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2. Synthesis: Fill in the missing products in the synthesis process below. Stereochemistry should be shown...
Predicting Products: Draw the structure of the one major organic product of each reaction in the...
Predicting Products: Draw the structure of the one major organic product of each reaction in the boxes provided. Be aware that the products all have the molecular formula C6H100, but oth products are constitutional isomers of one another. Stereochemistry should be shown if applicable. HO. Nah, DMSO Br HO, Nah, DMSO Br An efficient way to prepare asymmetrical ethers was developed by a British scientist, Alexander Williamson. Show what reagents you would use to prepare the following compound via a...
2. Fill in the missing reactants, reagents & conditions, or products. Don't worry about stereochemistry, unless...
2. Fill in the missing reactants, reagents & conditions, or products. Don't worry about stereochemistry, unless indicated. OH NaBH4, MeOH H' cat NaBH4, MeOH ме
1. fill in the boxes below with the reagents or major product(s): (2 pointe each, 12...
1. fill in the boxes below with the reagents or major
product(s): (2 pointe each, 12 points
1. Fill in the boxes below with the reagents or major organic product(s): (2 points each, 12 points) 1). KMn Oy . heat, H₂O 2). Hz0o soch Xs H N(CH2CH3 1) LiAIHA 2) H20 pyridine
2. Fill in the missing reactants, reagents & conditions, or products. Don't worry about stereochemistry, unless...
2. Fill in the missing reactants, reagents & conditions, or products. Don't worry about stereochemistry, unless indicated. 1. LDA, -78c OCH then H3o 0 CO Et H3o C10H100 CH NaOEt (aq) 0 0 NaOH (aq) NaOEt (aq) 0
answer all questions 5. Fill in the missing structures (products or reagents, including stereochemistry, if relevant)...
answer all questions
5. Fill in the missing structures (products or reagents, including stereochemistry, if relevant) and specify the most likely mechanism (SN1, S2, E1, E2) for formation of the product you have drawn. If a mixture will occur,show the major products. CH,ONa Сн,он нсулснэ H₃C Br HO H2O/acetone H₃C LIOH CH₂ H₂c a DMF 6. For the series shown below, label the most stable alkene, and the least stable alkene. CHE CH, CHE CH, -CH3
1. Determine whether the following reactions go through SN or SNP and write the products, with...
1. Determine whether the following reactions go through SN or SNP and write the products, with stereochemistry as applicable. BrNHz NaOEt Nal OMS KCN CI DMSO Br HO NaSH DMSO Tso CH3 Nal Acetone CH3 2. The following reactions each undergo SNmechanisms. For each explain why you would predict the substitution products to come from an SN2mechanism and fill in the product. If stereochemistry is given in the reactants, give the correct stereochemistry in the products. Cl + Z Na...
organic chemistry HELP ASAP! Fill in the boxes with the reagents, or major organic product(s) you...
organic chemistry HELP ASAP!
Fill in the boxes with the reagents, or major organic product(s) you would expect. Make sure to properly indicate the stereochemistry of the product(s) and indicate all stereoisomers formed 1) Mg. Et20 Br 2) PhCHO OH PCC 3) H30t 1) HB(Sia)2 2) NaOH H202 3) NaBH4 1) Mg. Et20 Br 2) PhCO2CH3 3) H30 DMSO (COCI)2 OH EtaN, CH2Cl2 1) Mg. Et2O 2) O 1) OsO4 H202 OH 3) H3o 2) PCC
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number...
Propose an efficient synthesis for the transformation below,
using two sequential reductive aminations. Enter
the appropriate number or letter from the reagent list handout.
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...
Please Pr 2. Fill in the missing reactants, reagents & conditions, or products. Show stereochemistry where...
Please Pr 2. Fill in the missing reactants, reagents & conditions, or products. Show stereochemistry where appropriate. 10 points. excess MgBr OH Me then H20 Ph3P OMe NH N﹀Me MeO MeO
Predicting Products: Draw the structure of the one major organic product of each reaction in the boxes provided. Be aware that the products all have the molecular formula C6H100, but oth products are constitutional isomers of one another. Stereochemistry should be shown if applicable. HO. Nah, DMSO Br HO, Nah, DMSO Br An efficient way to prepare asymmetrical ethers was developed by a British scientist, Alexander Williamson. Show what reagents you would use to prepare the following compound via a...
2. Fill in the missing reactants, reagents & conditions, or products. Don't worry about stereochemistry, unless indicated. OH NaBH4, MeOH H' cat NaBH4, MeOH ме
1. fill in the boxes below with the reagents or major
product(s): (2 pointe each, 12 points
1. Fill in the boxes below with the reagents or major organic product(s): (2 points each, 12 points) 1). KMn Oy . heat, H₂O 2). Hz0o soch Xs H N(CH2CH3 1) LiAIHA 2) H20 pyridine
2. Fill in the missing reactants, reagents & conditions, or products. Don't worry about stereochemistry, unless indicated. 1. LDA, -78c OCH then H3o 0 CO Et H3o C10H100 CH NaOEt (aq) 0 0 NaOH (aq) NaOEt (aq) 0
answer all questions
5. Fill in the missing structures (products or reagents, including stereochemistry, if relevant) and specify the most likely mechanism (SN1, S2, E1, E2) for formation of the product you have drawn. If a mixture will occur,show the major products. CH,ONa Сн,он нсулснэ H₃C Br HO H2O/acetone H₃C LIOH CH₂ H₂c a DMF 6. For the series shown below, label the most stable alkene, and the least stable alkene. CHE CH, CHE CH, -CH3
1. Determine whether the following reactions go through SN or SNP and write the products, with stereochemistry as applicable. BrNHz NaOEt Nal OMS KCN CI DMSO Br HO NaSH DMSO Tso CH3 Nal Acetone CH3 2. The following reactions each undergo SNmechanisms. For each explain why you would predict the substitution products to come from an SN2mechanism and fill in the product. If stereochemistry is given in the reactants, give the correct stereochemistry in the products. Cl + Z Na...
organic chemistry HELP ASAP!
Fill in the boxes with the reagents, or major organic product(s) you would expect. Make sure to properly indicate the stereochemistry of the product(s) and indicate all stereoisomers formed 1) Mg. Et20 Br 2) PhCHO OH PCC 3) H30t 1) HB(Sia)2 2) NaOH H202 3) NaBH4 1) Mg. Et20 Br 2) PhCO2CH3 3) H30 DMSO (COCI)2 OH EtaN, CH2Cl2 1) Mg. Et2O 2) O 1) OsO4 H202 OH 3) H3o 2) PCC
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...
Propose an efficient synthesis for the transformation below,
using two sequential reductive aminations. Enter
the appropriate number or letter from the reagent list handout.
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...
Please Pr 2. Fill in the missing reactants, reagents & conditions, or products. Show stereochemistry where appropriate. 10 points. excess MgBr OH Me then H20 Ph3P OMe NH N﹀Me MeO MeO
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