Please answer ALL questions and write clearly/neatly with explanations. I will give a positive rating.
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Please answer ALL questions and write clearly/neatly with
explanations. I will give a positive rating.
CEM...
please provide a full explanation on how you got the answers and please answer all of...
please provide a full explanation on how you got the answers and
please answer all of the questions!
1) Name the following compounds: (8 pts) Br 1a) 1b) 2) Draw the major product and write a mechanism for the reaction. (12 pts) Br NaOET EtOH, 60 °C 3) Draw the major product and write a mechanism for the reaction. (10 pts) HBr, 0°C Draw the major product of the reaction shown below. Propose a detailed mechanism for the reaction. HBr...
Please answer all two questions and please explain! I'm completely lost at the moment and I'm...
Please answer all two questions
and please explain! I'm completely lost at the moment and I'm not
sure how to solve it. Please do it step by step if possible.
6. (12 points) Provide products for the reactions shown below. Draw all possible stereoisomers and indicate if the products are achiral, chiral, racemic or meso Br2 Нао Н Br2 CCI 7. (15 points) Predict the major product for the following acid catalyzed hydration reaction, and drawa detailed mechanism using curved...
Could someone please help with these questions. Name: Wittig Post Lab Questions TA Name: Section: 1....
Could someone please help with these questions.
Name: Wittig Post Lab Questions TA Name: Section: 1. Provide the product and/or reagents for the following reactions (3 points, 1 point per question). 1) PPh 2) Butyl Lithium 3) 4-methyl-2-hexanone Br PPha 5. Draw the 'H-NMR for the Wittig product shown below. Label each peak on the NMR to match your product (2 points): D BF А с Е 6 4 3
1. Predict the major product of the reaction. Clearly indicate steroochemistry, if necessary 6 pts) Гомо...
1. Predict the major product of the reaction. Clearly indicate steroochemistry, if necessary 6 pts) Гомо н. Lindlar cat hexanes Me Me 2. Provide reagents to achieve the shown multi-step transformations. (6 pts) ain Name: TA: Section: 3. Draw a detailed arrow.pushing mechanism for the following transformation. (4 pts) HI (excess) нсусн сн.
Please and all two questions and explain how you got to your answer. I'm really lost...
Please and all two questions
and explain how you got to your answer. I'm really lost and I have
an exam in 7 days! A step by step would be appreciated.
6. (10 points) Provide products for the reactions shown below. Draw all possible stereoisomers and indicate if the products are achiral, chiral, racemic or meso. Вrz Hао 1) ВНз-THF 2) H,О, NaOH 7. (10 points) Draw a detailed mechanism using curved arrow notation for the reaction shown below. H2SO4...
major products formed by substitution (Sn1and Sn2) Answer all 4 questions for a total of 100 points. An additional...
major products formed by substitution (Sn1and Sn2)
Answer all 4 questions for a total of 100 points. An additional 8 points is given to the bonus question. 1a) Give the major product formed by the following substitution reactions: (3 points) by Give the major product formed by the following $2 substitution reaction and the mechanism for it formation: (6 points) Н. c) Give the major product formed by the following S1 substitution reactions and the mechanism for its formation: (16...
Organic chemistry mechanisms i need help with systheses questions 6,7,8,9 2-hydroxybenzoic (3 pts) 5. Provide an...
Organic chemistry mechanisms
i need help with systheses questions 6,7,8,9
2-hydroxybenzoic (3 pts) 5. Provide an appropriate structure for: 3,3-dimethylcyclobutanecarbonitrile. (4 pts each, unless otherwise noted, 12 pts total) 6-8. Syntheses: draw / provide the likely organic product(s) generated in each of the reactions (or reaction sequences) below. As appropriate, pay attention to regiospecificity (new bond formation and location in the product formed) and stereochemistry (direction in space of new bond(s) formed). Indicate ALL likely products: where one product does...
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You...
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You do not need to provide any starting material or product, just the reaction conditions (see example below) 1.B Example: Show reagent 'B' followed by aqueous acid: 2. H30 a. Markovnikov addition of H2O to a double bond: b. Anti-Markovnikov addition of H2O to a double bond: c. Markovnikov addition to form an alkyl bromide from an alkene: d. Reaction conditions to change 1,2-dimethylcyclohexene into...
I need the mechanism please. IV. Provide a complete stepwise mechanism for the following reaction sequence,...
I need the mechanism please.
IV. Provide a complete stepwise mechanism for the following reaction sequence, including initiation and termination steps for any radical reactions (i.e. write a continuous reaction mechanism with the product of step 1 being used in step 2.... Draw the product of each step in the indicated boxes. 1) Br2, hv 2) KO Bu/BuOH 3) HBr, ROOR Br step 1 product step 2 product
Please answer all two questions and please explain! I'm completely lost at the moment and I'm...
