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QUESTION 16 What would be the monochlorinated product(s) of this reaction? light ? light A. >95%...
Draw all possible monochlorinated products you'd expect upon treating 2-methylbutane with Cl2 and irradiated with UV...
Draw all possible monochlorinated products you'd expect upon treating 2-methylbutane with Cl2 and irradiated with UV light. Draw all possible monochlorinated products you'd expect upon treating cyclohexane with Cl2 and irradiated with UV light. Predict the product(s) you'd expect when the following molecule is treated with NBS and irradiated with UV light? Draw the allylic radical intermediates you would expect to form as intermediates in the following reaction Br NBS + hv Br Provide the product you'd expect from the...
Provide the product you'd expect from the following reaction? OH SOCIL pyridine Draw the allylic radical...
Provide the product you'd expect from the following reaction? OH SOCIL pyridine Draw the allylic radical intermediates you would expect to form as intermediates in the following reaction NBS "Вг + hv "Вr Predict the product(s) you'd expect when the following molecule is treated with NBS and irradiated with UV light? Draw all possible monochlorinated products you'd expect upon treating cyclohexane with Cl2 and irradiated with UV light. Draw all possible monochlorinated products you'd expect upon treating 2-methylbutane with Cl2...
29. What would be the product of the following reaction? 2-Hexyne + 1 equivalent of HCI->...
29. What would be the product of the following reaction? 2-Hexyne + 1 equivalent of HCI-> b) Chloroalkene Chloroalkyne Chloroalkane Alcohol
what is the major product of this reaction? 1 equivalent HCL/ -80 degree C -> Moving...
what is the major product of this reaction? 1 equivalent HCL/
-80 degree C
-> Moving to another question will save this response. Question 16 What is the major product of this reaction seque 1 equiv HCI -80°C B. MacBook Pr 000 What is the product of this reaction? 1) LiAlH(O'Bu) 2) H₂O OH A. OH OM OH MacBook Pro OF?
Predict the substitution product(s) for each of the following reactions and mechanisms by which they are...
Predict the substitution product(s) for each of the following reactions and mechanisms by which they are formed. If no reaction is expected, write no (a) (R)-2-bromobutane with sodium iodide in acetone (b) (R)-3-bromo-3-methylhexane with H20 (c) trans-1-bromo-2-ethylcyclopentane with potassium ethoxide in ethanol (d) trans-1-bromo-3-methylcyclopentane with Nal in acetone 5. For the following set of compounds, predict the order of reactivity with sodium iodide in acetone solution (list them in increasing order of reactivity). C. D. 2-bromobutane 1-chlorobutane 2-chloro-3-methylbutane 2-bromo-2-methylpropane 1-bromobutane...
3. for each of the following, choose the reaction that would proceed more rapidly and give...
3. for each of the following, choose the reaction that would proceed more rapidly and give an explanation for your choice: (a) iodomethane or bromomethane with aqueous KOH (b) iodomethane or iodoethane with aqueous KOH (c) methanol or bromomethane with Nal dissolved in acetone (d) 2-bromopropane or 1-bromopropane with Nal dissolved in acetone (e) 2-bromo-2-methylbutane or 2-bromo-3-methylbutane with ethanol (f) aqueous KBr or aqueous HBr with butanol (g) 2-chloro-3,3-dimethylbutane or 2-chloro-3-methylbutane with potassium tert- butoxide (h) 1:1 or 1:4 by...
Arrange the following chloroalkanes in order of increasing reactivity towards a S_N1 reaction: 1-chloro-2-methylbutane, 1-chloro-3-methylbutane, 2-chloro-2-methylbutane,...
Arrange the following chloroalkanes in order of increasing reactivity towards a S_N1 reaction: 1-chloro-2-methylbutane, 1-chloro-3-methylbutane, 2-chloro-2-methylbutane, 1-chloropentane (A complete answer will provide a bond line drawing of each of the compounds listed) For the same compounds found in question 1, list them in order of increasing reactivity towards an S_N2 reaction (list them as structures as well) Provide a bond line drawing of the product for the following reactions: (answer on back) a. (2S)-2-bromobutane + NaCN in acetone b. (3R)-3-iodo-1...
If you did an SN2 reaction with R-2-bromobutane what would the stereochemistry of the product be?...
If you did an SN2 reaction with R-2-bromobutane what would the stereochemistry of the product be? a) R b) S c) achiral d) racemic mixture e) NA If you did an SN1 reaction with S-3-bromohexane what would the stereochemistry of the product be a) R b) S c) achiral d) racemic mixture e) NA
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....
