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what mechanism would this rxn proceed? please explain why each
answer is right or wrong...
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
With explanation please -- thanks! 9. (30 pts) Predict whether the following conditions would mainly proceed...
With explanation please --
thanks!
9. (30 pts) Predict whether the following conditions would mainly proceed via an SN2, SN1, E2, or E1 mechanism (write your answer into box on left). Draw the major product (including enatiomer wher appropriate) in each reaction and show stereochemistry (where appropriate). SN2, SN1 E1, or E2 conc.H2SO4 heat SN2, S1 E1, or E2 H2O SN2, SN1 E1, or E2 NaOEt EtOH, heat SN2, SN1 E1, or E2 v O-CF3 H. KOtBu D. H tBuOH...
explain whether the reaction would more likely proceed via Sn1 or Sn2 mechanism (consider both) H2SO4...
explain whether the reaction would more likely proceed via Sn1
or Sn2 mechanism (consider both)
H2SO4 H2O
please do all and explain sn1 sn2 e1e2 1. Write a full, complete mechanism for each...
please do all and explain sn1 sn2 e1e2
1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: a) ~ Br H2O2 b) 0-5- NaOH NaOCH, 4.5 de the reaction mat occurs more quickly...
FOR EACH QUESTION: 1. Why is the wrong answer wrong? 2. Why is the right answer...
FOR EACH QUESTION:
1. Why is the wrong answer wrong?
2. Why is the right answer right?
3. Which reaction does each problem involve?
#5 What is the correct starting material for the reaction shown? Wrong Answer A CH,COOH #6 Which combination(s) of organic bromide and carbonyl compound can be used to prepare the alcohol in the box by reaction of the Grignard reagent derived from the alkyl bromide with the carbonyl compound? Wrong Answer B a) only 1 b)...
1. indicate whether the following reactions will proceed via an Sni, Sn2, E1 or 2 mechanism....
1. indicate whether the following reactions will proceed via an Sni, Sn2, E1 or 2 mechanism. 2 NISCH reaction type SN NaOCH.CH reaction type 2 2. Briefly explain your answer to question 1b 3. Provide the missing starting material(s), reactant(s) or product(s) as necessary for the following reactions. DBN (a bulky base) Br NaBr B) heat 4. For the following reaction, draw the MAJOR and the MINOR products formed. Label the type of reaction the produced the product below it...
please help me 1. Provide the product/s and mechanism for the following reaction. Explain if the...
please help me
1. Provide the product/s and mechanism for the following reaction. Explain if the reaction condition favors a SN1 or SN2 mechanism. Determine the stereochemistry configuration (S/R) o the product/s. (25 points) NaCN DMSO
My teacher is that A is not the major product. please explain why and what would...
My teacher is that A is not the major product. please explain
why and what would be the major
22) (9 points) For the following reaction: a. (5 points) Draw a complete and detailed mechanism for the process shown below to form compounds A and B. mention whether it is initiation, propagation or termination. b/ (2 points) Explain why this reaction gives a mixture of compounds A and B and does not give compound C c. (2 points) Which product...
Given that the SN2 mechanism requires the nucleophile to force out the leaving group, what would...
Given that the SN2 mechanism requires the nucleophile to force out the leaving group, what would you expect the product ratio of alkyl bromide to alky chloride be when sulfuric acid is the solvent? Also given that the SN1 mechanism requires the nucleophile to react with an empty p orbital of a carbocation involving bond formation, what would you expect the product ratio of alkyl bromide to alky chloride be when sulfuric acid is the solvent? R-Br > R-Cl or...
CAN SOMEONE PLEASE ANSWER THESE FOR ME QUICKLY!!! Name: O Determine wither a reaction proceeds via...
CAN SOMEONE PLEASE ANSWER THESE FOR ME QUICKLY!!!
Name: O Determine wither a reaction proceeds via SN2, SN1, E2, and/or E1/ Predict the productís) of substitution and elimination reactions. Draw the major products), reagent(s), or starting material(s) ¡n order to complete each transformation. Indicate any stereochemistry when appropriate. If there is no reaction, write "NO RXN AND explain why no reaction occurs 1. Br NaCCMe Br b. он NaOE Me DBU d. MeOH e. CI NaSEt Chapter 8-3
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
With explanation please --
thanks!
9. (30 pts) Predict whether the following conditions would mainly proceed via an SN2, SN1, E2, or E1 mechanism (write your answer into box on left). Draw the major product (including enatiomer wher appropriate) in each reaction and show stereochemistry (where appropriate). SN2, SN1 E1, or E2 conc.H2SO4 heat SN2, S1 E1, or E2 H2O SN2, SN1 E1, or E2 NaOEt EtOH, heat SN2, SN1 E1, or E2 v O-CF3 H. KOtBu D. H tBuOH...
explain whether the reaction would more likely proceed via Sn1
or Sn2 mechanism (consider both)
H2SO4 H2O
please do all and explain sn1 sn2 e1e2
1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: a) ~ Br H2O2 b) 0-5- NaOH NaOCH, 4.5 de the reaction mat occurs more quickly...
FOR EACH QUESTION:
1. Why is the wrong answer wrong?
2. Why is the right answer right?
3. Which reaction does each problem involve?
#5 What is the correct starting material for the reaction shown? Wrong Answer A CH,COOH #6 Which combination(s) of organic bromide and carbonyl compound can be used to prepare the alcohol in the box by reaction of the Grignard reagent derived from the alkyl bromide with the carbonyl compound? Wrong Answer B a) only 1 b)...
1. indicate whether the following reactions will proceed via an Sni, Sn2, E1 or 2 mechanism. 2 NISCH reaction type SN NaOCH.CH reaction type 2 2. Briefly explain your answer to question 1b 3. Provide the missing starting material(s), reactant(s) or product(s) as necessary for the following reactions. DBN (a bulky base) Br NaBr B) heat 4. For the following reaction, draw the MAJOR and the MINOR products formed. Label the type of reaction the produced the product below it...
please help me
1. Provide the product/s and mechanism for the following reaction. Explain if the reaction condition favors a SN1 or SN2 mechanism. Determine the stereochemistry configuration (S/R) o the product/s. (25 points) NaCN DMSO
My teacher is that A is not the major product. please explain
why and what would be the major
22) (9 points) For the following reaction: a. (5 points) Draw a complete and detailed mechanism for the process shown below to form compounds A and B. mention whether it is initiation, propagation or termination. b/ (2 points) Explain why this reaction gives a mixture of compounds A and B and does not give compound C c. (2 points) Which product...
CAN SOMEONE PLEASE ANSWER THESE FOR ME QUICKLY!!!
Name: O Determine wither a reaction proceeds via SN2, SN1, E2, and/or E1/ Predict the productís) of substitution and elimination reactions. Draw the major products), reagent(s), or starting material(s) ¡n order to complete each transformation. Indicate any stereochemistry when appropriate. If there is no reaction, write "NO RXN AND explain why no reaction occurs 1. Br NaCCMe Br b. он NaOE Me DBU d. MeOH e. CI NaSEt Chapter 8-3
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