can you give the product for each of these reaction?Homework Answers
alkylhalide reacts with Ken in.presence of DMF it undergoes SN2 reaction
NaH is strong base it removes the proton and forms the nucleophile and it undergoes rearrangement and forms the epoxide
remaining reactions are SN2
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can you give the product for each of these reaction?
CH 3 KCN DMF Cl Br...
the weakest base: CH3 HO HS the fastest in an Syl reaction: (CE)_CACHOSCH (CH3CB (CH.) CHCH(Br)CH, (CH),C(Br)CH (CH...
the weakest base: CH3 HO HS the fastest in an Syl reaction: (CE)_CACHOSCH (CH3CB (CH.) CHCH(Br)CH, (CH),C(Br)CH (CH3)2CHCH Br 2. For each pair of reactions given below indicate which is faster and explain your reasoning. + CHỊ N + C CH3Cl + N CH3 + Ng CH₃N₂ + i CHg. + NaCN CH, CN + Nal DMSO CH3-1 + NaCN C H, CN + Nal Cho (c) CH,0 + CH,CH,Br - HƠ + CHỊCH,Br CH,CH,OCH, + Bril CH,CH,OH + Br...
4) For each of the following reactions, indicate whether the reaction would work well. poorly, or...
4) For each of the following reactions, indicate whether the reaction would work well. poorly, or not at all. In such cases that you predict no production of the indicated product, formulate alternative products. Cl CN HCN H3C-OH NaOH acetone H3CnYCH3 Br OH 40°C CH3 Nal CH3 H3C HaC DMF CH3 CH3
please help! will give rating. thank you! L. 1.CH,Br 2. H,0 M. NaBH CH, OH 0....
please help! will give rating. thank you!
L. 1.CH,Br 2. H,0 M. NaBH CH, OH 0. Brz P. Hz, Pd N. 1. KCN 2. LIAIHA 3. H2O ОН Q. NaOH, Bra B. 1, KCN 2. HCI 3. cat NaOH H2O S. NHA mild H+ I. NH3 NaBH3CN U. 1. CHgMgBr 2. H2O, H Determine the reagents necessary to carry out each of the following transformations. The reagent choices are listed in the text box above this question (reagents L-U). You...
3. Shown below are a series of reactions. Predict the major product for each of them....
3. Shown below are a series of reactions. Predict the major product for each of them. Remember, you will need to first decide whether the reaction occurs by an SN2, SN1, E2, or E1 before you can determine what the product will be. Label each as SN2, SN1, E2, or E1. Hint: First decide whether S2/E2 or S1/E1 is favored, and then decide whether the reaction pathway goes by a substitution or elimination reaction. SN2 / SN1 E2/E1 Na DMSO,rt...
b) CH, CH2 CH CH Br + SH — CHZ CH3 CH, CH, CH, Br + SH" — c) (polar protic solvents) CH, Br + (CH3)3N CH, Br + (CH3)3P...
b) CH, CH2 CH CH Br + SH — CHZ CH3 CH, CH, CH, Br + SH" — c) (polar protic solvents) CH, Br + (CH3)3N CH, Br + (CH3)3P - — d) CH, I + CN- - DMF CHZI + CNC CH3CH20H e) CH I + OH- - CHZI + CH, CO2- (6) 14. Place 1º, 2º, 3º and Methyl carbocations in order from least stable to most stable. What factor(s) account for the stability of the most stable...
Determine the product of the following reaction. 1 L CHOCH "CH Br no reaction H DH...
Determine the product of the following reaction. 1 L CHOCH "CH Br no reaction H DH (D) 8. Which reagent(s) is needed to facilitate the following reaction: (A) H20, (B) 1. Hg(OAc)2 in H2O 2. NaBH4 (C) 1. Hg(OAc), in CH,OH (D) 1.BH; THE 2. NaBH4 2. H2O2, NaOH (E) all of the above would work 9. Which of the following compounds is the final product of the reaction below: CI (A) (B) CHA + 2 mol Cl, in cct...
Draw the major organic product(s) of the following reaction. Br DMF + KCN You do not...
Draw the major organic product(s) of the following reaction. Br DMF + KCN You do not have to consider stereochemistry. . If no reaction occurs, draw the organic starting material. When SN1 & El pathways compete, show both the substitution and the elimination products. - Separate multiple products using the+ sign from the drop-down menu. . Do not include counter-ions, e.g., Na, I, in your answer ору 8ste ChemDoodle
5. Consider the rate equati concentration of KCN were doubled? er the rate equation of the...
5. Consider the rate equati concentration of KCN were doubled? er the rate equation of the following reaction. How would the rate be affected if the CH-CH=CHCl + KCN – CHỊCH-CH-CN + KCl a. The rate would be doubled b. The rate would be halved c. The rate would remain the same d. It depends on the solvent 6. What is the major organic product of the reaction below? НВК HOOH, light 1 Br 2 Br b. 2 a. 1...
1. Determine whether the following reactions go through SN or SNP and write the products, with...
1. Determine whether the following reactions go through SN or SNP and write the products, with stereochemistry as applicable. BrNHz NaOEt Nal OMS KCN CI DMSO Br HO NaSH DMSO Tso CH3 Nal Acetone CH3 2. The following reactions each undergo SNmechanisms. For each explain why you would predict the substitution products to come from an SN2mechanism and fill in the product. If stereochemistry is given in the reactants, give the correct stereochemistry in the products. Cl + Z Na...
