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the missing starting materials, reagents, or...
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+...
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+ OH CH,OH NaOH Meo NH2 room temp. HO OH Meo Me ОН Meo 2. Provide appropriate conditions to convert each of the following starting mana hexanoic acid (some transformations may require more than one step): It each of the following starting materials into OH OH ОMe "NH₂
Q2. Provide the missing information of the following reactions. (such as reagents, starting materials, products_etc.) 21...
Q2. Provide the missing information of the following reactions. (such as reagents, starting materials, products_etc.) 21 1. CH,CH-CH=PP 1-Propanol 2-methylpentan-3-one H+, heat H2N Н. + HO- Н HO- + Y. H trace HCI H НО. OH H3C сн. H30.4 H2CH2CO OCH CH3
Part II. Complete the Reactions. Complete the reactions by filling in the missing starting materials, reagents,...
Part II. Complete the Reactions. Complete the
reactions by filling in the missing starting materials,
reagents, or products (4 pts each; 24 pts total).
Part lIl. Complete the Reactions. Complete the reactions by filling in the missing starting materials, reagents, or products (4 pts each; 24 pts total). 1. NaOEt <排鞏 2. 2. PhBr 1. LiAIH4 CD H+. Gl2 Br
-if you would please check my answers on the bottom section -fill in the top section...
-if
you would please check my answers on the bottom section
-fill in the top section
provide the appropriate starting material, reagents or products for the following reactions 0 1. LDA cold 2. ethylbromide NH 0 он OH 1. LIG ) 2. Holgerich CH, OH H,50 1. CH, ME 2. H o quenchi DIBAL 1. NaBHY Na, Cro, H2SO4 2. HO (quench)
II. Reactions: Predict the major organic product(s) or write the appropriate reagents/starting materials for the following...
II. Reactions: Predict the major organic product(s) or write the appropriate reagents/starting materials for the following reactions. Indicate stereochemistry and regiochemistry when appropriate. Indicate reactions that are expected to result in a racemic mixture of products DBr 1. Н.О, CHCI он HSO, heat кон 1) вн, THF 3. 2) H202. HO 1) Hg(OAc)2, CH,OH 2) NaBH, OH 5. Br2 SH 6. HIO4 OH THF, H2O "он III. Synthesis: Starting from the alkenyl bromide below, devise a synthesis that produces the...
Devise a synthesis of (Z)-3-octene using one of the starting materials and any of the reagents...
Devise a synthesis of (Z)-3-octene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps Starting materials нсисынсно-си нос-сцен нос-cң соң,он нонс Reagents + NaNH / NH diodo ethane 1-bromo-3-methybutane H undar catalyst + NaOH HẠO e 1-bromopropane butyl bromide күн clodomethane 1 2-bromopropane H/Pd on carbon I N/NH0 Starting material Reagent for step 1...
7. Predict the major organic product or provide reagents needed to complete each reaction. 1. CH3NH2...
7. Predict the major organic product or provide reagents needed to complete each reaction. 1. CH3NH2 (a-b) excess 2. LIAIHA 3. H20 ia -NH ?? excess (c-d) HO NH2 triethylamine ? (e-f) CEN 1. CHẠMgBr 2. H20, H NH2 (g-h) H20, H* H2. Pd (1-1) CH3NH2 4 products (m) 1. LAIH 2. H2O, H & NH (n) 1. LiAIH4 2. H20, H+ 8. Predict the four possible Aldol condensation products and their dehydration products. KOH, H20.A + H 1. Predict...
(10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products....
(10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products. Then for each reaction draw the reaction mechanism with correct electron flow arrows if appropriate or intermediates and correct formal charges. -OH -NH2 NH (10 points) Use the Gabrielle synthesis to make your starting amine below. Then use this starting amine to synthesize the secondary amine using reductive amination. Draw the mechanisms for both reactions below. Be sure to draw correct intermediates, electron flow...
Devise a synthesis of (Z)-4-methyl-2-pentene using one of the starting materials and any of the reagents...
Devise a synthesis of (Z)-4-methyl-2-pentene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials HC=CH HC=C-CH, HC=C-CH,CH, сн. HC=C-CH2CH2CH2CH2HC=C-C-CH, von CH, HC=C-¢-CH, . CHO Reagents a NaNH, NH(l) diodoethane g 1-bromo-3-methylbutane į Hy / Lindlar catalyst - Na0H: H0 e 1-bromopropane ht-butyl bromide k H / NH (1) ciodomethane f 2-bromopropane i...
1. Provide products for the following reactions. Show appropriate stereochemistry where appropriate. HI H2SO4 CH,OH 1....
