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Draw the mechanism for the sulfonation of benzene. Use HSO3 as the electrophile. Draw the all...
Application Questions 1.Draw the mechanism for the sulfonation of benzene. Use HSO3+as the electrophile. Draw the...
Application Questions 1.Draw the mechanism for the sulfonation of benzene. Use HSO3+as the electrophile. Draw the all the resonance structures of the stabilized cation intermediate
all three questions Application Questions 1. Draw the mechanism for the sulfonation of benzene. Use HSO...
all three questions
Application Questions 1. Draw the mechanism for the sulfonation of benzene. Use HSO as the electrophile. Draw the all the resonance structures of the stabilized cation intermediate 2. Draw the major product formed when each of the following compounds is treated with Cly/AICI, Assume chlorination only occurs in one position on the ring rather than multiple positions. COM COCX ooo 3. Predict whether toluene or chlorobenzene would undergo electrophilic aromatic substitution more quickly when treated with C1z/AICI....
9) Identify the electrophile in the sulfonation reaction of benzene. 2 Pt A. SO2 B. H2SO4...
9) Identify the electrophile in the sulfonation reaction of benzene. 2 Pt A. SO2 B. H2SO4 C. Sos* D. H2SO3 E. SO3 10) Write the mechanism for the following EAS reaction? 4 Pt CI. AICI 11) Predict the all possible products for the following reactions and circle the major product among them? 8 Pt olub HNO3. H,SO A) Yo Cl2, AICI: B) CH,CI, AICI: Сн, HNO3, H2SO4 D) OH
5. When benzamide (the reactant shown) is treated with the acylium cation electrophile shown (generated by...
5. When benzamide (the reactant shown) is treated with the acylium cation electrophile shown (generated by combining concentrated acetyl chloride and aluminum trichloride), the first step of the reaction involves the benzene ring attacking the carbocation to form a sigma complex intermediate. (This curved arrows have been included in the reaction below.) Draw the sigma complex intermediate (including all resonance structures) resulting from meta attack (acyl group adds to meta carbon) and para attack (acyl group adds to para carbon)...
all H₃C CHECH₂ (b). Question 5. For the following reaction mechanism of benzene sulfonation, add missing...
all
H₃C CHECH₂ (b). Question 5. For the following reaction mechanism of benzene sulfonation, add missing Lone pair electrons and curved arrow to show the formation of the intermediates and final product. Identify the pattern of the reaction mechanism in each step Question 6. For the structures shown, indicate whether the two species are constitutional isomers, enantiomers, diastereomers of one another, or identical molecules. | H CH(CH3)2 –COOH | HẠN CH(CH3)2 COOH
Draw the mechanism of the following reaction. Be sure to show all curved arrows and formal...
Draw the mechanism of the following reaction. Be sure to show all curved arrows and formal charges. (Show the formation of the electrophile and all resonance structures of the sigma complex). o to AICI: Does the substituent on the following benzene activate or deactivate the ring for EAS reactions? Explain your answer this should include drawing any relevant resonance structures!) NH Predict the major product of the following reaction. Explain the directing effects of the -OH group (this should include...
Use resonance forms to show that the dipolar sigma complex shown in the sulfonation of benzene...
Use resonance forms to show that the dipolar sigma complex shown in the sulfonation of benzene has its positive charge delocalized over three carbon atoms and its negative charge delocalized over three oxygen atoms. Draw the molecule on the canvas y choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. H H Br Marvin JS A OO Od Request Answer Submit
6. Predict the product and draw a mechanism for the reactions below. You MUST include the...
6. Predict the product and draw a mechanism for the reactions below. You MUST include the mechanism for the formation of the electrophile. Be sure to show arrows for every bond change and draw the resonance structures of the carbocation intermediate. AICI: SO3 H2SO4
are these correct? if not, can you explain? thanks! 9. a) Draw the mechanism for formation...
are these correct? if not, can
you explain? thanks!
