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03 Question (5 points) See page 407 A pair of diastereomers is each individually mixed with a strong base, and for...
i need steps 3,4,6 they are shown in order 23 Question points) See page 1062 Provide...
i need steps 3,4,6 they are shown in order
23 Question points) See page 1062 Provide the missing curved arrows and structures to complete the mechanism of the Fischer esterification. Your structures should include all nonzero formal charges and lone pairs of electrons. The reagents you need for each mechanistic step are provided in each box 29th attempt See Periodic Table See Hint best- Y". art um - -.* Add the missing curved arrow notation VIEW SOLUTION Add the missing...
i need steps 3.4,6 please 11. 20/19 23 Question See page 1062 points) Provide the missing...
i need steps 3.4,6 please
11. 20/19 23 Question See page 1062 points) Provide the missing curved arrows and structures to complete the mechanism of the Fischer esterification. Your structures should indude all nonzero formal charges and one pairs of electrons. The reagents you need for each mechanistic step are provided in each box. 29th attempt See Periodic Table See Hint op Draw the organic intermediate with lone pair electrons and non-zero formal charges. Add the curved arrow notation.
05 Question (2 points) @ See page 367 Complete the mechanism and select the correct frontier...
05 Question (2 points) @ See page 367 Complete the mechanism and select the correct frontier orbital interaction for the reaction. 4th attempt Part 1 (1 point) Complete the mechanism below by supplying the missing curved arrow notation. H- OH - H-ö—¢—H :C: I i Add the missing curved arrow notation. Do not add or remove structures or atoms.
just need help with step 5 27 Question (4 points) See page 1078 Draw a mechanism for the acetoacetic ester synthes...
just need help with step 5
27 Question (4 points) See page 1078 Draw a mechanism for the acetoacetic ester synthesis. On the existing structures, provide curved arrows. In the blank boxes, draw the required structure requested. Do not include by-products. 16th attempt See Periodic Table See Hint - - , notation to form the enolate via decarboxylation. Foll. < 27127 + VIEW SOLUTION
10 Question (3 points) @ See page 920 Complete the mechanism for the intramolecular aldol reaction...
10 Question (3 points) @ See page 920 Complete the mechanism for the intramolecular aldol reaction shown below. Add the missing curved arrow notation, lone pair electrons, and nonzero formal charges to all boxes. The reaction requires a base (e.g., NaOH) but we will ignore the Nat because it does not participate in the mechanism. Do not add any other reagents. :0— I Elcb Draw lone pairs, non-zero formal charges, and curved arrows to show how hydroxide reacts with the...
no attempt penalty 4 Question (1point) e See page 584 When 1,3-pentadiene is protonated, a resonance-stabilized sec...
no attempt penalty 4 Question (1point) e See page 584 When 1,3-pentadiene is protonated, a resonance-stabilized secondarry allylic carbocation is formed. Draw the curved arrow notation below that shows the movement of electrons between the two major resonance structures. 1st attempt Jed See Periodic Table See Hint Feedback C TRY AGAIN VIEW SOLUTION <04/12 1 OF 12 QUESTIONS COMPLETED MacBook Pro
See page 348 42 Question (5 points) Draw the curved arrow notation and products for the...
See page 348 42 Question (5 points) Draw the curved arrow notation and products for the each elementary step described by the sequence shown here. Note that the products of each step should be used as the reactants in the next step, and you may need to draw in additional reagents as directed. Remember to click on each box to see step-specific instructions. 1. E2 involving H,N ? 2. Electrophile addition of Br 3. Coordination of Br
PLEASE SHOW ALL WORK AND PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you! 06 Question (4 points) e See page 574 Comp...
PLEASE SHOW ALL WORK AND
PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you!
06 Question (4 points) e See page 574 Complete the mechanism. All necessary atoms and bonds (that is, those that are involved in the mechanism) are drawn in for you already; do not modify the structures by adding or removing any atoms. 1st attempt See Periodic Table See Hint Add the missing curved arrow notation. e See pa 09 Question (4 points) Predict the organic starting...
See page 665 17 Question 15 points) Draw an alkylbromide with proper stereochemistry that can be...