1. Provide products for the following reactions. Show appropriate stereochemistry where appropriate. HI H2SO4 CH,OH 1. Hg(OAc),/H,0 2. NaBH4 1. BH; 2. H,Oz/NaOH H/Pd H2SO4/H2O 4. Provide the missing reagents or starting materials in the following reactions. OH Br HO 1. Br2 2, NaNH (excess) 3. H2O
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+ OH CH,OH NaOH Meo NH2 room temp. HO OH Meo Me ОН Meo 2. Provide appropriate conditions to convert each of the following starting mana hexanoic acid (some transformations may require more than one step): It each of the following starting materials into OH OH ОMe "NH₂
Q2. Provide the missing information of the following reactions. (such as reagents, starting materials, products_etc.) 21 1. CH,CH-CH=PP 1-Propanol 2-methylpentan-3-one H+, heat H2N Н. + HO- Н HO- + Y. H trace HCI H НО. OH H3C сн. H30.4 H2CH2CO OCH CH3
Part II. Complete the Reactions. Complete the
reactions by filling in the missing starting materials,
reagents, or products (4 pts each; 24 pts total).
Part lIl. Complete the Reactions. Complete the reactions by filling in the missing starting materials, reagents, or products (4 pts each; 24 pts total). 1. NaOEt <排鞏 2. 2. PhBr 1. LiAIH4 CD H+. Gl2 Br
-if
you would please check my answers on the bottom section
-fill in the top section
provide the appropriate starting material, reagents or products for the following reactions 0 1. LDA cold 2. ethylbromide NH 0 он OH 1. LIG ) 2. Holgerich CH, OH H,50 1. CH, ME 2. H o quenchi DIBAL 1. NaBHY Na, Cro, H2SO4 2. HO (quench)
II. Reactions: Predict the major organic product(s) or write the appropriate reagents/starting materials for the following reactions. Indicate stereochemistry and regiochemistry when appropriate. Indicate reactions that are expected to result in a racemic mixture of products DBr 1. Н.О, CHCI он HSO, heat кон 1) вн, THF 3. 2) H202. HO 1) Hg(OAc)2, CH,OH 2) NaBH, OH 5. Br2 SH 6. HIO4 OH THF, H2O "он III. Synthesis: Starting from the alkenyl bromide below, devise a synthesis that produces the...
Devise a synthesis of (Z)-3-octene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps Starting materials нсисынсно-си нос-сцен нос-cң соң,он нонс Reagents + NaNH / NH diodo ethane 1-bromo-3-methybutane H undar catalyst + NaOH HẠO e 1-bromopropane butyl bromide күн clodomethane 1 2-bromopropane H/Pd on carbon I N/NH0 Starting material Reagent for step 1...
7. Predict the major organic product or provide reagents needed to complete each reaction. 1. CH3NH2 (a-b) excess 2. LIAIHA 3. H20 ia -NH ?? excess (c-d) HO NH2 triethylamine ? (e-f) CEN 1. CHẠMgBr 2. H20, H NH2 (g-h) H20, H* H2. Pd (1-1) CH3NH2 4 products (m) 1. LAIH 2. H2O, H & NH (n) 1. LiAIH4 2. H20, H+ 8. Predict the four possible Aldol condensation products and their dehydration products. KOH, H20.A + H 1. Predict...
(10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products. Then for each reaction draw the reaction mechanism with correct electron flow arrows if appropriate or intermediates and correct formal charges. -OH -NH2 NH (10 points) Use the Gabrielle synthesis to make your starting amine below. Then use this starting amine to synthesize the secondary amine using reductive amination. Draw the mechanisms for both reactions below. Be sure to draw correct intermediates, electron flow...
Devise a synthesis of (Z)-4-methyl-2-pentene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials HC=CH HC=C-CH, HC=C-CH,CH, сн. HC=C-CH2CH2CH2CH2HC=C-C-CH, von CH, HC=C-¢-CH, . CHO Reagents a NaNH, NH(l) diodoethane g 1-bromo-3-methylbutane į Hy / Lindlar catalyst - Na0H: H0 e 1-bromopropane ht-butyl bromide k H / NH (1) ciodomethane f 2-bromopropane i...
1. Provide products for the following reactions. Show appropriate stereochemistry where appropriate. HI H2SO4 CH,OH 1. Hg(OAc),/H,0 2. NaBH4 1. BH; 2. H,Oz/NaOH H/Pd H2SO4/H2O 4. Provide the missing reagents or starting materials in the following reactions. OH Br HO 1. Br2 2, NaNH (excess) 3. H2O
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