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Question 10. Using arrows to indicate the flow of electrons, provide a step-by-step mechanism which relates...
please help solve this Question 10. Using arrows to indicate the flow of electrons, provide a step-by-step mechanis...
please help solve this
Question 10. Using arrows to indicate the flow of electrons, provide a step-by-step mechanism which relates the starting materials to the products. Messy or incoherent answers will result in reduced or zero credit. Clearly cross out or remove anything you do not wish graded. All protonations/deprotonations must be explicitly shown; use of "proton transfer or P.T." is not permitted, and will receive zero credit if used in error. Clearly indicate formal charges if applicable. a)H,50 (cat.),...
please solve these questions thank you so much For questions 1-9, select the reaction conditions (A-1)...
please solve these questions
thank you so much
For questions 1-9, select the reaction conditions (A-1) which would create the major organic product(s) in the number of steps permitted in each box. a) H,50, (cat.), NH, b) workup a) Cro ,H, SOX, H,0 (Jones Reagent) b) workup a) H.SO(cat.), CH,OH b) workup a) H,50,(cat.),(CH), NH b) workup a) NaBH, CH,OH b) H20-workup a) Croy, pyridine, HCl, solvent (PCC) b) workup a) H, 50, (cat.), CH,CH,OH b) workup a)H,SO, (cat.), CH...
please show all the arrows ethylamine does not provide any product (1). However, when Ill is...
please show all the arrows
ethylamine does not provide any product (1). However, when Ill is exposed to identical conditions, product IV is isolated as the major organic product. Using arrows to indicate the flow of electrons, explain the formation of IV from III by providing a step-by-step mechanism. Messy or incoherent steps/structures will receive reduced or zero credit. Clearly indicate formal charges and stereochemistry if applicable. a) excess CH, NH, solvent TOH b)H,0* - workup IL H This product...
clearer images For questions 1 - 5. predict the major organic products for the following transformations....
clearer images
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. OH 1. a) Croy, H,SO,,H,O (Jones reagent) b) workup 2. a) HCI (cat.), CH, OH b) workup Q2 1. a) Croy, pyridine, HCl, solvent (PCC) b) workup 2. a) HCI (cat.), CH, OH b) workup a) NaOH, solvent,...
please help solve For questions 1 - 5. predict the major organic products for the following...
please help solve
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. CHO a) Nah, solvent b) workup a) LDA, solvent b) CH, Br, solvent c) workup a) Nah, solvent b) CH, Br, solvent c) workup CHO a) NaOH,H,O, HEAT b) workup a)excess NaOCH, CH, OH b)1,4-dibromobutane, solvent c)...
please help solve this
Question 10. Using arrows to indicate the flow of electrons, provide a step-by-step mechanism which relates the starting materials to the products. Messy or incoherent answers will result in reduced or zero credit. Clearly cross out or remove anything you do not wish graded. All protonations/deprotonations must be explicitly shown; use of "proton transfer or P.T." is not permitted, and will receive zero credit if used in error. Clearly indicate formal charges if applicable. a)H,50 (cat.),...
please solve these questions
thank you so much
For questions 1-9, select the reaction conditions (A-1) which would create the major organic product(s) in the number of steps permitted in each box. a) H,50, (cat.), NH, b) workup a) Cro ,H, SOX, H,0 (Jones Reagent) b) workup a) H.SO(cat.), CH,OH b) workup a) H,50,(cat.),(CH), NH b) workup a) NaBH, CH,OH b) H20-workup a) Croy, pyridine, HCl, solvent (PCC) b) workup a) H, 50, (cat.), CH,CH,OH b) workup a)H,SO, (cat.), CH...
please show all the arrows
ethylamine does not provide any product (1). However, when Ill is exposed to identical conditions, product IV is isolated as the major organic product. Using arrows to indicate the flow of electrons, explain the formation of IV from III by providing a step-by-step mechanism. Messy or incoherent steps/structures will receive reduced or zero credit. Clearly indicate formal charges and stereochemistry if applicable. a) excess CH, NH, solvent TOH b)H,0* - workup IL H This product...
clearer images
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. OH 1. a) Croy, H,SO,,H,O (Jones reagent) b) workup 2. a) HCI (cat.), CH, OH b) workup Q2 1. a) Croy, pyridine, HCl, solvent (PCC) b) workup 2. a) HCI (cat.), CH, OH b) workup a) NaOH, solvent,...
please help solve
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. CHO a) Nah, solvent b) workup a) LDA, solvent b) CH, Br, solvent c) workup a) Nah, solvent b) CH, Br, solvent c) workup CHO a) NaOH,H,O, HEAT b) workup a)excess NaOCH, CH, OH b)1,4-dibromobutane, solvent c)...
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