1.88 pts Question 2 u The structure of the anthelmintic (worm medicine) C-santonin is shown below....
1.88 pts Question 2 u The structure of the anthelmintic (worm medicine) C-santonin is shown below. What is the unsaturation number of a-santonin? CH PICH b) 5 c) 6 d) 7 o b) ) d) o e) Question 6 1.88 pts Alkenes a) have lower boiling points than alcohols of similar molar mass. b) are more dense than alcohols of similar molar mass. c) react via the sigma bond of the carbon-carbon double bond. d) both (a) and (b) e)...
Draw all possible monochlorinated products you'd expect upon treating 2-methylbutane with Cl2 and irradiated with UV light. Draw all possible monochlorinated products you'd expect upon treating cyclohexane with Cl2 and irradiated with UV light. Predict the product(s) you'd expect when the following molecule is treated with NBS and irradiated with UV light? Draw the allylic radical intermediates you would expect to form as intermediates in the following reaction Br NBS + hv Br Provide the product you'd expect from the...
Provide the product you'd expect from the following reaction? OH SOCIL pyridine Draw the allylic radical intermediates you would expect to form as intermediates in the following reaction NBS "Вг + hv "Вr Predict the product(s) you'd expect when the following molecule is treated with NBS and irradiated with UV light? Draw all possible monochlorinated products you'd expect upon treating cyclohexane with Cl2 and irradiated with UV light. Draw all possible monochlorinated products you'd expect upon treating 2-methylbutane with Cl2...
29. What would be the product of the following reaction? 2-Hexyne + 1 equivalent of HCI-> b) Chloroalkene Chloroalkyne Chloroalkane Alcohol
what is the major product of this reaction? 1 equivalent HCL/
-80 degree C
-> Moving to another question will save this response. Question 16 What is the major product of this reaction seque 1 equiv HCI -80°C B. MacBook Pr 000 What is the product of this reaction? 1) LiAlH(O'Bu) 2) H₂O OH A. OH OM OH MacBook Pro OF?
Predict the substitution product(s) for each of the following reactions and mechanisms by which they are formed. If no reaction is expected, write no (a) (R)-2-bromobutane with sodium iodide in acetone (b) (R)-3-bromo-3-methylhexane with H20 (c) trans-1-bromo-2-ethylcyclopentane with potassium ethoxide in ethanol (d) trans-1-bromo-3-methylcyclopentane with Nal in acetone 5. For the following set of compounds, predict the order of reactivity with sodium iodide in acetone solution (list them in increasing order of reactivity). C. D. 2-bromobutane 1-chlorobutane 2-chloro-3-methylbutane 2-bromo-2-methylpropane 1-bromobutane...
3. for each of the following, choose the reaction that would proceed more rapidly and give an explanation for your choice: (a) iodomethane or bromomethane with aqueous KOH (b) iodomethane or iodoethane with aqueous KOH (c) methanol or bromomethane with Nal dissolved in acetone (d) 2-bromopropane or 1-bromopropane with Nal dissolved in acetone (e) 2-bromo-2-methylbutane or 2-bromo-3-methylbutane with ethanol (f) aqueous KBr or aqueous HBr with butanol (g) 2-chloro-3,3-dimethylbutane or 2-chloro-3-methylbutane with potassium tert- butoxide (h) 1:1 or 1:4 by...
Arrange the following chloroalkanes in order of increasing reactivity towards a S_N1 reaction: 1-chloro-2-methylbutane, 1-chloro-3-methylbutane, 2-chloro-2-methylbutane, 1-chloropentane (A complete answer will provide a bond line drawing of each of the compounds listed) For the same compounds found in question 1, list them in order of increasing reactivity towards an S_N2 reaction (list them as structures as well) Provide a bond line drawing of the product for the following reactions: (answer on back) a. (2S)-2-bromobutane + NaCN in acetone b. (3R)-3-iodo-1...
If you did an SN2 reaction with R-2-bromobutane what would the stereochemistry of the product be? a) R b) S c) achiral d) racemic mixture e) NA If you did an SN1 reaction with S-3-bromohexane what would the stereochemistry of the product be a) R b) S c) achiral d) racemic mixture e) NA
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....
1.88 pts Question 2 u The structure of the anthelmintic (worm medicine) C-santonin is shown below. What is the unsaturation number of a-santonin? CH PICH b) 5 c) 6 d) 7 o b) ) d) o e) Question 6 1.88 pts Alkenes a) have lower boiling points than alcohols of similar molar mass. b) are more dense than alcohols of similar molar mass. c) react via the sigma bond of the carbon-carbon double bond. d) both (a) and (b) e)...
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