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22. Predict the products or the reagents. (5 pts...... 1 pt. each) H3C о 1. (CH3)2NH...
This is for my organic chemistry homework. I don’t require an explanation for this, just the...
This is for my organic chemistry homework. I don’t require an
explanation for this, just the answer. I’m just trying to survive
this class. I also have a term paper that I’m writing tonight.
Whatever you can help me with is great, but please answer as much
and as quickly as you can. It’s due tonight. Thanks.
Write the answers for the following ON the Answer Sheet's given space 22. Predict the products or the reagents. (5 pts..... pt. each)...
1. Predict the products of the following reactions. CH3 TsCl Pyridine NaCN CH3 PBr3 Pyridine NaCN...
1. Predict the products of the following reactions. CH3 TsCl Pyridine NaCN CH3 PBr3 Pyridine NaCN (1) BH3:THF (2) H2O2,OH H2SO4(cat.) H2O (1) Hg(OAc)2 (2) NaBH/OH 2. Write the mechanism of the following reactions он но он Ph BF3 Ph
14. (1 pt each) Name the following molecules. CH3 CH3 нно н н-с-с-с-NA ті Hн н,с...
14. (1 pt each) Name the following molecules. CH3 CH3 нно н н-с-с-с-NA ті Hн н,с Сн, Н CH,CH нс H 15. (3 pts each) Give the product(s) for the following reactions, and name all reactants and products. CH, он ОН н,с + нэс- сн - сн 3 нус. NH2 ОН Hн ІІ ОН + н-с-с-о-н НО P н Н ОН
10). (18 pts) Predict the structures of the products from each of the following S2 reactions....
10). (18 pts) Predict the structures of the products from each of the following S2 reactions. If no reaction is expected, write "No Rxn" Hас. H,с-о° Br A). н,с- он сH H,с. KBr сH, В). acetone он NaN С). ethanol Br CH3 кCN D). H,с. Br DMSO сн, SH но E) CH3 ethanol "сH,
(24 pts) 3. Predict the product(s) for each reaction. Indicate stereochemistry if known. If more than...
(24 pts) 3. Predict the product(s) for each reaction. Indicate stereochemistry if known. If more than one product is predicted, circle the one you think would be major. If there is no reaction expected, then indicate NR. а. HaCl.. Br NaCN THF b. Н—Br ether ОН с. CH3 КОН Br THF d. НОСН heat е. PBr3 ОН ether f. ОН NaSCH3 Hо g. cat Br H2SO4 heat ОН h Br H но heat Br
Propose the missing products /reagents 1. (35 pts) Propose any 10 out of 18 missing reagents/products...
Propose the missing products /reagents
1. (35 pts) Propose any 10 out of 18 missing reagents/products (if any). Mark them with an aster (only 10 will be graded). (3 pts for ench correct answer, 1 pts for each incorrect answer, final pt adjusted to 35 pts maximum): Ph 2 steps H,Cro Phot он 1) ( 17. PhCI Phoн HgSO4 но 15 16. PhH2) PCC Phcн,
22) What is the product of the following reaction? (t о H2, Pt A) 1,2-cyclohexanediol C)...
22) What is the product of the following reaction? (t о H2, Pt A) 1,2-cyclohexanediol C) cyclohexene B) cyclohexanol D) cyclohexane 23) What is the product of the following reaction? (2 H3C CH3 OsO4, (CH3)3COOH C=C (CH)3СОН, ОН н н B) cis-2,3-epoxybutane A) CH3CH-O C) 2,3-butanediol D) 1,3-butanediol 24) 24) Which of the following reagents will convert cyclohexene into cis-1,2-cyclohexanediol? HO CHP HOll. yn A) CH3CO3H (peroxyacetic acid) B) OsO4, (CH3)3 COOH, (CH3)3COH, OH C) 03 followed by Zn/H20 D)...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2-chloro-2-methylpropane reacts with water in three steps to yield 2-methylpropan-2-ol. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. estion 6 1pt Arrow-pushing Instructions Question 7 1 pt Question 8 Question Question 10 1 pt pt pe...
Chapter 6 [References) Question 15 1 pt CI CI Question 16 1 pt HCI H3C CH3...
Chapter 6 [References) Question 15 1 pt CI CI Question 16 1 pt HCI H3C CH3 HC Question 17 CH3 H3C CH3 1 pt Question 18 1 pt H2C CH3 CI Question 19 1 pt CH3 H2C CH3 CI Question 20 1 pt Question 21 ® 1 pt Treating 1,3-pentadiene with one mole of HCl give a mixture of five isomeric products. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism Question 22...
