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This is for Organic II. Thank you!
1) For each of the reactions given below, provide...
This is for Organic II. Thank you! for each of the reactions given below, provide the...
This is for Organic II. Thank you!
for each of the reactions given below, provide the reagent
that should produce the transformation indicated. In each case,
more than one reagent is required for the transformation.
N(CH3)2 он b) ос-Hs он он он но Br
3) (4 points each) For each of the reactions given below, provide the reagent that should...
3) (4 points each) For each of the reactions given below, provide the reagent that should produce the transformation indicated. In each case, more than one reagent is required for the transformation. ОН N(CH3)2 LOC₂H5 ОН HO
1. Provide the missing starting material, reagents, or major organic product for each of the following...
1. Provide the missing starting material, reagents, or major organic product for each of the following reactions. (No more than two steps are required in any case where we ask you to fill in reagents.) 1. Mgo, Et20 2. H20 a) Cl b) MgBr OH , Et20 2. H* workup c) OH d) NaOH (cat.) e) OH NaBH4, CeCl3, MeOH
This is for Organic II. Thank you! 5) Consider Compounds I & II shown below. The...
This is for Organic II. Thank you!
5) Consider Compounds I & II shown below. The two compounds can undergo reactions 1 and 2 to yield Compound Q. a) (4 points) Draw the structure for Compound Q. b) (8 points - 4 points each) Give the reagents 1 and 2 that will produce Q, and explain how the reactions are similar or different. Q-•la
8. [18 pts) Provide the expected organic product(s) from each of the reactions below. Ignore the...
8. [18 pts) Provide the expected organic product(s) from each of the reactions below. Ignore the stereochemistry. No mechanism required! (3 points for each organic product, switching the major and minor will be penalized) a. Major: NaOCH; E2 Br b. Major Minor OH E2 Br 3 products in total CH,OH ΕΙ 6. 19 pts] For each of the following reactions, give the organic product(s), and include the stereochemistry when applicable. No mechanism required! (3 points for each organic product) a....
This is for Organic II. Thank you! Give the primary product that would result from the...
This is for Organic II. Thank you!
Give the primary product that would result from the following reactions: NOTE: If the problem involves multiple reactions, and you cannot determine the final product, draw the structure of any of the intermediate products (and indicate which reaction the product is for, i.e. Step # 1 , Step # 2 , etc.) 1) BHs, THF 2) н.о,. он-) 3) (CH3)2NH 4) H2, Pt/C Cat. н. он N-CH3 b) 1) н,о'*) 2) Na2Cr o,,...
3. Provide a full arrow-pushing mechanism for each of the following reactions. Wood CHAMBRE Cascos - LX i. CH3MgBr...
3. Provide a full arrow-pushing mechanism for each of the following reactions. Wood CHAMBRE Cascos - LX i. CH3MgBr (excess) ii. H+ OH OCH; 4. Provide the major product of the following reaction and provide a mechanism for its formation. HO1 OH A 5. You need to synthesize a large amount of molecule C, and you have just enough of each of molecules A and B in your chemical inventory. Provide a synthetic route showing how you can efficiently synthesize...
please answer all question and provide explanation or mechanism for each. thank you. 19. What is...
please answer all question and provide explanation or mechanism for
each. thank you.
19. What is the best choice of reagent(s) to perform the following transformation? OCHA a. CH,OH, H,SO b. CH:I, H2SO4 c. NaOCH d. CH,Li 20. What is the major organic product obtained from the following reaction of ethyl benzoate with the OH нс ск 1. 2 eq. CH3MOCI | Phocн,сн, 2. H,0* PhDcн, CH Ph CH P OHP OCH CHE a. b. 1 2 3 4 C....
CONCEPT QUESTION Predict the Product. Provide the stable organic product(s) for the reactions below. MgBr (1...
CONCEPT QUESTION Predict the Product. Provide the stable organic product(s) for the reactions below. MgBr (1 eq.) anto como HO 1. Mgº, CH3CH2OCH2CH3 3. H20, HCI Mechanism. Though alkoxides are not often considered as "good" leaving groups in the first semester of organic chemistry, under the "basic" conditions of a Grignard reagent, they are able to leave similarly to the halogen in acid halides. Using ChemDraw, provide the complete mechanism for the following transformation. You must include appropriate arrows, intermediates,...
please help me with the reactions listed II. Reactions. Fill in the correct product(s) from the...
please help me with the reactions listed
II. Reactions. Fill in the correct product(s) from the given starting material and reaction conditions, or give the proper reagent to transform the given starting material into the given product 1. CH₂ CH-OH + CH3--OH CH la Write the name of each reactant and product under the structures in the reaction above (1 point cach). 2. CH, CHẠho-6-OH + NaOH CHE 1 CH-CHS Сн che - CHLOHoté __.CH — answer below CH3-CH-CH2OH *...
