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heat two products HBr ether 4- KMnO4 H30 9. Carry out the transformation below. More than...
12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Br2 and...
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)
12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Bry and draw an energy diagram for both products. Show both products on the same graph with energy on the Y...
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...
9. Carry out the transformation below. More than one step will be required. Use any reagents...
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)
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
9. Carry out the transformation below. More than one step will be required. Use any reagents...
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 10. 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) BE
10. Carry out the transformation below. More than one step will be required. Use any reagents...
10. 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)
10. 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) Br
13. (12 pts-4 pts each) Show how you could carry out th how you could carry...
13. (12 pts-4 pts each) Show how you could carry out th how you could carry out the following synthesis reactions by placing the letters corresponding to the appropriate reagents above each ar must be in the correct order to receive full credit. priate reagents above each arrow. The reagents A. HBr, ether B. Br2, CH2Cl2 C. Br2, H2O D. 1. Hg(OAC)2, H2O/THF 2. NaBH4 E. 1. BH3, THF 2. H2O2, OH F. H2SO4, H2O/HgSO4 G. NBS, hy H. H/Pd/C...
7-9 please! 4 7. One of the following is much more acidic than the other. Circle...
7-9 please!
4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
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)
12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Bry and draw an energy diagram for both products. Show both products on the same graph with energy on the Y...
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...
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)
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
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 10. 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) BE
10. 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)
10. 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) Br
13. (12 pts-4 pts each) Show how you could carry out th how you could carry out the following synthesis reactions by placing the letters corresponding to the appropriate reagents above each ar must be in the correct order to receive full credit. priate reagents above each arrow. The reagents A. HBr, ether B. Br2, CH2Cl2 C. Br2, H2O D. 1. Hg(OAC)2, H2O/THF 2. NaBH4 E. 1. BH3, THF 2. H2O2, OH F. H2SO4, H2O/HgSO4 G. NBS, hy H. H/Pd/C...
7-9 please!
4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
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