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1. Provide the reagent needed to convert 2-pentanol to...
Provide the reagent needed to convert 2-pentanol to 2-bromopentane (3 points) 1. Provide the reagent needed...
Provide the reagent needed to convert 2-pentanol to 2-bromopentane (3 points) 1. Provide the reagent needed to complete the reaction below (1 point) 2. CI
Provide the reagent needed to convert 2-pentanol to 2-bromopentane - Provide the reagent needed to complete...
Provide the reagent needed to convert 2-pentanol to 2-bromopentane - Provide the reagent needed to complete the reaction below (1 point)
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyri...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
Provide the missing reagent or major organic product from the following reaction sequence. Take note of...
Provide the missing reagent or major organic product from the following reaction sequence. Take note of the direction of the arrows. Write only the corresponding letters or numbers in the space provided. If the reagent or product is not available then write NONE. Assume aqueous workup is applied at the end of the reaction except for deprotonation reactions. Br 2 PhMgBr х Dess Martin (CH3)2Culi Y REAGENT BANK A. PBrz, Br2 D. NaOEt, EtOH G. CH3OH B. HBr, Br2 E....
1. Consider the reaction of 3-ethyl-2-methyl-3-pentanol with concentrated H SO HCHCH, conc. HSO4 HC-CO-CH.CH heat CH,...
1. Consider the reaction of 3-ethyl-2-methyl-3-pentanol with concentrated H SO HCHCH, conc. HSO4 HC-CO-CH.CH heat CH, OH Show the mechanism and give the product of the reaction.
Please answer ALL parts in simplest form, NO explanation needed, THANK YOU! Part A 1. Which...
Please answer ALL parts in simplest form, NO explanation needed,
THANK YOU!
Part A 1. Which is the strongest acid? a) CH3CH2CH2CH2CH2OH b) CH,CH2CH2CH2COOH C) CH2FCH2CH2CH2COOH d) CH3FCH2CH2CH2CH2OH 2. What is the name of the following alkane? CH3 H₃ C° CH H₂C a) 5,5-dimethylheptane b) 4,4-dimethylheptane c) 2,2-dimethylheptane 1) 3,3-dimethylheptane 3. The name of this alkane is: нс HC ) 3-ethyl-2-methyl-5-propyloctane 6-ethyl-2-methyl-4-propyloctane 3,3-di-methyl-5-ethylactan
QUESTIONS 1. Select a reagent that will distinguish between each pair of compound Write equations for any reaction...
QUESTIONS 1. Select a reagent that will distinguish between each pair of compound Write equations for any reactions that occur. The reagent should react ONLY with one compound of the pair under reaction conditions. Reagent (1) l-propanol zincill 2-propanol OH Equation(s) (2) 2-butanol 2-roethyl-2-propanol (3) 1-propanol 1-chloropropane Popu (4) 1-propanol propene - (5) 2-pentanol 3-pentanol 2. Number the alcohols below according to increasing boiling points. Recall that addition of -CH - usually increases the boiling point by anout thirty degrees...
1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw...
1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw the structure from the provided name: 5-chloro-2,2-dimethylcyclohexane-1,3-dione. 3. (6 points) The following reaction produces five different substitution and elimination products, (a) Draw these products and (b) rank the stability of the elimination products by using the labels (E1-E3) according to the products as you have entered them. substitution product S1 substitution product S2 HzC04 CF, H-OH elimination product E1 elimination product E2 elimination product...
PLEASE answer ALL parts! NO explanations needed! THANK YOU :) Part IV. (a) Please give the...
PLEASE answer ALL parts! NO explanations needed! THANK YOU :)
Part IV. (a) Please give the principle organic product(s) of each reaction, please specify stereochemistry if it applies (18 points) H2SO4 HO Heat 1). BH3. THE 2). H2O2, NaOH HBr Peroxide Brz/H20 CH2Cl2 ? t Brz/hv Bigova NaOCH2CH3 CH3CH2OH, 50 °C HBr Heat OH
HELP PLEASE ANSWER ALL III. Predict the major product(s) or fill in the reagent(s) for the...
