Homework Answers
E2 is the answer...
because weak nucleophiles and Strong base favores E2 reaction ...
Secondary and tertiary halides follow E2 reactions in the presence of base
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QUESTION 16 Consider the reaction shown below to answer questions 16-19. LINR What will be the...
QUESTION 20 Consider the dehydration reaction using the starting material shown below to answer questions 20-23...
QUESTION 20 Consider the dehydration reaction using the starting material shown below to answer questions 20-23 Dehydration Which reagent(s) are required to perform a dehydration reaction? o a. HCI С. NaH o d. H2SO4 e. NaOH f, H2SO4, heat g. NaOH, heat QUESTION 21 Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply iv) a. C. eNone of the above. The reaction goes by an E2 mechanism and no carbocations are formed. QUESTION 22...
Consider the reaction below to answer the following questions. a) Compound B is the S_N2/S_N1/E2/El product...
Consider the reaction below to answer the following questions. a) Compound B is the S_N2/S_N1/E2/El product b) Compound C is the S_N2/S_N1/E2/El product Consider the reaction below to answer the following questions. a) Name the alkyl bromide starting material and classify as either primary, secondary or tertiary. b) Name the product and identify the reaction mechanism as either S_N2/S_N1/E2 El.
What will be the dominant mechanism that occurs in this reaction? CI LiNR2 What will be...
What will be the dominant mechanism that occurs in this
reaction?
CI LiNR2 What will be the dominant mechanism that occurs in this reaction? o a E1 O b. E2
Consider the dehydration reaction using the starting material shown below to answer questions 20-23. НО Dehydration...
Consider the dehydration reaction using the starting material shown below to answer questions 20-23. НО Dehydration Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply. iv) ii) a. i b. d. iv e. None of the above. The reaction goes by an E2 mechanism and no carbocations are formed.
PLEASE ANSWER ALL QUESTIONS Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms....
PLEASE ANSWER ALL QUESTIONS
Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms. The question only requires you to address the E2 reaction only. For the E2 reaction: Use Newman projections to show the relationship between the leaving group and the beta-hydrogen on the carbon labeled with the asterisk ("). 1. If the leaving group and the beta-hydrogen on the carbon labeled with the asterisk (1) are not in the correct orientation, show the result of the...
Please answer all. thanks QUESTION 5 HO Reaction C Reaction D Consider the structural changes that...
Please answer all. thanks
QUESTION 5 HO Reaction C Reaction D Consider the structural changes that take place during Reaction C and Reaction D and the fundamental mechanisms that you identified from the previous question. Fill in the boxes with the missing reagent that is required to complete Reaction C and Reaction D? (Choose only one reagent per reaction.) O Reaction C: HCI Reaction C: Cl2, heat Reaction C: SOCl2 with pyridine Reaction D: KOC(CH3)3 O Reaction D: NaOCH2CH3 Reaction...
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....
Use the reaction below to answer the three questions that follow: SNa DMSO 16. What effect...
Use the reaction below to answer the three questions that follow: SNa DMSO 16. What effect would changing the nucleophile to ethoxide have on the rate of the reaction above? a. The rate would increase. C. The rate would decrease. b. There would be no reaction. d. No effect on rate would be observed. 17. What effect would changing the iodine atom to a chlorine atom have on the rate of the reaction? a. There would be no reaction. c....
please explain why g. Consider the following reaction to answer the questions below. (4pts each) MC...
please explain why
g. Consider the following reaction to answer the questions below. (4pts each) MC CH3OH A) The reaction is likely to proceed via an mechanism. Circle your choice Sw1 S2 E1 E2 B) Would the rate of this reaction increase by switching the nucleophile to CH,O-? YES I NO (Circle one) C) In this reaction, the stereochemistry of the carbon bearing the leaving group would undergo RACEMIZATION / INVERSION / RETENTION of stereochemical configuration (Circle one)
7. Consider the E2 reaction below and answer the following questions. (1) The stereochemistry of carbon 1 is set as...
7. Consider the E2 reaction below and answer the following questions. (1) The stereochemistry of carbon 1 is set as R, but the stereochemistry of carbon 2 is racemic (50% wedge, 50% dash). Predict the two major organic products of the E2 reaction below. Be sure to indicate the stereochemistry of the products. You do not have to draw a mechanism. (6 pts) Base E2 ii) Determine the relationship between the two products above. Circle one. (3 pts). constitutional isomers...
