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Please show all the steps and
explain
correct answer will be rated
yclohexene reacts with NBS...
please show all steps and most important, please explain what's going on here. I'm most confused...
please show all steps and most important, please explain
what's going on here. I'm most confused about the last step, but my
entire understanding of this problem could use work. thank you in
advance
15) (7 points) Draw the intermediates (A and B) and the product (C) of the cyclopentene using the following reagents (no need to draw the mechanism). For each molecule (A, B and C), draw the stereochemistry of the 2 chiral centers that were formed A C...
Quickly show all steps and answers all parts of the question please thank you 2. Show...
Quickly show all steps and answers all parts of the question
please thank you
2. Show the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CH3 OH conc. HBO CH₂ H₂CX Br CH₂ H3C CHE H₃C CH Swi condition Br L CH3 CH3 H₃C HC X X
Please show all of your steps. Thank you! 5 (20 pts). (a) Propose a reasonable synthesis,...
Please show all of your steps.
Thank you!
5 (20 pts). (a) Propose a reasonable synthesis, using indicated diketone as starting material. ini ² and any C4 or less starting materials (SMS) (any reagents are allowed) Hint: as a C3 SM use Br (b) Propose two syntheses, which will use two distinct methods for construction of the 6-membered ring: (1) Crossed-Claisen condensation and (2) Claisen condensation(s). must use this reagent plus any acyclic Cg or less BONUS (5 pts). In...
please answer all :) 250 Chapter 9 Chapter 9 Practice Test Which of the following reagents...
please answer all :)
250 Chapter 9 Chapter 9 Practice Test Which of the following reagents is the best one to use in order to wing reagents is the best one to use in order to convert methyl alcohol into methy bromide? 2. Br HBr Br NaBr Br* a. what would be the major product obtained from the reaction of the epoxide shown below containing 0.1 M HCI? CH2CH; CH CH3 b. What would be the major product obtained from...
Q: Draw out the mechanism. Please show all steps so I can understand. Thank you! arrow...
Q: Draw out the mechanism. Please show all steps so I can
understand. Thank you!
arrow formalism to describe how the reaction below occurs. Be sure to draw out all reaction intermediates & the movement of all electrons needed to justify the formation of the indicated product. You do not need to add in any reagents that are not shown OR show any other products that could be made but are not shown (focus on showing the mechanism for only...
please Answer in Details showing all the steps. Thank you Look at the following reaction: Toluene...
please Answer in Details showing all the steps.
Thank you
Look at the following reaction: Toluene OH + CH3OH OCH3 + H2O a) What is the effect of each of the given changes (see next page) on the rate of the reaction? The possible answers are: Increases, decreases, remains the same or no more reaction. 1- Decreasing the concentration of CH,OH 2-Using a Dean-Stark apparatus (used to remove water from the reaction mixture) 3- Adding H,SO, to the reaction mixture...
please answer all parts, thanks! 1. More substituted alkenes are more stable than less substituted alkenes....
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
Please neatly show me how to solve these with all the correct steps and explain so...
Please neatly show me how to solve these with all the correct
steps and explain so I can understand the process. Thanks
Part (a) Suppose the force exerted by a spring is F(x) = -kx and
the spring has constant k = 325 N/m. Then suppose a wooden cube
with mass m = 6 kg traveling with an initial velocity on a level
surface with kinetic coefficient of friction 0.250 presses against
the spring and it compresses from x =...
PLEASE SHOW ALL WORK AND PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you! 06 Question (4 points) e See page 574 Comp...
PLEASE SHOW ALL WORK AND
PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you!
06 Question (4 points) e See page 574 Complete the mechanism. All necessary atoms and bonds (that is, those that are involved in the mechanism) are drawn in for you already; do not modify the structures by adding or removing any atoms. 1st attempt See Periodic Table See Hint Add the missing curved arrow notation. e See pa 09 Question (4 points) Predict the organic starting...
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl...
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...
please show all steps and most important, please explain
what's going on here. I'm most confused about the last step, but my
entire understanding of this problem could use work. thank you in
advance
15) (7 points) Draw the intermediates (A and B) and the product (C) of the cyclopentene using the following reagents (no need to draw the mechanism). For each molecule (A, B and C), draw the stereochemistry of the 2 chiral centers that were formed A C...
Quickly show all steps and answers all parts of the question
please thank you
2. Show the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CH3 OH conc. HBO CH₂ H₂CX Br CH₂ H3C CHE H₃C CH Swi condition Br L CH3 CH3 H₃C HC X X
Please show all of your steps.
Thank you!
5 (20 pts). (a) Propose a reasonable synthesis, using indicated diketone as starting material. ini ² and any C4 or less starting materials (SMS) (any reagents are allowed) Hint: as a C3 SM use Br (b) Propose two syntheses, which will use two distinct methods for construction of the 6-membered ring: (1) Crossed-Claisen condensation and (2) Claisen condensation(s). must use this reagent plus any acyclic Cg or less BONUS (5 pts). In...
please answer all :)
250 Chapter 9 Chapter 9 Practice Test Which of the following reagents is the best one to use in order to wing reagents is the best one to use in order to convert methyl alcohol into methy bromide? 2. Br HBr Br NaBr Br* a. what would be the major product obtained from the reaction of the epoxide shown below containing 0.1 M HCI? CH2CH; CH CH3 b. What would be the major product obtained from...
Q: Draw out the mechanism. Please show all steps so I can
understand. Thank you!
arrow formalism to describe how the reaction below occurs. Be sure to draw out all reaction intermediates & the movement of all electrons needed to justify the formation of the indicated product. You do not need to add in any reagents that are not shown OR show any other products that could be made but are not shown (focus on showing the mechanism for only...
please Answer in Details showing all the steps.
Thank you
Look at the following reaction: Toluene OH + CH3OH OCH3 + H2O a) What is the effect of each of the given changes (see next page) on the rate of the reaction? The possible answers are: Increases, decreases, remains the same or no more reaction. 1- Decreasing the concentration of CH,OH 2-Using a Dean-Stark apparatus (used to remove water from the reaction mixture) 3- Adding H,SO, to the reaction mixture...
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
Please neatly show me how to solve these with all the correct
steps and explain so I can understand the process. Thanks
Part (a) Suppose the force exerted by a spring is F(x) = -kx and
the spring has constant k = 325 N/m. Then suppose a wooden cube
with mass m = 6 kg traveling with an initial velocity on a level
surface with kinetic coefficient of friction 0.250 presses against
the spring and it compresses from x =...
PLEASE SHOW ALL WORK AND
PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you!
06 Question (4 points) e See page 574 Complete the mechanism. All necessary atoms and bonds (that is, those that are involved in the mechanism) are drawn in for you already; do not modify the structures by adding or removing any atoms. 1st attempt See Periodic Table See Hint Add the missing curved arrow notation. e See pa 09 Question (4 points) Predict the organic starting...
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...
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