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Complete the reaction scheme. Complete structures are required; If a reagent has a common abbreviation, then...
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then...
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 2a. Predict the product 2 equivalents toillot -NH: excess + 2 HNET 8
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then...
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 1a. Predict the product 1) KHMDS, -78 °C 2) Que H OCH, 3) H,0* (workup) 8
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then...
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 15. The Robinson Annulation combines two reactions to form a cyclica.B-unsaturated ketone. Provide the dicarbonyl intermediate and the final product. You do not need to worry about stereochemistry 15a. Draw the expected intermediate son OH (solvent) 10 15b. Predict the product. 10
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then...
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 8a. Provide the starting compound. Intramolecular Diels-Alder 10
Complete the reaction scheme. Complete structures are required; If a reagent has a common abbreviation, then...
Complete the reaction scheme. Complete structures are required; If a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 9a. Predict the product. No stereochemistry needs to be shown TsOH носн, + H₂O 8 9b. What is the expected stereochemical outcome? a single chiral compound a racemic mixture circle one: a pair of 2 diastereomers a mixture of 3 or more stereoisomers 6
Complete the reaction scheme. Complete structures are required; If a reagent has a common abbreviation, then...
Complete the reaction scheme. Complete structures are required; If a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 5. The nitroso group (NO) is a versatile functional group that activates benzene in electrophilic aromatic substitution reactions. For the follow reaction, draw the best structure for the intermediate and then provide the product as well. 5a. Draw the best structure of the expected intermediate....
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then...
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 13. The Colorado potato beetle is a worldwide pest. A male-produced aggression pheromone was identified and proved practical in pest management and organic farming. Complete the reaction scheme as requested in the pheromone synthesis. 13a. Provide the reagent(s). 13b. Provide the reagent(s). OH 8 5...
V. (20 points) Complete the reaction scheme. Complete structures are required; if a reagent has a...
V. (20 points) Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 5a. Predict the product. No stereochemistry needs to be shown 1) LDA (2 eq) H30+ Heat 3) H2O+ 5b. How many stereoisomers of the product would be formed? 5d. Predict the product. 5c. Predict the product. K2CO3 + CO2 + HOCH2CH3 5
Fill in the blank with the correct product or reagent to complete the reaction. Hz, Pd/C...
Fill in the blank with the correct product or reagent to
complete the reaction.
Hz, Pd/C NO2 OH POCI. pyridine OCH3 OCH3
Complete the following sequence by filling in missing reagents or providing the product(s) of a reaction....
Complete the following sequence by filling in missing reagents or providing the product(s) of a reaction. Sequential steps, if necessary, should be numbered. How Toot OH OMs major product minor product
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 2a. Predict the product 2 equivalents toillot -NH: excess + 2 HNET 8
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 1a. Predict the product 1) KHMDS, -78 °C 2) Que H OCH, 3) H,0* (workup) 8
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 15. The Robinson Annulation combines two reactions to form a cyclica.B-unsaturated ketone. Provide the dicarbonyl intermediate and the final product. You do not need to worry about stereochemistry 15a. Draw the expected intermediate son OH (solvent) 10 15b. Predict the product. 10
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 8a. Provide the starting compound. Intramolecular Diels-Alder 10
Complete the reaction scheme. Complete structures are required; If a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 9a. Predict the product. No stereochemistry needs to be shown TsOH носн, + H₂O 8 9b. What is the expected stereochemical outcome? a single chiral compound a racemic mixture circle one: a pair of 2 diastereomers a mixture of 3 or more stereoisomers 6
Complete the reaction scheme. Complete structures are required; If a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 5. The nitroso group (NO) is a versatile functional group that activates benzene in electrophilic aromatic substitution reactions. For the follow reaction, draw the best structure for the intermediate and then provide the product as well. 5a. Draw the best structure of the expected intermediate....
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 13. The Colorado potato beetle is a worldwide pest. A male-produced aggression pheromone was identified and proved practical in pest management and organic farming. Complete the reaction scheme as requested in the pheromone synthesis. 13a. Provide the reagent(s). 13b. Provide the reagent(s). OH 8 5...
V. (20 points) Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 5a. Predict the product. No stereochemistry needs to be shown 1) LDA (2 eq) H30+ Heat 3) H2O+ 5b. How many stereoisomers of the product would be formed? 5d. Predict the product. 5c. Predict the product. K2CO3 + CO2 + HOCH2CH3 5
Fill in the blank with the correct product or reagent to
complete the reaction.
Hz, Pd/C NO2 OH POCI. pyridine OCH3 OCH3
Complete the following sequence by filling in missing reagents or providing the product(s) of a reaction. Sequential steps, if necessary, should be numbered. How Toot OH OMs major product minor product
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