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(5 pts) Which of the following reactions is expected to produce 1-propanol (CH3CH2CH2OH) at the faster...
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and...
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
11. For each of the following reactions, predict whether Syl or Sy2 will be the primary...
11. For each of the following reactions, predict whether Syl or Sy2 will be the primary substitution mechanism. (Circle one) Br Nal in H2O - SN or SN2 CH,OH Sn1 or SN2 NaCN in DMSO Sn1 or S2 12. For the second reaction in question 11 (above), which do you think would react faster--the sec- ondary bromide or a secondary chloride (assuming the same reaction conditions)? (Circle one) Bromide Chloride Neither (rates are the same)
For the following substitution reactions, choose whether reaction A or B will proceed more quickly. If...
For the following substitution reactions, choose whether reaction A or B will proceed more quickly. If they will proceed at the same rate, put an equal sign,"=", in the box. Reaction Pair Faster? SN1 or SN2? A: CH3Br + CH30-→ CH3OCH3 + Br- B: CH3Br + CH3OH → CH3OCH3 + Br- + H+ Cl + NH3 NH + Cl + H+ B: Ya + Ho — you +C+++11+ OH + Cl + H+ I + NH3 NH2 +I+H+ SN2 ci...
the second one is incorrect here are the multiple choice options. please provide detailed explantion with...
the second one is incorrect
here are the multiple choice options. please provide detailed
explantion with your answer. thanks
Map Consider the following pair of reactions, Predict the type of substitution mechanism, predict which reaction of the pair will occur at the faster rate, and draw the correct organic product. C: + DMSO SN2/faster W + H2O SN1/slower Incorrect Consider the substitution in the substrate. Can it undergo unimolecular substitution? Consider the following pair of reactions, Predict the type of...
In the substitution reactions below, draw the major product in the box provided and indicate in...
In the substitution reactions below, draw the major product in the box provided and indicate in the small box whether the reaction is SN1, SN2, or neither. Be sure to show all stereochemistry. If more than one enantiomer is produced, write "+Enant" in the box with the product. [10] Product SN1/SN2/Neither NaCN Br DMSO NaOEt EtOH Br NaOMe MeOH NaOH Expensive Acetonitrile CH,Br DMF Nat
Q1) provide the product for the following reactions, identify as Sn1,Sn2, E1 or E2. Also provide...
Q1) provide the product for the following reactions, identify as Sn1,Sn2, E1 or E2. Also provide the mechanism of the reaction H20 Br NaCN DMSO b). Csi Меон сін C)- KOH ci H d)_ this reaction was run at 100°C and 0.1 M KOH concentration 2) Rank the members of the following groups in order of basicity, nucleophilicity, and leaving group ability. Expain your answers a) H20, OH, CH,CO2- b) Br", ".Fr 3) Predict the effect of the changes given...
For each of the following pair of reactions, CIRCLE the reaction that will occur faster (A...
For each of the following pair of reactions, CIRCLE the reaction that will occur faster (A or B) 2. NaOH NaOH 2 CH3CH2ONa EtOH CH3CH2ONa Br NaCN NaCN
answer all 1. In each of the following, indicate which S2 reaction will occur faster. Explain...
answer all
1. In each of the following, indicate which S2 reaction will occur faster. Explain your reasoning. a. 1-bromo-2,2-dimethylpropane or 1-bromo-3-methylbutane with Nal in DMSO. b. 1-iodopentane with NaN, in ethanol or NaSCH, in ethanol, c. Reaction of isobutyl iodide with NaBr in acetone or in ethanol. 2. In each of the following, indicate which S, 1 reaction will occur faster. Explain your reasoning. a. Reaction of I-chloro-1-methylcyclohexane or 1-chloro-2-methylcyclohexane in aqueous ethanol. b. Reaction of 2-chloropentane or 3-bromohexane...
2. For each of the chemical substitution reactions below identify the major products and whether the...
2. For each of the chemical substitution reactions below identify the major products and whether the reaction is likely an SNI or SN2. Br NaCN ethanol-water CH,OH /H,0 Nal (1 equiv) acetone CH,CH,OH 25°C 3. For each of the following compounds provide appropriate reactants and solvent systems to synthesize them by a substitution reaction. Show which type of substitution: Syl or SN2. SH
5. 8 marks) Which reaction, 1, 2, or 3 in each group, will be either faster...