9. a) Draw the mechanism for formation of the product shown. b) Draw the three resonance structures for the cation intermediate. (6 points total) HO-NO2 H2SO4 NO2 A mechanism: H-O-NO2 + H₂SO4 a H-O No2 t B) Resonance structures H NO2 H NO₂
help with all of them please 1) Complete the following reactions OH H2SO4 (a) (b) OH...
help with all of them please
1) Complete the following reactions OH H2SO4 (a) (b) OH H2SO4 (c) H2SO4 heat heat OH heat ОН H.CO d) HỌCrO, H2C104 e) -OH OH 2) Show how to convert (a) 1-Propanol to 2-propanol in two steps (b) Cyclohexene to cyclohexanone in two steps (c) Propene to propanone (acetone) in two steps. 3) Write a stepwise mechanism for the sulfonation of benzene. Use HSO3 + as the electrophile.
all three questions
Application Questions 1. Draw the mechanism for the sulfonation of benzene. Use HSO as the electrophile. Draw the all the resonance structures of the stabilized cation intermediate 2. Draw the major product formed when each of the following compounds is treated with Cly/AICI, Assume chlorination only occurs in one position on the ring rather than multiple positions. COM COCX ooo 3. Predict whether toluene or chlorobenzene would undergo electrophilic aromatic substitution more quickly when treated with C1z/AICI....
9) Identify the electrophile in the sulfonation reaction of benzene. 2 Pt A. SO2 B. H2SO4 C. Sos* D. H2SO3 E. SO3 10) Write the mechanism for the following EAS reaction? 4 Pt CI. AICI 11) Predict the all possible products for the following reactions and circle the major product among them? 8 Pt olub HNO3. H,SO A) Yo Cl2, AICI: B) CH,CI, AICI: Сн, HNO3, H2SO4 D) OH
5. When benzamide (the reactant shown) is treated with the acylium cation electrophile shown (generated by combining concentrated acetyl chloride and aluminum trichloride), the first step of the reaction involves the benzene ring attacking the carbocation to form a sigma complex intermediate. (This curved arrows have been included in the reaction below.) Draw the sigma complex intermediate (including all resonance structures) resulting from meta attack (acyl group adds to meta carbon) and para attack (acyl group adds to para carbon)...
all
H₃C CHECH₂ (b). Question 5. For the following reaction mechanism of benzene sulfonation, add missing Lone pair electrons and curved arrow to show the formation of the intermediates and final product. Identify the pattern of the reaction mechanism in each step Question 6. For the structures shown, indicate whether the two species are constitutional isomers, enantiomers, diastereomers of one another, or identical molecules. | H CH(CH3)2 –COOH | HẠN CH(CH3)2 COOH
Draw the mechanism of the following reaction. Be sure to show all curved arrows and formal charges. (Show the formation of the electrophile and all resonance structures of the sigma complex). o to AICI: Does the substituent on the following benzene activate or deactivate the ring for EAS reactions? Explain your answer this should include drawing any relevant resonance structures!) NH Predict the major product of the following reaction. Explain the directing effects of the -OH group (this should include...
Use resonance forms to show that the dipolar sigma complex shown in the sulfonation of benzene has its positive charge delocalized over three carbon atoms and its negative charge delocalized over three oxygen atoms. Draw the molecule on the canvas y choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. H H Br Marvin JS A OO Od Request Answer Submit
6. Predict the product and draw a mechanism for the reactions below. You MUST include the mechanism for the formation of the electrophile. Be sure to show arrows for every bond change and draw the resonance structures of the carbocation intermediate. AICI: SO3 H2SO4
are these correct? if not, can
you explain? thanks!
9. a) Draw the mechanism for formation of the product shown. b) Draw the three resonance structures for the cation intermediate. (6 points total) HO-NO2 H2SO4 NO2 A mechanism: H-O-NO2 + H₂SO4 a H-O No2 t B) Resonance structures H NO2 H NO₂
help with all of them please
1) Complete the following reactions OH H2SO4 (a) (b) OH H2SO4 (c) H2SO4 heat heat OH heat ОН H.CO d) HỌCrO, H2C104 e) -OH OH 2) Show how to convert (a) 1-Propanol to 2-propanol in two steps (b) Cyclohexene to cyclohexanone in two steps (c) Propene to propanone (acetone) in two steps. 3) Write a stepwise mechanism for the sulfonation of benzene. Use HSO3 + as the electrophile.
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