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please help with organic chemistry! mechanisms?
5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following...
5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. provide a detailed explanation to...
5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. provide a detailed explanation to the formation of each product. You should use su intermediates in your answer. (8 points). tous seront you. You. .8
help please! for 6 and 7. 6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one...
help please! for 6 and 7.
6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH CH,O to give an elimination product. Provide the structure of this compound and briefly explain why it does not react (5 points). When 4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are formed, with the rearranged product predominating as shown in the diagram that follows. When small amounts of acetate ion are added to the reaction...
4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are urmea, with the rearranged product predominating...
4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are urmea, with the rearranged product predominating as shown in the diagram that follows. When small amounts of acetate ion are added to the reaction mixture, no increase in the rate is observed. Propose a mechanism that accounts for these results. Explain clearly why two products are formed (5 points) Minor Major
5. Explain how the following changes will influence the rate of the reaction of 2-bromo-2- methylbutane...
5. Explain how the following changes will influence the rate of the reaction of 2-bromo-2- methylbutane with methanol: a. The alkyl halide is changed to 2-chloro-2-methylbutane b. The alkyl halide is changed to 2-chloro-3-methylbutane 6. What product(s) do you predict for the following reactions? Be specific with regard to stereochemistry. Also, indicate which stereoisomer will be more predominant. a. R-2-bromopentane + CH30 b. R-3-bromo-3-metylheptane + CH3OH C. 1-bromo-2-butene + CH30 d. 1-bromo-2-butene + CH3OH e. E2 reaction of 2-bromobutane f....
please help me with Organic Chemistry/Alkynes. Thank you! Directions: Place your answers to the following questio...
please help me with Organic Chemistry/Alkynes. Thank you!
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CI CECH A. B sp,sp? sp?sp? sp, sp sp, sp sp, sp E. Ans. - 2. What is the IUPAC name for the molecule shown below? 6b А. B. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne (E)-2-butynyl-2-butene E. Ans. Select the best explanation...
Chemistry Organic Chemistry Problems Elimination Reactions Problem 5: Which of the product in the following reaction...
Chemistry Organic Chemistry Problems Elimination Reactions Problem 5: Which of the product in the following reaction will form and why. Use mechanism and relevant drawings to explain your answer. Br Problem 6: What is the product of the following reaction? sodium methoxide methanol sodium methoxide methanol Organic Chemistry Organic Chemistry Problems Elimination Reactions Problem 10: Use mechanism to explain all of the products for the reaction below. OH H2SO4 heat
pls and ty, (re-upload) alkene reactivity and its effects on stereo Reactivity In this module, we...
pls and ty, (re-upload)
alkene reactivity and its effects on stereo Reactivity In this module, we will look at alkene reactivity reacts with HBr, two products are formed, C and D. stereochemistry. When dode A CHE H-Br OCH, A OCH, Intermediate B OCH OCH C Question 1. (1 point) Draw the arrow pushing mechanism reactants are drawn below - just fill in the arrows. In electrophile (E) leaving group for the synthesis of C. The intermediates and each step. Identity...
please help with these chemistry problems 2. (5 points) Why does this reaction occur via a...
please help with these chemistry problems
2. (5 points) Why does this reaction occur via a Si1 pathway and not via a Si2 pathway? 3. (5 points) In general are SN1 reactions stereospecific? Why or why not? 2 5.(5 points) Why do carbon substituents stabilize a carbocation and destabilize a carbanion? 6. (5 points) The mass spec of your product has a base peak at 77 draw what this fragment looks like. What would explain the peak at 79. (you...
Organic chemistry help! please help 27. (ps) For the following reaction (a) (2pts) Circle the major...
Organic chemistry help! please help
27. (ps) For the following reaction (a) (2pts) Circle the major expected product (b) (5pts) Give the detailed mechanism for the formation of the major product. (Include all steps, intermediates, resonance structures, and electron movement arrows.) (c) pts) Explain important factors related to why one product is fowered -=- Na NHI, 1 +
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...
5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. provide a detailed explanation to the formation of each product. You should use su intermediates in your answer. (8 points). tous seront you. You. .8
help please! for 6 and 7.
6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH CH,O to give an elimination product. Provide the structure of this compound and briefly explain why it does not react (5 points). When 4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are formed, with the rearranged product predominating as shown in the diagram that follows. When small amounts of acetate ion are added to the reaction...
4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are urmea, with the rearranged product predominating as shown in the diagram that follows. When small amounts of acetate ion are added to the reaction mixture, no increase in the rate is observed. Propose a mechanism that accounts for these results. Explain clearly why two products are formed (5 points) Minor Major
5. Explain how the following changes will influence the rate of the reaction of 2-bromo-2- methylbutane with methanol: a. The alkyl halide is changed to 2-chloro-2-methylbutane b. The alkyl halide is changed to 2-chloro-3-methylbutane 6. What product(s) do you predict for the following reactions? Be specific with regard to stereochemistry. Also, indicate which stereoisomer will be more predominant. a. R-2-bromopentane + CH30 b. R-3-bromo-3-metylheptane + CH3OH C. 1-bromo-2-butene + CH30 d. 1-bromo-2-butene + CH3OH e. E2 reaction of 2-bromobutane f....
please help me with Organic Chemistry/Alkynes. Thank you!
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CI CECH A. B sp,sp? sp?sp? sp, sp sp, sp sp, sp E. Ans. - 2. What is the IUPAC name for the molecule shown below? 6b А. B. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne (E)-2-butynyl-2-butene E. Ans. Select the best explanation...
Chemistry Organic Chemistry Problems Elimination Reactions Problem 5: Which of the product in the following reaction will form and why. Use mechanism and relevant drawings to explain your answer. Br Problem 6: What is the product of the following reaction? sodium methoxide methanol sodium methoxide methanol Organic Chemistry Organic Chemistry Problems Elimination Reactions Problem 10: Use mechanism to explain all of the products for the reaction below. OH H2SO4 heat
pls and ty, (re-upload)
alkene reactivity and its effects on stereo Reactivity In this module, we will look at alkene reactivity reacts with HBr, two products are formed, C and D. stereochemistry. When dode A CHE H-Br OCH, A OCH, Intermediate B OCH OCH C Question 1. (1 point) Draw the arrow pushing mechanism reactants are drawn below - just fill in the arrows. In electrophile (E) leaving group for the synthesis of C. The intermediates and each step. Identity...
please help with these chemistry problems
2. (5 points) Why does this reaction occur via a Si1 pathway and not via a Si2 pathway? 3. (5 points) In general are SN1 reactions stereospecific? Why or why not? 2 5.(5 points) Why do carbon substituents stabilize a carbocation and destabilize a carbanion? 6. (5 points) The mass spec of your product has a base peak at 77 draw what this fragment looks like. What would explain the peak at 79. (you...
Organic chemistry help! please help
27. (ps) For the following reaction (a) (2pts) Circle the major expected product (b) (5pts) Give the detailed mechanism for the formation of the major product. (Include all steps, intermediates, resonance structures, and electron movement arrows.) (c) pts) Explain important factors related to why one product is fowered -=- Na NHI, 1 +
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...
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