See page 665 17 Question 15 points) Draw an alkylbromide with proper stereochemistry that can be used to synthesize the given alkene as the exclusive product via an E2 reaction HCYCH 2nd attempt Feedback cht See Periodic Table See Hint Please draw all four bonds at chiral centers. < 1720 > + VIEW SOLUTION C TRY AGAIN Please draw all four bonds at chiral centers, Edit the structure below to be the precursor alkyl bromide to this alkene: C TRY...
this is just one problem! I will rate SOUL OT55 28 Question (1 point) @ See...
this is just one problem! I will rate
SOUL OT55 28 Question (1 point) @ See page 983 An alkyl halide with formula C6H13X with the following 1 H NMR and MS was treated with lithium dimethylcuprate (Me Culi). Predict the major organic product for the following reaction sequence. Be sure your answer accounts for stereochemistry and regiochemistry, wher appropriate. If multiple stereoisomers are formed, be sure to draw all products using appropriate wedges and dashes. (The numbers at the...
i need steps 3,4,6 they are shown in order
23 Question points) See page 1062 Provide the missing curved arrows and structures to complete the mechanism of the Fischer esterification. Your structures should include all nonzero formal charges and lone pairs of electrons. The reagents you need for each mechanistic step are provided in each box 29th attempt See Periodic Table See Hint best- Y". art um - -.* Add the missing curved arrow notation VIEW SOLUTION Add the missing...
i need steps 3.4,6 please
11. 20/19 23 Question See page 1062 points) Provide the missing curved arrows and structures to complete the mechanism of the Fischer esterification. Your structures should indude all nonzero formal charges and one pairs of electrons. The reagents you need for each mechanistic step are provided in each box. 29th attempt See Periodic Table See Hint op Draw the organic intermediate with lone pair electrons and non-zero formal charges. Add the curved arrow notation.
05 Question (2 points) @ See page 367 Complete the mechanism and select the correct frontier orbital interaction for the reaction. 4th attempt Part 1 (1 point) Complete the mechanism below by supplying the missing curved arrow notation. H- OH - H-ö—¢—H :C: I i Add the missing curved arrow notation. Do not add or remove structures or atoms.
just need help with step 5
27 Question (4 points) See page 1078 Draw a mechanism for the acetoacetic ester synthesis. On the existing structures, provide curved arrows. In the blank boxes, draw the required structure requested. Do not include by-products. 16th attempt See Periodic Table See Hint - - , notation to form the enolate via decarboxylation. Foll. < 27127 + VIEW SOLUTION
10 Question (3 points) @ See page 920 Complete the mechanism for the intramolecular aldol reaction shown below. Add the missing curved arrow notation, lone pair electrons, and nonzero formal charges to all boxes. The reaction requires a base (e.g., NaOH) but we will ignore the Nat because it does not participate in the mechanism. Do not add any other reagents. :0— I Elcb Draw lone pairs, non-zero formal charges, and curved arrows to show how hydroxide reacts with the...
no attempt penalty 4 Question (1point) e See page 584 When 1,3-pentadiene is protonated, a resonance-stabilized secondarry allylic carbocation is formed. Draw the curved arrow notation below that shows the movement of electrons between the two major resonance structures. 1st attempt Jed See Periodic Table See Hint Feedback C TRY AGAIN VIEW SOLUTION <04/12 1 OF 12 QUESTIONS COMPLETED MacBook Pro
See page 348 42 Question (5 points) Draw the curved arrow notation and products for the each elementary step described by the sequence shown here. Note that the products of each step should be used as the reactants in the next step, and you may need to draw in additional reagents as directed. Remember to click on each box to see step-specific instructions. 1. E2 involving H,N ? 2. Electrophile addition of Br 3. Coordination of Br
PLEASE SHOW ALL WORK AND
PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you!
06 Question (4 points) e See page 574 Complete the mechanism. All necessary atoms and bonds (that is, those that are involved in the mechanism) are drawn in for you already; do not modify the structures by adding or removing any atoms. 1st attempt See Periodic Table See Hint Add the missing curved arrow notation. e See pa 09 Question (4 points) Predict the organic starting...
See page 665 17 Question 15 points) Draw an alkylbromide with proper stereochemistry that can be used to synthesize the given alkene as the exclusive product via an E2 reaction HCYCH 2nd attempt Feedback cht See Periodic Table See Hint Please draw all four bonds at chiral centers. < 1720 > + VIEW SOLUTION C TRY AGAIN Please draw all four bonds at chiral centers, Edit the structure below to be the precursor alkyl bromide to this alkene: C TRY...
this is just one problem! I will rate
SOUL OT55 28 Question (1 point) @ See page 983 An alkyl halide with formula C6H13X with the following 1 H NMR and MS was treated with lithium dimethylcuprate (Me Culi). Predict the major organic product for the following reaction sequence. Be sure your answer accounts for stereochemistry and regiochemistry, wher appropriate. If multiple stereoisomers are formed, be sure to draw all products using appropriate wedges and dashes. (The numbers at the...
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