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4 7. One of the following is much more acidic than the other. Circle...
7. One of the following is much more acidic than the other. Circle the more acidic...
7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) Acidity of one pf the it's shown 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 for the intermediate (4 pts) Br...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as either a 1,2 or 1,4 addition product. b. Write either "thermodynamic" or "kinetic" underneath each one. c. Draw the two resonance structures for the intermediate from which both form H-Br ton nroducts for the following reaction. Draw the the major product or products for the following reaction. Drow the resonance structures for the intermediate from which both form Bra/ hv NBS/ peroxides 11. Give...
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
Please show all work for Number 5: CH3OH and number 3, HF one. Thank you Complete...
Please show all work for
Number 5: CH3OH and number 3, HF one. Thank you
Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction...
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction below: (draw curved arrows, intermediates, and resonance structures if necessary. NO NEED FOR TRANSITION STATES! CH CH CH CH Br Heat CH,CH,OH OCH.CH Mechanism.14 points) Mechanism 2 points) Mechanism.3 14 points) 5. [14 pts] Provide the major products of reacting the alkene shown in the middle of the scheme below with all the reagents independently. Draw the products' structures in the corresponding table below...
6. (4 pts.) Draw the two resonance structures of the enolate formed from the following reaction: 7. (4 pts) Draw th...
6. (4 pts.) Draw the two resonance structures of the enolate formed from the following reaction: 7. (4 pts) Draw the structure of an alkyl bromide (R-Br) and an alkoxide (R-O) that would provide the most efficient synthesis of the following ether by the Williamson ether synthesis. Target ether 8. (5 pts.) Draw a mechanism for the following E2 reaction. Draw the major product. Be sure to include any necessary H's in your structure as you draw the mechanism. OH...
4. Reaction Fill-ins! Prediet the product(s) OR starting material of the following reactions. Remember, Hydride shifts...
4. Reaction Fill-ins! Prediet the product(s) OR starting material of the following reactions. Remember, Hydride shifts are possible ifwhen a more stable carbocation can exist (depending on reaction mechanism)! Put your answers in the indicated boxes H,SO, (cat), H,о а. 1,2-product 1,4-product Br Br HBr b. Br Minor produt Major product Minor product HCI C. 1,2-product 14-product HI Он MAJOR prod. Minor prod e. Draw the FULL electron-pushing mechanism for the reaction in part a above. INCLUDING ALL resonance contributors....
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...
I need question 5 answered 4. The pk, of our product is- 2-3 units lower than...
I need question 5 answered
4. The pk, of our product is- 2-3 units lower than the pK, of phenol. Two of seven resonance forms are shown. There are five additional resonance forms that are not shown. Those additional forms have the negative charge on a different atom than the one shown on the structures below. On one of resonance contributors shown, circle the other five atoms in the structure that will have a partial negative charge as a result...
with one another? no loan pais 1. For each compound shown below, number the illustrated protons...
with one another? no loan pais 1. For each compound shown below, number the illustrated protons according to their acidity: most acidic (1) to least acidic (3). (9 points) H H NH2 H OH HO F F OH O HS OH 13. Shown below is the formal structure of the amino acid methionine and its structure as it exists at physiological pH ( 7.3). In each case, the molecule itself is neutral; however at pH 7.3 there is an atom...
7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) Acidity of one pf the it's shown 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 for the intermediate (4 pts) Br...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as either a 1,2 or 1,4 addition product. b. Write either "thermodynamic" or "kinetic" underneath each one. c. Draw the two resonance structures for the intermediate from which both form H-Br ton nroducts for the following reaction. Draw the the major product or products for the following reaction. Drow the resonance structures for the intermediate from which both form Bra/ hv NBS/ peroxides 11. Give...
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
Please show all work for
Number 5: CH3OH and number 3, HF one. Thank you
Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction below: (draw curved arrows, intermediates, and resonance structures if necessary. NO NEED FOR TRANSITION STATES! CH CH CH CH Br Heat CH,CH,OH OCH.CH Mechanism.14 points) Mechanism 2 points) Mechanism.3 14 points) 5. [14 pts] Provide the major products of reacting the alkene shown in the middle of the scheme below with all the reagents independently. Draw the products' structures in the corresponding table below...
6. (4 pts.) Draw the two resonance structures of the enolate formed from the following reaction: 7. (4 pts) Draw the structure of an alkyl bromide (R-Br) and an alkoxide (R-O) that would provide the most efficient synthesis of the following ether by the Williamson ether synthesis. Target ether 8. (5 pts.) Draw a mechanism for the following E2 reaction. Draw the major product. Be sure to include any necessary H's in your structure as you draw the mechanism. OH...
4. Reaction Fill-ins! Prediet the product(s) OR starting material of the following reactions. Remember, Hydride shifts are possible ifwhen a more stable carbocation can exist (depending on reaction mechanism)! Put your answers in the indicated boxes H,SO, (cat), H,о а. 1,2-product 1,4-product Br Br HBr b. Br Minor produt Major product Minor product HCI C. 1,2-product 14-product HI Он MAJOR prod. Minor prod e. Draw the FULL electron-pushing mechanism for the reaction in part a above. INCLUDING ALL resonance contributors....
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...
I need question 5 answered
4. The pk, of our product is- 2-3 units lower than the pK, of phenol. Two of seven resonance forms are shown. There are five additional resonance forms that are not shown. Those additional forms have the negative charge on a different atom than the one shown on the structures below. On one of resonance contributors shown, circle the other five atoms in the structure that will have a partial negative charge as a result...
with one another? no loan pais 1. For each compound shown below, number the illustrated protons according to their acidity: most acidic (1) to least acidic (3). (9 points) H H NH2 H OH HO F F OH O HS OH 13. Shown below is the formal structure of the amino acid methionine and its structure as it exists at physiological pH ( 7.3). In each case, the molecule itself is neutral; however at pH 7.3 there is an atom...
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