9.13 Draw a structural formula for the product of each S 2 reaction. Where configuration of...
9.13 Draw a structural formula for the product of each S 2 reaction. Where configuration of the starting material is given, show the configuration of the product. (a) CH,CH,CH,Cl + CH,CH,O-Nat - (b) (CH3)3N + CHI acetone (c) CHBr + Na*CN- acetone CI + CH2S+Na+ - (d) HC ethanol (e) CHỊCH,CH,Cl + CHỤC=C Li* ( -chĄC + NH; echanol diethyl ether (g) 0 NH + CH3(CHỊ) CHỊC14 (h) CH CH.CH,Br + NaCN to acetone 9.16 Treatment of 1-aminoadamantane, CH, N,...
the weakest base: CH3 HO HS the fastest in an Syl reaction: (CE)_CACHOSCH (CH3CB (CH.) CHCH(Br)CH, (CH),C(Br)CH (CH3)2CHCH Br 2. For each pair of reactions given below indicate which is faster and explain your reasoning. + CHỊ N + C CH3Cl + N CH3 + Ng CH₃N₂ + i CHg. + NaCN CH, CN + Nal DMSO CH3-1 + NaCN C H, CN + Nal Cho (c) CH,0 + CH,CH,Br - HƠ + CHỊCH,Br CH,CH,OCH, + Bril CH,CH,OH + Br...
4) For each of the following reactions, indicate whether the reaction would work well. poorly, or not at all. In such cases that you predict no production of the indicated product, formulate alternative products. Cl CN HCN H3C-OH NaOH acetone H3CnYCH3 Br OH 40°C CH3 Nal CH3 H3C HaC DMF CH3 CH3
please help! will give rating. thank you!
L. 1.CH,Br 2. H,0 M. NaBH CH, OH 0. Brz P. Hz, Pd N. 1. KCN 2. LIAIHA 3. H2O ОН Q. NaOH, Bra B. 1, KCN 2. HCI 3. cat NaOH H2O S. NHA mild H+ I. NH3 NaBH3CN U. 1. CHgMgBr 2. H2O, H Determine the reagents necessary to carry out each of the following transformations. The reagent choices are listed in the text box above this question (reagents L-U). You...
3. Shown below are a series of reactions. Predict the major product for each of them. Remember, you will need to first decide whether the reaction occurs by an SN2, SN1, E2, or E1 before you can determine what the product will be. Label each as SN2, SN1, E2, or E1. Hint: First decide whether S2/E2 or S1/E1 is favored, and then decide whether the reaction pathway goes by a substitution or elimination reaction. SN2 / SN1 E2/E1 Na DMSO,rt...
b) CH, CH2 CH CH Br + SH — CHZ CH3 CH, CH, CH, Br + SH" — c) (polar protic solvents) CH, Br + (CH3)3N CH, Br + (CH3)3P - — d) CH, I + CN- - DMF CHZI + CNC CH3CH20H e) CH I + OH- - CHZI + CH, CO2- (6) 14. Place 1º, 2º, 3º and Methyl carbocations in order from least stable to most stable. What factor(s) account for the stability of the most stable...
Determine the product of the following reaction. 1 L CHOCH "CH Br no reaction H DH (D) 8. Which reagent(s) is needed to facilitate the following reaction: (A) H20, (B) 1. Hg(OAc)2 in H2O 2. NaBH4 (C) 1. Hg(OAc), in CH,OH (D) 1.BH; THE 2. NaBH4 2. H2O2, NaOH (E) all of the above would work 9. Which of the following compounds is the final product of the reaction below: CI (A) (B) CHA + 2 mol Cl, in cct...
Draw the major organic product(s) of the following reaction. Br DMF + KCN You do not have to consider stereochemistry. . If no reaction occurs, draw the organic starting material. When SN1 & El pathways compete, show both the substitution and the elimination products. - Separate multiple products using the+ sign from the drop-down menu. . Do not include counter-ions, e.g., Na, I, in your answer ору 8ste ChemDoodle
5. Consider the rate equati concentration of KCN were doubled? er the rate equation of the following reaction. How would the rate be affected if the CH-CH=CHCl + KCN – CHỊCH-CH-CN + KCl a. The rate would be doubled b. The rate would be halved c. The rate would remain the same d. It depends on the solvent 6. What is the major organic product of the reaction below? НВК HOOH, light 1 Br 2 Br b. 2 a. 1...
1. Determine whether the following reactions go through SN or SNP and write the products, with stereochemistry as applicable. BrNHz NaOEt Nal OMS KCN CI DMSO Br HO NaSH DMSO Tso CH3 Nal Acetone CH3 2. The following reactions each undergo SNmechanisms. For each explain why you would predict the substitution products to come from an SN2mechanism and fill in the product. If stereochemistry is given in the reactants, give the correct stereochemistry in the products. Cl + Z Na...
9.13 Draw a structural formula for the product of each S 2 reaction. Where configuration of the starting material is given, show the configuration of the product. (a) CH,CH,CH,Cl + CH,CH,O-Nat - (b) (CH3)3N + CHI acetone (c) CHBr + Na*CN- acetone CI + CH2S+Na+ - (d) HC ethanol (e) CHỊCH,CH,Cl + CHỤC=C Li* ( -chĄC + NH; echanol diethyl ether (g) 0 NH + CH3(CHỊ) CHỊC14 (h) CH CH.CH,Br + NaCN to acetone 9.16 Treatment of 1-aminoadamantane, CH, N,...
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