12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Br2 and draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the X axis. (4 points)
Homework Answers
In this, the kinetic product will be 1,2 substitution and thermodynamic product will be 1,4 substitution as shown below
Thank you
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12. Show the kinetic and thermodynamic product formed in the
reaction of 1,3-dibutene with Br2 and...
with energy* 1 of 1 Show the kinetic and thermodynamic product formed in the reaction of...
with energy*
1 of 1 Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene wit! Br2 and draw an energy diagram for both products. Show both products on the same graph w energy on the Y axis and reaction coordinates on the X axis.' Br2 ether buta-1,3-diene
12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brz and...
12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brz and draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the X axis. (4 points) Br2 ether buta-1,3-diene 11. Show the product and use arrows to show the mechanism for the Nucleophilic Aromatic Substitution Reaction below. Assume benzyne is an intermediate. Just write B: to represent a strong base reacting...
11. Show the product and use arrows to show the mechanism for the Nucleophilic Aromatic Substitution...
11. Show the product and use arrows to show the mechanism for the Nucleophilic Aromatic Substitution Reaction below. Assume benzyne is an intermediate. Just write B: to representa strong base reacting with the aromatic ring. (5 points) strong base NH 12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brzand draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the...
heat two products HBr ether 4- KMnO4 H30 9. Carry out the transformation below. More than...
heat two products HBr ether 4- KMnO4 H30 9. Carry out the transformation below. More than one step will be required. Use any reagents you need. Show all reagents and intermediate structures. (4 points) -OH Br 12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brz and draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the X axis. (4...
a) Fill in the missing diene that would lead to this isomer as the thermodynamic, but...
a) Fill in the missing diene that would lead to this isomer as the thermodynamic, but not the kinetic, product HBr Br .Ph (addition rxn) b) Show the mechanism for the above reaction, including the formation of both kinetic (low temperature) and thermodynamic (higher temperature) products. c) Show the mechanism for the conversion of the kinetic to the thermodynamic product. d) show a reasonable energy curve for this transformation and draw in all structures, including intermediates and transition states
a)...
Draw the kinetic and the thermodynamic addition products formed when one equivalent of HBr reacts with...
Draw the kinetic and the thermodynamic addition products formed
when one equivalent of HBr reacts with the following compound.
(Draw a single product for each. Ignore stereochemical or chiral
isomers.) Note: Is this a symmetric or an asymmetric diene? Will it
matter which end of the diene you protonate first?
Look at this link to see the compound HBr is reacting with:
//img.homeworklib.com/questions/ffc52d80-4303-11ea-bc58-936001b91635.png
**WRITTEN WORK** Label the thermodynamic product and the kinetic product formed in the folle reaction. HB...
**WRITTEN WORK** Label the thermodynamic product and the kinetic product formed in the folle reaction. HB HTML EC
Consider the reaction of 2-methyl-1,3-cyclohexadiene with HCI.
Consider the reaction of 2-methyl-1,3-cyclohexadiene with HCI. Assuming that the reaction takes place at a very low temperature: (a) draw the intermediate and product structures, Including any formal charges. (b) What is the major product of the reaction at very low temperatures? Both products are formed in equal amounts. The 1,2-addition product. The 1,4-addition product. (c) Is the reaction under rate control or equilibrium control under the conditions stated above? The reaction is under rate control (kinetic). The reaction is under equilibrium control (thermodynamic). Unable to determine.
Please show your work The reaction of 1,3-pentadiene with hydrogen chloride (HCI) gives the product shown...
Please show your work
The reaction of 1,3-pentadiene with hydrogen chloride (HCI) gives the product shown below (as a racemate). However, the reaction with deuterium chloride (DCI) produces two products, A and B (also as racemates), and the ratio of these is temperature dependent. Which product, A or B is favored at low temperatures (0°C) and What happens to the ratio at higher temperatures (40°C)? Explain these in terms of kinetic vs thermodynamic control. (20 points d. How might you...
with energy*
1 of 1 Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene wit! Br2 and draw an energy diagram for both products. Show both products on the same graph w energy on the Y axis and reaction coordinates on the X axis.' Br2 ether buta-1,3-diene
12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brz and draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the X axis. (4 points) Br2 ether buta-1,3-diene 11. Show the product and use arrows to show the mechanism for the Nucleophilic Aromatic Substitution Reaction below. Assume benzyne is an intermediate. Just write B: to represent a strong base reacting...
11. Show the product and use arrows to show the mechanism for the Nucleophilic Aromatic Substitution Reaction below. Assume benzyne is an intermediate. Just write B: to representa strong base reacting with the aromatic ring. (5 points) strong base NH 12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brzand draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the...
heat two products HBr ether 4- KMnO4 H30 9. Carry out the transformation below. More than one step will be required. Use any reagents you need. Show all reagents and intermediate structures. (4 points) -OH Br 12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brz and draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the X axis. (4...
a) Fill in the missing diene that would lead to this isomer as the thermodynamic, but not the kinetic, product HBr Br .Ph (addition rxn) b) Show the mechanism for the above reaction, including the formation of both kinetic (low temperature) and thermodynamic (higher temperature) products. c) Show the mechanism for the conversion of the kinetic to the thermodynamic product. d) show a reasonable energy curve for this transformation and draw in all structures, including intermediates and transition states
a)...
Draw the kinetic and the thermodynamic addition products formed
when one equivalent of HBr reacts with the following compound.
(Draw a single product for each. Ignore stereochemical or chiral
isomers.) Note: Is this a symmetric or an asymmetric diene? Will it
matter which end of the diene you protonate first?
Look at this link to see the compound HBr is reacting with:
//img.homeworklib.com/questions/ffc52d80-4303-11ea-bc58-936001b91635.png
**WRITTEN WORK** Label the thermodynamic product and the kinetic product formed in the folle reaction. HB HTML EC
Please show your work
The reaction of 1,3-pentadiene with hydrogen chloride (HCI) gives the product shown below (as a racemate). However, the reaction with deuterium chloride (DCI) produces two products, A and B (also as racemates), and the ratio of these is temperature dependent. Which product, A or B is favored at low temperatures (0°C) and What happens to the ratio at higher temperatures (40°C)? Explain these in terms of kinetic vs thermodynamic control. (20 points d. How might you...
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