HELP PLEASE ANSWER ALL
III. Predict the major product(s) or fill in the reagent(s) for the following reactices. If there is to reaction write NR. (6 points each, 16 points total) Show the correct stresshemistry when needed!! 16 H.CO (excess) CHO HO 17 10 (equiv.) 2) Mes (2 equis.) 18 OH o" 19 1) mCPBA 2) EXON, EICH 20 1) LIAIR (excess) io 2) H 0,1,0 21 1) SNI, 2) CH, Br 3) HBr (2 equiv.) 22.Draw DETAILED arrow.pushing mechanisms...
Provide the reagent needed to convert 2-pentanol to 2-bromopentane (3 points) 1. Provide the reagent needed to complete the reaction below (1 point) 2. CI
Provide the reagent needed to convert 2-pentanol to 2-bromopentane - Provide the reagent needed to complete the reaction below (1 point)
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
Provide the missing reagent or major organic product from the following reaction sequence. Take note of the direction of the arrows. Write only the corresponding letters or numbers in the space provided. If the reagent or product is not available then write NONE. Assume aqueous workup is applied at the end of the reaction except for deprotonation reactions. Br 2 PhMgBr х Dess Martin (CH3)2Culi Y REAGENT BANK A. PBrz, Br2 D. NaOEt, EtOH G. CH3OH B. HBr, Br2 E....
1. Consider the reaction of 3-ethyl-2-methyl-3-pentanol with concentrated H SO HCHCH, conc. HSO4 HC-CO-CH.CH heat CH, OH Show the mechanism and give the product of the reaction.
Please answer ALL parts in simplest form, NO explanation needed,
THANK YOU!
Part A 1. Which is the strongest acid? a) CH3CH2CH2CH2CH2OH b) CH,CH2CH2CH2COOH C) CH2FCH2CH2CH2COOH d) CH3FCH2CH2CH2CH2OH 2. What is the name of the following alkane? CH3 H₃ C° CH H₂C a) 5,5-dimethylheptane b) 4,4-dimethylheptane c) 2,2-dimethylheptane 1) 3,3-dimethylheptane 3. The name of this alkane is: нс HC ) 3-ethyl-2-methyl-5-propyloctane 6-ethyl-2-methyl-4-propyloctane 3,3-di-methyl-5-ethylactan
QUESTIONS 1. Select a reagent that will distinguish between each pair of compound Write equations for any reactions that occur. The reagent should react ONLY with one compound of the pair under reaction conditions. Reagent (1) l-propanol zincill 2-propanol OH Equation(s) (2) 2-butanol 2-roethyl-2-propanol (3) 1-propanol 1-chloropropane Popu (4) 1-propanol propene - (5) 2-pentanol 3-pentanol 2. Number the alcohols below according to increasing boiling points. Recall that addition of -CH - usually increases the boiling point by anout thirty degrees...
1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw the structure from the provided name: 5-chloro-2,2-dimethylcyclohexane-1,3-dione. 3. (6 points) The following reaction produces five different substitution and elimination products, (a) Draw these products and (b) rank the stability of the elimination products by using the labels (E1-E3) according to the products as you have entered them. substitution product S1 substitution product S2 HzC04 CF, H-OH elimination product E1 elimination product E2 elimination product...
PLEASE answer ALL parts! NO explanations needed! THANK YOU :)
Part IV. (a) Please give the principle organic product(s) of each reaction, please specify stereochemistry if it applies (18 points) H2SO4 HO Heat 1). BH3. THE 2). H2O2, NaOH HBr Peroxide Brz/H20 CH2Cl2 ? t Brz/hv Bigova NaOCH2CH3 CH3CH2OH, 50 °C HBr Heat OH
HELP PLEASE ANSWER ALL
III. Predict the major product(s) or fill in the reagent(s) for the following reactices. If there is to reaction write NR. (6 points each, 16 points total) Show the correct stresshemistry when needed!! 16 H.CO (excess) CHO HO 17 10 (equiv.) 2) Mes (2 equis.) 18 OH o" 19 1) mCPBA 2) EXON, EICH 20 1) LIAIR (excess) io 2) H 0,1,0 21 1) SNI, 2) CH, Br 3) HBr (2 equiv.) 22.Draw DETAILED arrow.pushing mechanisms...
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