Please answer all two
questions and please explain! I'm completely lost at the moment and
I'm not sure how to solve it. Please do it step by step if
possible.
10. (10 points) Account for the relative product distribution for the radical bromination reaction shown below. (a) Write the hydrogen abstraction step reaction (radical formation), including the transition state, that leads to each product. (b) Match each reaction to the correct reaction coordinate diagram. Draw the reactants on the energy...
please provide a full explanation on how you got the answers and
please answer all of the questions!
1) Name the following compounds: (8 pts) Br 1a) 1b) 2) Draw the major product and write a mechanism for the reaction. (12 pts) Br NaOET EtOH, 60 °C 3) Draw the major product and write a mechanism for the reaction. (10 pts) HBr, 0°C Draw the major product of the reaction shown below. Propose a detailed mechanism for the reaction. HBr...
Please answer all two questions
and please explain! I'm completely lost at the moment and I'm not
sure how to solve it. Please do it step by step if possible.
6. (12 points) Provide products for the reactions shown below. Draw all possible stereoisomers and indicate if the products are achiral, chiral, racemic or meso Br2 Нао Н Br2 CCI 7. (15 points) Predict the major product for the following acid catalyzed hydration reaction, and drawa detailed mechanism using curved...
Could someone please help with these questions.
Name: Wittig Post Lab Questions TA Name: Section: 1. Provide the product and/or reagents for the following reactions (3 points, 1 point per question). 1) PPh 2) Butyl Lithium 3) 4-methyl-2-hexanone Br PPha 5. Draw the 'H-NMR for the Wittig product shown below. Label each peak on the NMR to match your product (2 points): D BF А с Е 6 4 3
1. Predict the major product of the reaction. Clearly indicate steroochemistry, if necessary 6 pts) Гомо н. Lindlar cat hexanes Me Me 2. Provide reagents to achieve the shown multi-step transformations. (6 pts) ain Name: TA: Section: 3. Draw a detailed arrow.pushing mechanism for the following transformation. (4 pts) HI (excess) нсусн сн.
Please and all two questions
and explain how you got to your answer. I'm really lost and I have
an exam in 7 days! A step by step would be appreciated.
6. (10 points) Provide products for the reactions shown below. Draw all possible stereoisomers and indicate if the products are achiral, chiral, racemic or meso. Вrz Hао 1) ВНз-THF 2) H,О, NaOH 7. (10 points) Draw a detailed mechanism using curved arrow notation for the reaction shown below. H2SO4...
major products formed by substitution (Sn1and Sn2)
Answer all 4 questions for a total of 100 points. An additional 8 points is given to the bonus question. 1a) Give the major product formed by the following substitution reactions: (3 points) by Give the major product formed by the following $2 substitution reaction and the mechanism for it formation: (6 points) Н. c) Give the major product formed by the following S1 substitution reactions and the mechanism for its formation: (16...
Organic chemistry mechanisms
i need help with systheses questions 6,7,8,9
2-hydroxybenzoic (3 pts) 5. Provide an appropriate structure for: 3,3-dimethylcyclobutanecarbonitrile. (4 pts each, unless otherwise noted, 12 pts total) 6-8. Syntheses: draw / provide the likely organic product(s) generated in each of the reactions (or reaction sequences) below. As appropriate, pay attention to regiospecificity (new bond formation and location in the product formed) and stereochemistry (direction in space of new bond(s) formed). Indicate ALL likely products: where one product does...
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You do not need to provide any starting material or product, just the reaction conditions (see example below) 1.B Example: Show reagent 'B' followed by aqueous acid: 2. H30 a. Markovnikov addition of H2O to a double bond: b. Anti-Markovnikov addition of H2O to a double bond: c. Markovnikov addition to form an alkyl bromide from an alkene: d. Reaction conditions to change 1,2-dimethylcyclohexene into...
I need the mechanism please.
IV. Provide a complete stepwise mechanism for the following reaction sequence, including initiation and termination steps for any radical reactions (i.e. write a continuous reaction mechanism with the product of step 1 being used in step 2.... Draw the product of each step in the indicated boxes. 1) Br2, hv 2) KO Bu/BuOH 3) HBr, ROOR Br step 1 product step 2 product
Please answer all two
questions and please explain! I'm completely lost at the moment and
I'm not sure how to solve it. Please do it step by step if
possible.
10. (10 points) Account for the relative product distribution for the radical bromination reaction shown below. (a) Write the hydrogen abstraction step reaction (radical formation), including the transition state, that leads to each product. (b) Match each reaction to the correct reaction coordinate diagram. Draw the reactants on the energy...
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