Homework Answers
based on the reaction conditions and the possible
reagents and the intermediates and the products are as
follows
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6. (8 points) Starting from bromobenzene, provide a short synthesis of methylbenzoate. 7. (8 points) Give...
Give practical synthesis for benzylbenzoate, and anti-parisitic insecticide, starting from bromobenzene, benzaldehyde and any other reagents...
Give practical synthesis for benzylbenzoate, and anti-parisitic insecticide, starting from bromobenzene, benzaldehyde and any other reagents needed to complete the synthesis. show arrows (everything)
20. (8 pts) Provide a synthesis of the following molecule starting from cyclohexene and any other reagent necessary complete the synthesis. Any other necessary reagent + -OCH2C3 20. (8 pts)...
20. (8 pts) Provide a synthesis of the following molecule starting from cyclohexene and any other reagent necessary complete the synthesis. Any other necessary reagent + -OCH2C3
20. (8 pts) Provide a synthesis of the following molecule starting from cyclohexene and any other reagent necessary complete the synthesis. Any other necessary reagent + -OCH2C3
7. Circle the compounds that could be successfully react with a Grignard reagent as substrates in...
7. Circle the compounds that could be successfully react with a Grignard reagent as substrates in a Grignard synthesis. (5 points) 에 HC) O CH₂ H₃CC-CH3 8. Give the Grignard reagent and carbonyl compound need to make each of the following alcohols. (6 points, 2 each) 9. Circle the compound that would be most acidic (have the lowest pKa, highest Ka) (5 points)
Provide a reasonable synthesis Question (2)- Propose a reasonable synthesis of 9 starting from 7 and...
Provide a reasonable synthesis
Question (2)- Propose a reasonable synthesis of 9 starting from 7 and 8 using any other reagents you might require. (15 pts) OH 7 он
3. t Suggest a synthesis for the following alcohols starting from an aldchyde or a etone...
3. t Suggest a synthesis for the following alcohols starting from an aldchyde or a etone and an appropriate Grignand reagent. Below each taget molecule is the mumber of combinations of Grignard reagent and aldehyde or ketoe that might be used oH on DH 1c) 4. Show bow to bring about the following conversions using a Wittig reaction CH OCH, ocd,
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
6. (8 pts) On each reaction arrow. write the reagents) needed to complete each synthesis Br...
6. (8 pts) On each reaction arrow. write the reagents) needed to complete each synthesis Br - Que — Lol 7. (8 pts) Draw the structures of the carboxylic acid and alcohol needed to form the following ester. cat isopropyl 2-methylbenzoate 8. (6 pts) A triglyceride from rendered beef fat (tallow) is drawn below. Draw the products of saponification of tallow using NaOH. You may use R, R', and R" as a short hand for the long hydrocarbon chains. excess...
a synthesis of each of the following target molecules from the starting reagent synt (8) 4....
a synthesis of each of the following target molecules from the starting reagent synt (8) 4. Sh ow methylenecyclohexane Br CH2 CH3 ?? Br ?? ??
Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting...
Show how you would use Grignard syntheses to prepare the
following alcohols from the indicated starting materials and any
other necessary reagents. Draw the Grignard reagent and any other
organic reagents needed.
11 RUVIUWI Constans i Pendulu Part F Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. ОН -C-CH CH, from C-OCH.CH Draw the molecules on...
6. (18 points total) Synthesis: Devise a synthesis of the following compound from the given starting...
6. (18 points total) Synthesis: Devise a synthesis of the following compound from the given starting materials. You may use any other organic or inorganic reagents you deem necessary but you must use the given starting materials as your only source of carbon in the final compound OH several steps OH MeOH HO
20. (8 pts) Provide a synthesis of the following molecule starting from cyclohexene and any other reagent necessary complete the synthesis. Any other necessary reagent + -OCH2C3
20. (8 pts) Provide a synthesis of the following molecule starting from cyclohexene and any other reagent necessary complete the synthesis. Any other necessary reagent + -OCH2C3
7. Circle the compounds that could be successfully react with a Grignard reagent as substrates in a Grignard synthesis. (5 points) 에 HC) O CH₂ H₃CC-CH3 8. Give the Grignard reagent and carbonyl compound need to make each of the following alcohols. (6 points, 2 each) 9. Circle the compound that would be most acidic (have the lowest pKa, highest Ka) (5 points)
Provide a reasonable synthesis
Question (2)- Propose a reasonable synthesis of 9 starting from 7 and 8 using any other reagents you might require. (15 pts) OH 7 он
3. t Suggest a synthesis for the following alcohols starting from an aldchyde or a etone and an appropriate Grignand reagent. Below each taget molecule is the mumber of combinations of Grignard reagent and aldehyde or ketoe that might be used oH on DH 1c) 4. Show bow to bring about the following conversions using a Wittig reaction CH OCH, ocd,
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
6. (8 pts) On each reaction arrow. write the reagents) needed to complete each synthesis Br - Que — Lol 7. (8 pts) Draw the structures of the carboxylic acid and alcohol needed to form the following ester. cat isopropyl 2-methylbenzoate 8. (6 pts) A triglyceride from rendered beef fat (tallow) is drawn below. Draw the products of saponification of tallow using NaOH. You may use R, R', and R" as a short hand for the long hydrocarbon chains. excess...
a synthesis of each of the following target molecules from the starting reagent synt (8) 4. Sh ow methylenecyclohexane Br CH2 CH3 ?? Br ?? ??
Show how you would use Grignard syntheses to prepare the
following alcohols from the indicated starting materials and any
other necessary reagents. Draw the Grignard reagent and any other
organic reagents needed.
11 RUVIUWI Constans i Pendulu Part F Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. ОН -C-CH CH, from C-OCH.CH Draw the molecules on...
6. (18 points total) Synthesis: Devise a synthesis of the following compound from the given starting materials. You may use any other organic or inorganic reagents you deem necessary but you must use the given starting materials as your only source of carbon in the final compound OH several steps OH MeOH HO
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