Homework Answers
1) Increase the concentration of Nucleophile.
Because rate of SN2 depends on concentration of Nucleophile but rate of SN1 not depends on it.
2) First reaction. Due to more stability of carbocation through resonance.
3) SN1 . Because Alkyl halide is more substituted.
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Which of the following would increase the proportion of a substitution reaction that proceeds via a...
Which of the following would increase the proportion of a substitution reaction that proceeds via a...
Which of the following would increase the proportion of a substitution reaction that proceeds via a SN2 mechanism, rather than SN1? (choose all correct answers) Group of answer choices Use a less reactive nucleophile. Use a more highly substituted alkyl halide. Increase the concentration of the alkyl halide. Increase the concentration of the nucleophile
Question 21 Which of the following would increase the proportion of a substitution reaction that proceeds...
Question 21 Which of the following would increase the proportion of a substitution reaction that proceeds via a S2 mechanism, rather than Sw1? (choose all correct answers) Use a less reactive nucleophile. Use a more highly substituted alkyl halide. Increase the concentration of the alkyl halide. Increase the concentration of the nucleophile
Question 23 By what mechanism would the following compounds react? Br - ?? Sw1 • 512...
Question 23 By what mechanism would the following compounds react? Br - ?? Sw1 • 512 Question 21 Which of the following would increase the proportion of a substitution reaction that proceeds via a 5x2 mechanism, rather than Sw1? (choose all correct answers) Use a less reactive nucleophile. Use a more highly substituted alkyl halide. Increase the concentration of the alkyl halide. Increase the concentration of the nucleophile
By which mechanism would the following reaction proceed? please explain answer of why each is wrong or right. Thank you....
By
which mechanism would the following reaction proceed? please
explain answer of why each is wrong or right. Thank you.
acetone . + L + BUONa Buona acetone Br OSNI OSN2 Ο Ε1 O E2 OSN1 and E1
consider the Sn1 reaction shown below and answer the following questions. Br Br + CH3OH CH3...
consider the Sn1 reaction shown below and answer the following questions. Br Br + CH3OH CH3 + HBO A. Write the rate law for the reaction. B. Identify the nucleophile, the electrophile, and the reaction solvent. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of the alkyl halide. b. Increasing the concentration of CH3OH. c. Replacing HOCH3 with NaOCH3. d. Changing the alkyl halide from a bromide to an...
2. Consider the Sn1 reaction shown below and answer the following questions. Br K . CHOH...
2. Consider the Sn1 reaction shown below and answer the following questions. Br K . CHOH + CH3OH — Kºchs + HBr CH3 + HBr Ph Ph A. Write the rate law for the reaction. B. Identify the nucleophile, the electrophile, and the reaction solvent. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of the alkyl halide. b. Increasing the concentration of CH3OH. c. Replacing HOCH3 with NaOCH3. d....
Really not sure if the second option should be included or not. Would it actually go...
Really not sure if the second option should be included or not.
Would it actually go by an SN1 mechanism since OH- is considered a
strong nucleophile?
Question 25 4 pts Which of the following reactions would most likely proceed via a SN1 mechanism? (choose all correct answers) CI CH3OH + HBr
Consider the SN2 reaction shown below and answer the following questions. Consider the SN1 reaction shown...
Consider the SN2 reaction shown below and answer the
following questions.
Consider the SN1 reaction shown below and answer the following
questions.
1. Consider the SN2 reaction shown below and answer the following questions. acetone Br NaSCH3 SCH3 NaBr + A. Write the rate law for the reaction B. Identify the nucleophile and the electrophile in the reaction C. State how each of the following factors would affect the rate of the reaction a. Increasing the concentration of 1-bromopropane. b....
