[References] From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a r aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) a. benzene/AICI, b. (CH₂)₂Culi C. CHÍNH 1-bromobutane Reagents Available d. H₂O, H₂SO4 e. H₂. Pd/C f. K OC(CH3)3 N-methylpentanamide 9. LIAIH h. NaCN i. NH₂ j. PBrs k. Dess-Martin periodinane I. SOCI₂

[References] From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a r aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) a. benzene/AICI, b. (CH₂)₂Culi C. CHÍNH 1-bromobutane Reagents Available d. H₂O, H₂SO4 e. H₂. Pd/C f. K OC(CH3)3 N-methylpentanamide 9. LIAIH h. NaCN i. NH₂ j. PBrs k. Dess-Martin periodinane I. SOCI₂

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.50P

See similar textbooks

Similar questions

From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.)
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) a. 1-butene b. N-methylpentanamide
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) Reagents Available a. benzene/AlCl³ b. (CH3)2Culi C. CHÍNH, pentanenitrile butanenitrile d. H₂O, H₂SO4 e. H₂, Pd/C f. K* OC(CH3)3 g. LIAIH h. NaCN 1. NH3 j. PBr3 k. Dess-Martin periodinane 1. SOCI₂
ivatives: Nucleophilic Acyl Substitution Reactions - EOC [References] From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) Reagents Available a. benzene/AlCl3 d. H2O, H2SO4 g. LiAlH4 j. PBг3 b. (CH3)2CuLi e. H₂, Pd/C h. NaCN C. CH3NH2 f. K* -OC(CH3)3 i. NH3 k. Dess-Martin periodinane I. SOCI₂ 1-butanol butanenitrile
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) Reagents Available d. H₂O, H₂SO4 e. H₂, Pd/C f. K OC(CH3)3 a. benzene/AICI3 b. (CH3)2CuLi c. CH3NH₂ 1-bromobutane 2-pentanone g. LIAIH4 h. NaCN i. NH3 j. PBr3 k. Dess-Martin periodinane I. SOCI₂ 17
Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. You do not have to consider stereochemistry. Include all valence lone pairs in your answer. Do not include counter-ions, e.g., Na+, I-, in your answer. In cases where there is more than one answer, just draw one.
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) Reagents Available a. benzene/AICI3 d. H20, H2SO4 g. LIAIH4 j. PBr3 b. (CH3)2CuLi е. На, Pd/C h. NaCN k. Dess-Martin periodinane c. CH3NH2 f. K* "OC(CH3)3 i. NH3 I. SOCI, pentanenitrile 2-hexanone
3. Draw the systematic reaction mechanism for between the reaction of isoamyl alcohol and acetic acid. What are the products? What is the functional group of the major product? Does it have a scent? If so, what is the scent smells like?4. Charlie and Daniel wanted to make a drink containing 6.9% ethanol in the laboratory. However, there are three unlabelled reagent bottles that may contain these chemicals: ethanol, cyclohexane, and water. Devise a systematic flow chart to identify the ethanol and water in these three unlabelled reagent bottles.Assuming that the mixture in the reagent bottle containing ethanol are water and ethanol, what is the volume of the ethanol in the 132g of solution?5. Andrea and Yvette are going to cook the most delicious food that ever going to exist for their tired classmates that conducted the experiment in an organic chemistry laboratory. However, the stores are closed and they don’t have a table salt for the seasoning of their special dish so they need to…
Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. CI + H₂N • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. OH • Do not include counter-ions, e.g., Na+, I¯, in your answer. • In cases where there is more than one answer, just draw one.
In the following reaction Series, write down the appropriate reagents that can be used where there are question marks
Complete the following reaction diagram by giving either the reaction conditions or the missing products. The reaction mechanisms are not required.
The following transformation can be accomplished by reactions we have studied in this chapter and Chapter 20. Name the type of reaction used in each step.