5. 8 marks) Which reaction, 1, 2, or 3 in each group, will be either faster or more likely to succeed in forming significant amounts of desired product. Give a brief, but clear and Y concise explanation for all your choices Reaction 1 Br NACN DMSO NaCN Reaction 2 сн,снон NaCN CH,CH,OH Reaction 3 Fastest or most likely or least likely Why? Reaction 1 CH3COONa* acetone CHO Na acetone Reaction 2 Reaction 3 ~ CH,COONa+ Br acetone Fastest or most...
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
11. For each of the following reactions, predict whether Syl or Sy2 will be the primary substitution mechanism. (Circle one) Br Nal in H2O - SN or SN2 CH,OH Sn1 or SN2 NaCN in DMSO Sn1 or S2 12. For the second reaction in question 11 (above), which do you think would react faster--the sec- ondary bromide or a secondary chloride (assuming the same reaction conditions)? (Circle one) Bromide Chloride Neither (rates are the same)
For the following substitution reactions, choose whether reaction A or B will proceed more quickly. If they will proceed at the same rate, put an equal sign,"=", in the box. Reaction Pair Faster? SN1 or SN2? A: CH3Br + CH30-→ CH3OCH3 + Br- B: CH3Br + CH3OH → CH3OCH3 + Br- + H+ Cl + NH3 NH + Cl + H+ B: Ya + Ho — you +C+++11+ OH + Cl + H+ I + NH3 NH2 +I+H+ SN2 ci...
the second one is incorrect
here are the multiple choice options. please provide detailed
explantion with your answer. thanks
Map Consider the following pair of reactions, Predict the type of substitution mechanism, predict which reaction of the pair will occur at the faster rate, and draw the correct organic product. C: + DMSO SN2/faster W + H2O SN1/slower Incorrect Consider the substitution in the substrate. Can it undergo unimolecular substitution? Consider the following pair of reactions, Predict the type of...
In the substitution reactions below, draw the major product in the box provided and indicate in the small box whether the reaction is SN1, SN2, or neither. Be sure to show all stereochemistry. If more than one enantiomer is produced, write "+Enant" in the box with the product. [10] Product SN1/SN2/Neither NaCN Br DMSO NaOEt EtOH Br NaOMe MeOH NaOH Expensive Acetonitrile CH,Br DMF Nat
Q1) provide the product for the following reactions, identify as Sn1,Sn2, E1 or E2. Also provide the mechanism of the reaction H20 Br NaCN DMSO b). Csi Меон сін C)- KOH ci H d)_ this reaction was run at 100°C and 0.1 M KOH concentration 2) Rank the members of the following groups in order of basicity, nucleophilicity, and leaving group ability. Expain your answers a) H20, OH, CH,CO2- b) Br", ".Fr 3) Predict the effect of the changes given...
For each of the following pair of reactions, CIRCLE the reaction that will occur faster (A or B) 2. NaOH NaOH 2 CH3CH2ONa EtOH CH3CH2ONa Br NaCN NaCN
answer all
1. In each of the following, indicate which S2 reaction will occur faster. Explain your reasoning. a. 1-bromo-2,2-dimethylpropane or 1-bromo-3-methylbutane with Nal in DMSO. b. 1-iodopentane with NaN, in ethanol or NaSCH, in ethanol, c. Reaction of isobutyl iodide with NaBr in acetone or in ethanol. 2. In each of the following, indicate which S, 1 reaction will occur faster. Explain your reasoning. a. Reaction of I-chloro-1-methylcyclohexane or 1-chloro-2-methylcyclohexane in aqueous ethanol. b. Reaction of 2-chloropentane or 3-bromohexane...
2. For each of the chemical substitution reactions below identify the major products and whether the reaction is likely an SNI or SN2. Br NaCN ethanol-water CH,OH /H,0 Nal (1 equiv) acetone CH,CH,OH 25°C 3. For each of the following compounds provide appropriate reactants and solvent systems to synthesize them by a substitution reaction. Show which type of substitution: Syl or SN2. SH
5. 8 marks) Which reaction, 1, 2, or 3 in each group, will be either faster or more likely to succeed in forming significant amounts of desired product. Give a brief, but clear and Y concise explanation for all your choices Reaction 1 Br NACN DMSO NaCN Reaction 2 сн,снон NaCN CH,CH,OH Reaction 3 Fastest or most likely or least likely Why? Reaction 1 CH3COONa* acetone CHO Na acetone Reaction 2 Reaction 3 ~ CH,COONa+ Br acetone Fastest or most...
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