2. Consider the Sn1 reaction shown below and answer the following questions. + CH3OH "CH₃ +...
2. Consider the Sn1 reaction shown below and answer the following questions. + CH3OH "CH₃ + HBr A. Write the rate law for the reaction. B. Identify the nucleophile, the electrophile, and the reaction solventi Panther ID...... C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of the alkyl halide. b. Increasing the concentration of CH3OH. c. Replacing HOCH3 with NaOCH3. d. Changing the alkyl halide from a bromide to...
Select which compound is the most reactive in an SN1 reaction Br Select one: O III...
Select which compound is the most reactive in an SN1 reaction Br Select one: O III Assuming no other changes, what is the effect of doubling both the alkyl halide and the nucleophile concentrations in the reaction below? for OH 79 + HB Select one: O a quadruples the rate b. triples the rate c. doubles the rate O d. no change e. rate is halved B. Select which compound is the most reactive in an SN 1 reaction Sel...
Question 21 Which of the following would increase the proportion of a substitution reaction that proceeds via a S2 mechanism, rather than Sw1? (choose all correct answers) Use a less reactive nucleophile. Use a more highly substituted alkyl halide. Increase the concentration of the alkyl halide. Increase the concentration of the nucleophile
Question 23 By what mechanism would the following compounds react? Br - ?? Sw1 • 512 Question 21 Which of the following would increase the proportion of a substitution reaction that proceeds via a 5x2 mechanism, rather than Sw1? (choose all correct answers) Use a less reactive nucleophile. Use a more highly substituted alkyl halide. Increase the concentration of the alkyl halide. Increase the concentration of the nucleophile
By
which mechanism would the following reaction proceed? please
explain answer of why each is wrong or right. Thank you.
acetone . + L + BUONa Buona acetone Br OSNI OSN2 Ο Ε1 O E2 OSN1 and E1
consider the Sn1 reaction shown below and answer the following questions. Br Br + CH3OH CH3 + HBO A. Write the rate law for the reaction. B. Identify the nucleophile, the electrophile, and the reaction solvent. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of the alkyl halide. b. Increasing the concentration of CH3OH. c. Replacing HOCH3 with NaOCH3. d. Changing the alkyl halide from a bromide to an...
2. Consider the Sn1 reaction shown below and answer the following questions. Br K . CHOH + CH3OH — Kºchs + HBr CH3 + HBr Ph Ph A. Write the rate law for the reaction. B. Identify the nucleophile, the electrophile, and the reaction solvent. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of the alkyl halide. b. Increasing the concentration of CH3OH. c. Replacing HOCH3 with NaOCH3. d....
Really not sure if the second option should be included or not.
Would it actually go by an SN1 mechanism since OH- is considered a
strong nucleophile?
Question 25 4 pts Which of the following reactions would most likely proceed via a SN1 mechanism? (choose all correct answers) CI CH3OH + HBr
Consider the SN2 reaction shown below and answer the
following questions.
Consider the SN1 reaction shown below and answer the following
questions.
1. Consider the SN2 reaction shown below and answer the following questions. acetone Br NaSCH3 SCH3 NaBr + A. Write the rate law for the reaction B. Identify the nucleophile and the electrophile in the reaction C. State how each of the following factors would affect the rate of the reaction a. Increasing the concentration of 1-bromopropane. b....
2. Consider the Sn1 reaction shown below and answer the following questions. + CH3OH "CH₃ + HBr A. Write the rate law for the reaction. B. Identify the nucleophile, the electrophile, and the reaction solventi Panther ID...... C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of the alkyl halide. b. Increasing the concentration of CH3OH. c. Replacing HOCH3 with NaOCH3. d. Changing the alkyl halide from a bromide to...
Select which compound is the most reactive in an SN1 reaction Br Select one: O III Assuming no other changes, what is the effect of doubling both the alkyl halide and the nucleophile concentrations in the reaction below? for OH 79 + HB Select one: O a quadruples the rate b. triples the rate c. doubles the rate O d. no change e. rate is halved B. Select which compound is the most reactive in an SN 1 reaction Sel...
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