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3. Draw the needed alcohol and reactants to prepare the shown products. Be sure to include...
NMR help 4a.Determine the structure of the unknown alcohol using the given 1H NMR. (5 points)...
NMR help
4a.Determine the structure of the unknown alcohol using the given 1H NMR. (5 points) 4b. Write the equation for the reaction of the above alcohol with HBr. (4 points) 4c. Draw the mechanism of this reaction (4 points)
4. Draw a mechanism for the following reactions: Be sure to include all products and stereochemistry...
4. Draw a mechanism for the following reactions: Be sure to include all products and stereochemistry when applicable. (8 pts each) H2SO4 HgSO4 to HC
help please! 18. Predict the reactants necessary to complete each reaction below. Be sure to include...
help please!
18. Predict the reactants necessary to complete each reaction below. Be sure to include all necessary reaction conditions (3 points each) 19. Given the current global epidemic involving the novel strain of coronavirus, COVID-19, the synthesis of anti-viral medications become increasingly more important. Provide the mechanism of the reaction below and discuss the observed regioselectivity. (6 points) HOMCO2Et CO2Et Но" Т TsOH 0 20. Unknown X is an acyclic 6-carbon alkane containing an alcohol with formula C6H13Bro. Treatment...
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...
What is the splitting and integration for the protons indicated below? triplet, 2H multiplet (5), 1H...
What is the splitting and integration for the protons indicated below? triplet, 2H multiplet (5), 1H singlet, 1H doublet, 1H triplet, 1H NH2 OOO The integration on a 'H NMR spectra containing three peaks is as follows for a molecule with the molecular formula C6H12O; A = 18, B = 12, and C = 6.0. How many hydrogens does peak B represent? OB = 12 B = 2 B = 6 B = 6.0 B=4 Draw the structure for 2,4Z-2-bromo-4-ethyl-2,4-hexandiene....
3. There are two possible substitution products fr products and a complete mechanism for their for...
3. There are two possible substitution products fr products and a complete mechanism for their for IUPAC system and circle the major product. Ustitution products from the reaction of 3,3-dimethyl-2-butanol with aq. HBr. Draw the mechanism for their formation, including all intermediates. Name both products based on the :OH MW: 102. Ts-gimo 4. Based on the reaction above, calculate the theoretical yield for the reaction based on 2.0 g of the 3,3-dimethyl-2- butanol and 5 mL of the 48% HBr....
1. Provide the products for the following reactions (1 points). NaOH, Ethanol 2. Draw the mechanism...
1. Provide the products for the following reactions (1 points). NaOH, Ethanol 2. Draw the mechanism for the reaction above (2 points). 3. Draw the 1H-NMR for the structure below. Label each peak on the NMR (2 points): DE H CE
3. . Draw all the possible resonance structures: (6 points) 4. Write the products or reactants:...
3. . Draw all the possible resonance
structures: (6 points)
4. Write the products or reactants: (12
points)
3.. Draw all the possible resonance structures: (6 points) OCH3 H NO2 a. CH2 CH + H3C CH2 b. H,C 4. Write the products or reactants: (12 points) COOH 0-1 heat COOH a. HBr, leq b.
1. Provide the products for the following reactions (1 points). NaOH, Ethanol н 2. Draw the...
1. Provide the products for the following reactions (1 points). NaOH, Ethanol н 2. Draw the mechanism for the reaction above (2 points). 3. Draw the 1H-NMR for the structure below. Label each peak on the NMR (2 points): G AM O 5 0
products of alcohol reduction reactions? Draw the structure of the final product expected for each of...
products of alcohol reduction reactions?
Draw the structure of the final product expected for each of the following reactions: be sure to accurately depict stereochemistry, where relevant, and if no reaction can occur, indicate by writing NR.
NMR help
4a.Determine the structure of the unknown alcohol using the given 1H NMR. (5 points) 4b. Write the equation for the reaction of the above alcohol with HBr. (4 points) 4c. Draw the mechanism of this reaction (4 points)
4. Draw a mechanism for the following reactions: Be sure to include all products and stereochemistry when applicable. (8 pts each) H2SO4 HgSO4 to HC
help please!
18. Predict the reactants necessary to complete each reaction below. Be sure to include all necessary reaction conditions (3 points each) 19. Given the current global epidemic involving the novel strain of coronavirus, COVID-19, the synthesis of anti-viral medications become increasingly more important. Provide the mechanism of the reaction below and discuss the observed regioselectivity. (6 points) HOMCO2Et CO2Et Но" Т TsOH 0 20. Unknown X is an acyclic 6-carbon alkane containing an alcohol with formula C6H13Bro. Treatment...
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...
What is the splitting and integration for the protons indicated below? triplet, 2H multiplet (5), 1H singlet, 1H doublet, 1H triplet, 1H NH2 OOO The integration on a 'H NMR spectra containing three peaks is as follows for a molecule with the molecular formula C6H12O; A = 18, B = 12, and C = 6.0. How many hydrogens does peak B represent? OB = 12 B = 2 B = 6 B = 6.0 B=4 Draw the structure for 2,4Z-2-bromo-4-ethyl-2,4-hexandiene....
3. There are two possible substitution products fr products and a complete mechanism for their for IUPAC system and circle the major product. Ustitution products from the reaction of 3,3-dimethyl-2-butanol with aq. HBr. Draw the mechanism for their formation, including all intermediates. Name both products based on the :OH MW: 102. Ts-gimo 4. Based on the reaction above, calculate the theoretical yield for the reaction based on 2.0 g of the 3,3-dimethyl-2- butanol and 5 mL of the 48% HBr....
1. Provide the products for the following reactions (1 points). NaOH, Ethanol 2. Draw the mechanism for the reaction above (2 points). 3. Draw the 1H-NMR for the structure below. Label each peak on the NMR (2 points): DE H CE
3. . Draw all the possible resonance
structures: (6 points)
4. Write the products or reactants: (12
points)
3.. Draw all the possible resonance structures: (6 points) OCH3 H NO2 a. CH2 CH + H3C CH2 b. H,C 4. Write the products or reactants: (12 points) COOH 0-1 heat COOH a. HBr, leq b.
1. Provide the products for the following reactions (1 points). NaOH, Ethanol н 2. Draw the mechanism for the reaction above (2 points). 3. Draw the 1H-NMR for the structure below. Label each peak on the NMR (2 points): G AM O 5 0
products of alcohol reduction reactions?
Draw the structure of the final product expected for each of the following reactions: be sure to accurately depict stereochemistry, where relevant, and if no reaction can occur, indicate by writing NR.
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