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Please answer Q2. Will upvote, guaranteed. Thank you and much appreciation. A) Draw the complete mechanism...
Pleaes answer a1a, b, and c. Will upvote, guaranteed. Thank you and much appreciation. Full reaction...
Pleaes answer a1a, b, and c. Will upvote, guaranteed. Thank you and much appreciation. Full reaction Q1a) Based on the reaction above, complete the following step: CI Full reaction 0 1) Excess LAH 2)H2O + CH,OH a1b) Based on the reaction above, complete the following step CH Full reaction 1) Excesa MaMgBr 2) H2O a1c) Based on the reaction above, complete the following step: 0
Could someone answer this correctly for me please, explaining the mechanism. Thank you. 22) Write a...
Could someone answer this correctly for me please, explaining
the mechanism. Thank you.
22) Write a detailed, stepwise mechanism to show formation of the major product from the reaction conditions shown below (this means draw the curved arrows). br sh BONUS (1 point): name the starting material following IUPAC nomenclature.
Provide the product of this reaction and draw a detailed step-by-step mechanism. Make sure to use...
Provide the product of this reaction and draw a detailed
step-by-step mechanism. Make sure to use the curved arrows
correctly and indicate all relevant unshared electron pairs and all
formal charges.
Thank you!
o cat. H20+ НО, MgSO4 anhydrous OH
Consider the mechanism for the following reaction: Tip: Before answering the question, draw a complete, detailed...
Consider the mechanism for the following reaction: Tip: Before answering the question, draw a complete, detailed mechanism for this reaction on a piece of paper. Use appropriate curved arrows to indicate the direction of electron flow and show the structures of all intermediates. The structures of transition states are NOT required. MeOH Br NH2 MeOH, HN Which of the following would be an intermediate on the path leading to the final product shown? A) Br M aHego HN E) PerwNH...
Complete the mechanism of the following Diels-Alder reaction by drawing the curved arrows for the concerted...
Complete the mechanism of the following Diels-Alder reaction by drawing the curved arrows for the concerted reaction and the final product formed. (Note that the COOH group is a carboxylic acid group, which is electron withdrawing.) Interactive 3D display mode Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the grid and connecting them with bonds, including charges where needed. Indicate the mechanism by drawing the electron-flow arrows on the molecules. Arrows should start on...
please help! thank you 47) Draw out the reaction mechanism for a Fischer esterification reaction with...
please help! thank you
47) Draw out the reaction mechanism for a Fischer esterification reaction with ethanol and benzoic acid in hot acidic conditions. Name the products. 48) Draw out the reaction mechanism for a Fischer esterification reaction when 5-hydroxyhexanoic acid is heated. Name the products if you feel ambitious.
3. Show the complete mechanism for the following nucleophilic aromatic substitution reaction. Use curved arrows to...
3. Show the complete mechanism for the following nucleophilic aromatic substitution reaction. Use curved arrows to indicate the direction of electron flow. Cl OH KOH + KCI NE 0
Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with...
Draw the complete electron-pushing mechanism for each of the
reactions. Please draw the reactants, intermediates (with formal
charges), products, and electron-pushing arrows.
1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 OH H2O HCI
HOMEWORK 4-CARBOXYLIC AICD AND ESTER, DUE TO APRIL. 18, 2018 (PLEASE STAPLE YOUR HOMEWORK) 3. Write...
HOMEWORK 4-CARBOXYLIC AICD AND ESTER, DUE TO APRIL. 18, 2018 (PLEASE STAPLE YOUR HOMEWORK) 3. Write the complete stepwise mechanism for this reaction. Show intermediate structures and all electron flow with arrows. OEt NaH OH 4. Consider the information below to answer the following question(s). The reaction of a carboxylic acid with an alcohol in the presence of acid is termed Fischer esterification The nucleophile in this reaction is The function of C is a Write the stepwise mechanism for...
please answer completely and clearly. thank you! SHORT ANSWER #28: Draw a full mechanism for the...
please answer completely and clearly. thank you!
SHORT ANSWER #28: Draw a full mechanism for the following transformation Aldol condensation reaction and predict the product. Show all the elementary step(s) being sure to include all arrows, important electron pairs and any formal charges if needed. (8 points) NaOH, HAO heat Aldol condensation product H
Pleaes answer a1a, b, and c. Will upvote, guaranteed. Thank you and much appreciation. Full reaction Q1a) Based on the reaction above, complete the following step: CI Full reaction 0 1) Excess LAH 2)H2O + CH,OH a1b) Based on the reaction above, complete the following step CH Full reaction 1) Excesa MaMgBr 2) H2O a1c) Based on the reaction above, complete the following step: 0
Could someone answer this correctly for me please, explaining
the mechanism. Thank you.
22) Write a detailed, stepwise mechanism to show formation of the major product from the reaction conditions shown below (this means draw the curved arrows). br sh BONUS (1 point): name the starting material following IUPAC nomenclature.
Provide the product of this reaction and draw a detailed
step-by-step mechanism. Make sure to use the curved arrows
correctly and indicate all relevant unshared electron pairs and all
formal charges.
Thank you!
o cat. H20+ НО, MgSO4 anhydrous OH
Consider the mechanism for the following reaction: Tip: Before answering the question, draw a complete, detailed mechanism for this reaction on a piece of paper. Use appropriate curved arrows to indicate the direction of electron flow and show the structures of all intermediates. The structures of transition states are NOT required. MeOH Br NH2 MeOH, HN Which of the following would be an intermediate on the path leading to the final product shown? A) Br M aHego HN E) PerwNH...
please help! thank you
47) Draw out the reaction mechanism for a Fischer esterification reaction with ethanol and benzoic acid in hot acidic conditions. Name the products. 48) Draw out the reaction mechanism for a Fischer esterification reaction when 5-hydroxyhexanoic acid is heated. Name the products if you feel ambitious.
3. Show the complete mechanism for the following nucleophilic aromatic substitution reaction. Use curved arrows to indicate the direction of electron flow. Cl OH KOH + KCI NE 0
Draw the complete electron-pushing mechanism for each of the
reactions. Please draw the reactants, intermediates (with formal
charges), products, and electron-pushing arrows.
1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 OH H2O HCI
HOMEWORK 4-CARBOXYLIC AICD AND ESTER, DUE TO APRIL. 18, 2018 (PLEASE STAPLE YOUR HOMEWORK) 3. Write the complete stepwise mechanism for this reaction. Show intermediate structures and all electron flow with arrows. OEt NaH OH 4. Consider the information below to answer the following question(s). The reaction of a carboxylic acid with an alcohol in the presence of acid is termed Fischer esterification The nucleophile in this reaction is The function of C is a Write the stepwise mechanism for...
please answer completely and clearly. thank you!
SHORT ANSWER #28: Draw a full mechanism for the following transformation Aldol condensation reaction and predict the product. Show all the elementary step(s) being sure to include all arrows, important electron pairs and any formal charges if needed. (8 points) NaOH, HAO heat Aldol condensation product H
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