heated, but you still need a water-cooled
condenser!)" Please answer in detail!
Here is a copy of the experiment, thank you!
The Grignard reaction is an important synthetic process by which a carbon-carbon bond is formed. Magnesium metal is first reacted with an organic halide. The resultant organo-magnesium halide (Grignard reagent) is then combined with a carbonyl compound, ultimately...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
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...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
Total Points:/36 Section 1: Multiple Choice (6 pts) AIkyl halides can be converted into Grignard reagents by which of the following methods? 1. a. Retluxing alky I halide and adding Mg metal in Alcohol solution. b. Reluxing with MgC solution c. Warming solution and adding Mg powder in dry Diethyl Ether. d. A and C, but not B. 2. In the Nylon experiment, why was NaOH added to the aqueous layer? Catalyze reaction Increase reaction rate Neutralize HCl as it...
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...
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