8. Predict the major organic products of each of the following reaction conditions (20 points) 1)...
8. Predict the major organic products of each of the following reaction conditions (20 points) 1) LiAIH diethylether н 4 2) Н-о Н.о KOH CrO,, H,SO,, H,О он acetone (co-solvent) 1) CH3MgBr, diethylether 2) Н-о 9. Show how you could synthesize the targeted products from the starting epoxides. Show all reagents and reaction conditions in the boxes above the reaction arrows Но Hас ОСHЗ но O
This is for my organic chemistry homework. I don’t require an
explanation for this, just the answer. I’m just trying to survive
this class. I also have a term paper that I’m writing tonight.
Whatever you can help me with is great, but please answer as much
and as quickly as you can. It’s due tonight. Thanks.
Write the answers for the following ON the Answer Sheet's given space 22. Predict the products or the reagents. (5 pts..... pt. each)...
1. Predict the products of the following reactions. CH3 TsCl Pyridine NaCN CH3 PBr3 Pyridine NaCN (1) BH3:THF (2) H2O2,OH H2SO4(cat.) H2O (1) Hg(OAc)2 (2) NaBH/OH 2. Write the mechanism of the following reactions он но он Ph BF3 Ph
14. (1 pt each) Name the following molecules. CH3 CH3 нно н н-с-с-с-NA ті Hн н,с Сн, Н CH,CH нс H 15. (3 pts each) Give the product(s) for the following reactions, and name all reactants and products. CH, он ОН н,с + нэс- сн - сн 3 нус. NH2 ОН Hн ІІ ОН + н-с-с-о-н НО P н Н ОН
10). (18 pts) Predict the structures of the products from each of the following S2 reactions. If no reaction is expected, write "No Rxn" Hас. H,с-о° Br A). н,с- он сH H,с. KBr сH, В). acetone он NaN С). ethanol Br CH3 кCN D). H,с. Br DMSO сн, SH но E) CH3 ethanol "сH,
(24 pts) 3. Predict the product(s) for each reaction. Indicate stereochemistry if known. If more than one product is predicted, circle the one you think would be major. If there is no reaction expected, then indicate NR. а. HaCl.. Br NaCN THF b. Н—Br ether ОН с. CH3 КОН Br THF d. НОСН heat е. PBr3 ОН ether f. ОН NaSCH3 Hо g. cat Br H2SO4 heat ОН h Br H но heat Br
Propose the missing products /reagents
1. (35 pts) Propose any 10 out of 18 missing reagents/products (if any). Mark them with an aster (only 10 will be graded). (3 pts for ench correct answer, 1 pts for each incorrect answer, final pt adjusted to 35 pts maximum): Ph 2 steps H,Cro Phot он 1) ( 17. PhCI Phoн HgSO4 но 15 16. PhH2) PCC Phcн,
22) What is the product of the following reaction? (t о H2, Pt A) 1,2-cyclohexanediol C) cyclohexene B) cyclohexanol D) cyclohexane 23) What is the product of the following reaction? (2 H3C CH3 OsO4, (CH3)3COOH C=C (CH)3СОН, ОН н н B) cis-2,3-epoxybutane A) CH3CH-O C) 2,3-butanediol D) 1,3-butanediol 24) 24) Which of the following reagents will convert cyclohexene into cis-1,2-cyclohexanediol? HO CHP HOll. yn A) CH3CO3H (peroxyacetic acid) B) OsO4, (CH3)3 COOH, (CH3)3COH, OH C) 03 followed by Zn/H20 D)...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2-chloro-2-methylpropane reacts with water in three steps to yield 2-methylpropan-2-ol. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. estion 6 1pt Arrow-pushing Instructions Question 7 1 pt Question 8 Question Question 10 1 pt pt pe...
Chapter 6 [References) Question 15 1 pt CI CI Question 16 1 pt HCI H3C CH3 HC Question 17 CH3 H3C CH3 1 pt Question 18 1 pt H2C CH3 CI Question 19 1 pt CH3 H2C CH3 CI Question 20 1 pt Question 21 ® 1 pt Treating 1,3-pentadiene with one mole of HCl give a mixture of five isomeric products. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism Question 22...
8. Predict the major organic products of each of the following reaction conditions (20 points) 1) LiAIH diethylether н 4 2) Н-о Н.о KOH CrO,, H,SO,, H,О он acetone (co-solvent) 1) CH3MgBr, diethylether 2) Н-о 9. Show how you could synthesize the targeted products from the starting epoxides. Show all reagents and reaction conditions in the boxes above the reaction arrows Но Hас ОСHЗ но O
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