QUESTION 20 Consider the dehydration reaction using the starting material shown below to answer questions 20-23 Dehydration Which reagent(s) are required to perform a dehydration reaction? o a. HCI С. NaH o d. H2SO4 e. NaOH f, H2SO4, heat g. NaOH, heat QUESTION 21 Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply iv) a. C. eNone of the above. The reaction goes by an E2 mechanism and no carbocations are formed. QUESTION 22...
Consider the reaction below to answer the following questions. a) Compound B is the S_N2/S_N1/E2/El product b) Compound C is the S_N2/S_N1/E2/El product Consider the reaction below to answer the following questions. a) Name the alkyl bromide starting material and classify as either primary, secondary or tertiary. b) Name the product and identify the reaction mechanism as either S_N2/S_N1/E2 El.
What will be the dominant mechanism that occurs in this
reaction?
CI LiNR2 What will be the dominant mechanism that occurs in this reaction? o a E1 O b. E2
Consider the dehydration reaction using the starting material shown below to answer questions 20-23. НО Dehydration Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply. iv) ii) a. i b. d. iv e. None of the above. The reaction goes by an E2 mechanism and no carbocations are formed.
PLEASE ANSWER ALL QUESTIONS
Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms. The question only requires you to address the E2 reaction only. For the E2 reaction: Use Newman projections to show the relationship between the leaving group and the beta-hydrogen on the carbon labeled with the asterisk ("). 1. If the leaving group and the beta-hydrogen on the carbon labeled with the asterisk (1) are not in the correct orientation, show the result of the...
Please answer all. thanks
QUESTION 5 HO Reaction C Reaction D Consider the structural changes that take place during Reaction C and Reaction D and the fundamental mechanisms that you identified from the previous question. Fill in the boxes with the missing reagent that is required to complete Reaction C and Reaction D? (Choose only one reagent per reaction.) O Reaction C: HCI Reaction C: Cl2, heat Reaction C: SOCl2 with pyridine Reaction D: KOC(CH3)3 O Reaction D: NaOCH2CH3 Reaction...
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....
Use the reaction below to answer the three questions that follow: SNa DMSO 16. What effect would changing the nucleophile to ethoxide have on the rate of the reaction above? a. The rate would increase. C. The rate would decrease. b. There would be no reaction. d. No effect on rate would be observed. 17. What effect would changing the iodine atom to a chlorine atom have on the rate of the reaction? a. There would be no reaction. c....
please explain why
g. Consider the following reaction to answer the questions below. (4pts each) MC CH3OH A) The reaction is likely to proceed via an mechanism. Circle your choice Sw1 S2 E1 E2 B) Would the rate of this reaction increase by switching the nucleophile to CH,O-? YES I NO (Circle one) C) In this reaction, the stereochemistry of the carbon bearing the leaving group would undergo RACEMIZATION / INVERSION / RETENTION of stereochemical configuration (Circle one)
7. Consider the E2 reaction below and answer the following questions. (1) The stereochemistry of carbon 1 is set as R, but the stereochemistry of carbon 2 is racemic (50% wedge, 50% dash). Predict the two major organic products of the E2 reaction below. Be sure to indicate the stereochemistry of the products. You do not have to draw a mechanism. (6 pts) Base E2 ii) Determine the relationship between the two products above. Circle one. (3 pts). constitutional isomers...
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