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Outline the synthesis of the following compounds from the compound given. 4-nitro-2, 6-dibromoanisole from anisole. 4-bromo-2-nitrobenzoic...
Outline all steps in the laboratory synthesis of the following compounds from benzene and/or toluene, using...
Outline all steps in the laboratory synthesis of the following compounds from benzene and/or toluene, using any needed aliphatic or inorganic reagents. Assume the para isomer can be separated from an ortho,para mixture. Do not show mechanisms. p-bromobenzoic acid m-bromobenzoic acid 2-bromo-4-nitrotoluene 2-bromo-4-nitrobenzoic acid 4-bromo-3-nitrobenzoic acid o-iodobenzoic acid
Outline a synthesis of the following compound from the compounds below as the only source of carb...
using basic reactions and
grignard.
Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3
Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3
2. Outline a synthesis starting from the compound compounds. Fill in the missing reagents and compound...
2. Outline a synthesis starting from the compound compounds. Fill in the missing reagents and compound sis starting from the compound hatow and any other organ ther organic/inorganic PBry COOH
3. Write the structure of following organic compounds (15 points) 3-Chloro-5,7-dimethyl-4-cyclopropyl-2-octene 2-amino-3-methyl-2-nitro-butanal 2-Bromo-4-nitro-3-hexanol Aminomethanamide 2-Chloro-3-methyl-1-cyclopentanone 2-bromo-3-methyl-2-pentene...
3. Write the structure of following organic compounds (15 points) 3-Chloro-5,7-dimethyl-4-cyclopropyl-2-octene 2-amino-3-methyl-2-nitro-butanal 2-Bromo-4-nitro-3-hexanol Aminomethanamide 2-Chloro-3-methyl-1-cyclopentanone 2-bromo-3-methyl-2-pentene 1-ethyl-3-methyl-2-propylcyclopentane 2-Keto-1,3-propandioic acid
12. Which compound is the strongest acid? 11. Which compound is the strongest base? (A) benzoic a...
12. Which compound is the strongest acid? 11. Which compound is the strongest base? (A) benzoic acid (B) 4-amino-2-methylbenzoic acid ©p-nitrobenzoic acid (A) m-nitroaniline (B) aniline 4-methylaniline 3-bromo-5-nitroaniline 24-dimethylaniline po 13. Which of the following compounds E)3.S-dinitrobenzoic acid is has the 4.ow many Ha atoms are in the compound: 14 cyclohexane-1,3-dione? (A) 2 (B) 4 (C)5 highest number of alpha hydrogen? (A) 2,4-dimethyl-3-hexanone (B) cyclohexanone C) benzaldehyde D) 2-heptanone (E) propanone IS. Which of the following compounds has the16. Which...
Draw the mechanism and label products and reactants for the synthesis of aniline to 4-Bromo-2-Chloroacetanilide: Aniline...
Draw the mechanism and label products and reactants for the synthesis of aniline to 4-Bromo-2-Chloroacetanilide: Aniline + Acetic Anhydride --> Acetanilide + Acetic Acid Acetanilide + Bromine --> 4-Bromoacetanilide STEP 1: Hydrochloric Acid + Sodium Chlorate --> Chlorine + Water + Sodium Chloride STEP 2: 4-Bromoacetanilide + Chlorine --> 4-Bromo-2-Chloroacetanilide 4-Bromo-2-Chloroacetanilide + Ethanol --> 4-Bromo-2-Chloroaniline + Ethyl Acetate Show all lone pairs or formal charges.
outline labratory syntheses of each of the following compounds starting with benzene and any other reagents...
outline labratory syntheses of each of the following compounds
starting with benzene and any other reagents
Outline laboratory syntheses of each of the following compounds, starting with benzene and any other reagents. (c) CI (a) p-nitrotoluene (b) p-dibromobenzene (c) p-chloroacetophenone (d) m-nitrobenzenesulfonic acid (e) p-chloronitrobenzene (f) 1,3,5-trinitrobenzene (g) 2,6-dibromo-4-nitrotoluene
2. Draw the structures of the following compounds m-nitrobenzoic acid o-bromoaniline Dojannolane The concept of aromaticity...
2. Draw the structures of the following compounds m-nitrobenzoic acid o-bromoaniline Dojannolane The concept of aromaticity (6 points each) No crt withot coreer ptenaion
solve the following Create a mechanism to produce 4-tert-Butylbenzene-1, 2-dicarboxylic acid from o-Xylene possible to get...
solve the following
Create a mechanism to produce 4-tert-Butylbenzene-1, 2-dicarboxylic acid from o-Xylene possible to get multiple products from used mechanisms. Use only the reaction path that yields the final desired product СОН tert Buty benzene 12 licarbon and 6) Chose the starting material from the table and create m-nitroacetophenone. Does it matter which functional group is attached to your starting material first? Give a reason to support your responce 7) Make 3-Bromo-5-nitrobenzoic acid from toluene using reactions from the...
Outline a synthesis of the following compound from the compound below as the only source of carbo...
Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source of carbon
Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source...
using basic reactions and
grignard.
Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3
Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3
2. Outline a synthesis starting from the compound compounds. Fill in the missing reagents and compound sis starting from the compound hatow and any other organ ther organic/inorganic PBry COOH
3. Write the structure of following organic compounds (15 points) 3-Chloro-5,7-dimethyl-4-cyclopropyl-2-octene 2-amino-3-methyl-2-nitro-butanal 2-Bromo-4-nitro-3-hexanol Aminomethanamide 2-Chloro-3-methyl-1-cyclopentanone 2-bromo-3-methyl-2-pentene 1-ethyl-3-methyl-2-propylcyclopentane 2-Keto-1,3-propandioic acid
12. Which compound is the strongest acid? 11. Which compound is the strongest base? (A) benzoic acid (B) 4-amino-2-methylbenzoic acid ©p-nitrobenzoic acid (A) m-nitroaniline (B) aniline 4-methylaniline 3-bromo-5-nitroaniline 24-dimethylaniline po 13. Which of the following compounds E)3.S-dinitrobenzoic acid is has the 4.ow many Ha atoms are in the compound: 14 cyclohexane-1,3-dione? (A) 2 (B) 4 (C)5 highest number of alpha hydrogen? (A) 2,4-dimethyl-3-hexanone (B) cyclohexanone C) benzaldehyde D) 2-heptanone (E) propanone IS. Which of the following compounds has the16. Which...
outline labratory syntheses of each of the following compounds
starting with benzene and any other reagents
Outline laboratory syntheses of each of the following compounds, starting with benzene and any other reagents. (c) CI (a) p-nitrotoluene (b) p-dibromobenzene (c) p-chloroacetophenone (d) m-nitrobenzenesulfonic acid (e) p-chloronitrobenzene (f) 1,3,5-trinitrobenzene (g) 2,6-dibromo-4-nitrotoluene
2. Draw the structures of the following compounds m-nitrobenzoic acid o-bromoaniline Dojannolane The concept of aromaticity (6 points each) No crt withot coreer ptenaion
solve the following
Create a mechanism to produce 4-tert-Butylbenzene-1, 2-dicarboxylic acid from o-Xylene possible to get multiple products from used mechanisms. Use only the reaction path that yields the final desired product СОН tert Buty benzene 12 licarbon and 6) Chose the starting material from the table and create m-nitroacetophenone. Does it matter which functional group is attached to your starting material first? Give a reason to support your responce 7) Make 3-Bromo-5-nitrobenzoic acid from toluene using reactions from the...
Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source of carbon
Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source...
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