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For questions 1-9, select the reaction conditions (A-1)...
clearer images For questions 1 - 5. predict the major organic products for the following transformations....
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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 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.),...
Question 10. Using arrows to indicate the flow of electrons, provide a step-by-step mechanism which relates...
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) H2SO4 (cat.), H20 e non...
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 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...
how is the reaction step, detailed steps, thanks. Question 35 OCH a) H,50(cat.), H,0 H₃co e...
how
is the reaction step, detailed steps, thanks.
Question 35 OCH a) H,50(cat.), H,0 H₃co e + CH₃OH b) workup
"ОН Step 1 Fill in the following reaction scheme based on the Roman numerals provided below:...
"ОН Step 1 Fill in the following reaction scheme based on the Roman numerals provided below: но Η Ν. HO HOH НО-Н Step 2 H-OH H-OH H ОН HO -Η HO -H НО. H HOH HO -H HO+H CH, OH CH OH CH OH Step 3 HCN cat. HCI H,0 HIO NH,OH NaBHA EROH - 11 III IV V NaOCH, Bra H.0 VII cat HCI CH,OH но" Pa/Baso Hy XI VI VIII х HNO H.O heat XI H,02 Fox(50) XII...
Could you please help me with these questions. Thank you so much 6. Which of the...
Could you please help me with these questions. Thank you so much
6. Which of the following statements is NOT true of ethers? a. Ethers are generally unreactive molecules toward reagents other than strong acids. b. Ethers generally have lower boiling points than alcohols of a corresponding molecular weight. c. Ethers generally have much lower water solubilities than alcohols with a corresponding molecular weight. d. Ethers can generally be cleaved by heating them with strong acids e. Ethers form peroxides...
Thank you so much to anyone who decides to help me with this page. I am very grateful! 1. (4pts) How many signal...
Thank you so much to anyone who decides to help me
with this page. I am very grateful!
1. (4pts) How many signals do you expect each of the following compounds to have in its 'H NMR spectrum? Write the appropriate number below to each structure. OH OH H 2. (5.5pts) Use your spectrOscopy data table to identify the chemical shift range in which each of the identified signals in the folowing molecule wDuld be lournd in the 'H NMR...
please help! will give rating. thank you! L. 1.CH,Br 2. H,0 M. NaBH CH, OH 0....
please help! will give rating. thank you!
L. 1.CH,Br 2. H,0 M. NaBH CH, OH 0. Brz P. Hz, Pd N. 1. KCN 2. LIAIHA 3. H2O ОН Q. NaOH, Bra B. 1, KCN 2. HCI 3. cat NaOH H2O S. NHA mild H+ I. NH3 NaBH3CN U. 1. CHgMgBr 2. H2O, H Determine the reagents necessary to carry out each of the following transformations. The reagent choices are listed in the text box above this question (reagents L-U). You...
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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 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.),...
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) H2SO4 (cat.), H20 e non...
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 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...
how
is the reaction step, detailed steps, thanks.
Question 35 OCH a) H,50(cat.), H,0 H₃co e + CH₃OH b) workup
"ОН Step 1 Fill in the following reaction scheme based on the Roman numerals provided below: но Η Ν. HO HOH НО-Н Step 2 H-OH H-OH H ОН HO -Η HO -H НО. H HOH HO -H HO+H CH, OH CH OH CH OH Step 3 HCN cat. HCI H,0 HIO NH,OH NaBHA EROH - 11 III IV V NaOCH, Bra H.0 VII cat HCI CH,OH но" Pa/Baso Hy XI VI VIII х HNO H.O heat XI H,02 Fox(50) XII...
Could you please help me with these questions. Thank you so much
6. Which of the following statements is NOT true of ethers? a. Ethers are generally unreactive molecules toward reagents other than strong acids. b. Ethers generally have lower boiling points than alcohols of a corresponding molecular weight. c. Ethers generally have much lower water solubilities than alcohols with a corresponding molecular weight. d. Ethers can generally be cleaved by heating them with strong acids e. Ethers form peroxides...
Thank you so much to anyone who decides to help me
with this page. I am very grateful!
1. (4pts) How many signals do you expect each of the following compounds to have in its 'H NMR spectrum? Write the appropriate number below to each structure. OH OH H 2. (5.5pts) Use your spectrOscopy data table to identify the chemical shift range in which each of the identified signals in the folowing molecule wDuld be lournd in the 'H NMR...
please help! will give rating. thank you!
L. 1.CH,Br 2. H,0 M. NaBH CH, OH 0. Brz P. Hz, Pd N. 1. KCN 2. LIAIHA 3. H2O ОН Q. NaOH, Bra B. 1, KCN 2. HCI 3. cat NaOH H2O S. NHA mild H+ I. NH3 NaBH3CN U. 1. CHgMgBr 2. H2O, H Determine the reagents necessary to carry out each of the following transformations. The reagent choices are listed in the text box above this question (reagents L-U). You...
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