This is for Organic II. Thank you!
for each of the reactions given below, provide the reagent
that should produce the transformation indicated. In each case,
more than one reagent is required for the transformation.
N(CH3)2 он b) ос-Hs он он он но Br
3) (4 points each) For each of the reactions given below, provide the reagent that should produce the transformation indicated. In each case, more than one reagent is required for the transformation. ОН N(CH3)2 LOC₂H5 ОН HO
1. Provide the missing starting material, reagents, or major organic product for each of the following reactions. (No more than two steps are required in any case where we ask you to fill in reagents.) 1. Mgo, Et20 2. H20 a) Cl b) MgBr OH , Et20 2. H* workup c) OH d) NaOH (cat.) e) OH NaBH4, CeCl3, MeOH
This is for Organic II. Thank you!
5) Consider Compounds I & II shown below. The two compounds can undergo reactions 1 and 2 to yield Compound Q. a) (4 points) Draw the structure for Compound Q. b) (8 points - 4 points each) Give the reagents 1 and 2 that will produce Q, and explain how the reactions are similar or different. Q-•la
8. [18 pts) Provide the expected organic product(s) from each of the reactions below. Ignore the stereochemistry. No mechanism required! (3 points for each organic product, switching the major and minor will be penalized) a. Major: NaOCH; E2 Br b. Major Minor OH E2 Br 3 products in total CH,OH ΕΙ 6. 19 pts] For each of the following reactions, give the organic product(s), and include the stereochemistry when applicable. No mechanism required! (3 points for each organic product) a....
This is for Organic II. Thank you!
Give the primary product that would result from the following reactions: NOTE: If the problem involves multiple reactions, and you cannot determine the final product, draw the structure of any of the intermediate products (and indicate which reaction the product is for, i.e. Step # 1 , Step # 2 , etc.) 1) BHs, THF 2) н.о,. он-) 3) (CH3)2NH 4) H2, Pt/C Cat. н. он N-CH3 b) 1) н,о'*) 2) Na2Cr o,,...
3. Provide a full arrow-pushing mechanism for each of the following reactions. Wood CHAMBRE Cascos - LX i. CH3MgBr (excess) ii. H+ OH OCH; 4. Provide the major product of the following reaction and provide a mechanism for its formation. HO1 OH A 5. You need to synthesize a large amount of molecule C, and you have just enough of each of molecules A and B in your chemical inventory. Provide a synthetic route showing how you can efficiently synthesize...
please answer all question and provide explanation or mechanism for
each. thank you.
19. What is the best choice of reagent(s) to perform the following transformation? OCHA a. CH,OH, H,SO b. CH:I, H2SO4 c. NaOCH d. CH,Li 20. What is the major organic product obtained from the following reaction of ethyl benzoate with the OH нс ск 1. 2 eq. CH3MOCI | Phocн,сн, 2. H,0* PhDcн, CH Ph CH P OHP OCH CHE a. b. 1 2 3 4 C....
CONCEPT QUESTION Predict the Product. Provide the stable organic product(s) for the reactions below. MgBr (1 eq.) anto como HO 1. Mgº, CH3CH2OCH2CH3 3. H20, HCI Mechanism. Though alkoxides are not often considered as "good" leaving groups in the first semester of organic chemistry, under the "basic" conditions of a Grignard reagent, they are able to leave similarly to the halogen in acid halides. Using ChemDraw, provide the complete mechanism for the following transformation. You must include appropriate arrows, intermediates,...
please help me with the reactions listed
II. Reactions. Fill in the correct product(s) from the given starting material and reaction conditions, or give the proper reagent to transform the given starting material into the given product 1. CH₂ CH-OH + CH3--OH CH la Write the name of each reactant and product under the structures in the reaction above (1 point cach). 2. CH, CHẠho-6-OH + NaOH CHE 1 CH-CHS Сн che - CHLOHoté __.CH — answer below CH3-CH-CH2OH *...
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