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 normalaqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.)Reagents Availablea. benzene/AlCl3 d. H2O, H2SO4g. LiAlH4j. PBг3b. (CH3)2CuLie. H₂, Pd/Ch. NaCNC. CH3NH2f. K* -OC(CH3)3 i. NH3k. Dess-Martin periodinaneI. SOCI₂1-butanolbutanenitrile

To covert butanoic acid to nitrile, we can use reagents g and h. First, we can react butanoic acid…

Answered: ivatives: Nucleophilic Acyl…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter20: Acidity And Pka Of Phenols

Section: Chapter Questions

Problem 11E

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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
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 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
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
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 b. (CH3)2CuLi e. H₂, Pd/C c. CH3NH₂ f. K* -OC(CH3)3 1-bromobutane butanenitrile g. LiAlH4 h. NaCN i. NH3 j. PBr3 k. Dess-Martin periodinane I. SOCI₂
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.
Supply the missing reagent for the following reactions.
CHEMICAL REACTIONS: Illustrate and predict the products of the given chemical reactions below including the correct catalyst for each given reactions Hydration of Propanal.
[Review Topics] [References] 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. H3C CH3 H2O NaOH • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Nat, I', in your answer. • In cases where there is more than one answer, just draw one. C opy aste C. Previous Next Email Instructor Save and Ex Cengage Learning | Cengage Technical Support 5:48 PI 82°F 3/28/20
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. CH3OH H3C CI • • • • 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.

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