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10. Part A. (9 pt) Fill in any necessary reagents or intermediates in the empty boxes...
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
13. Reactions: Fill in the missing products for each of the boxes in the following reaction...
13. Reactions: Fill in the missing products for each of the boxes in the following reaction sequences. (30) OH Na2Cr2O7 H2SO4 H2O PCC NaBH HOCH, PBr3 Br2, H20 NaH BrMg- 2. H2O* NaOEt 1. OsO4 2. NaHSO3
Which sequence of reagents is necessary to carry out the following synthesis? (1) multiple steps OH Bry/hy; NaOH; R...
Which sequence of reagents is necessary to carry out the following synthesis? (1) multiple steps OH Bry/hy; NaOH; RCO;H; H30* Cl/heat; KOH; OsO4; NaHSO3/H2O H/Pd, NBS/H2O/DMSO: H:07 KOH; OsO4; NaHSO3/H20 NaOH; Brz/H20; KOH; H30+ o multiple steps o out "OH Page 2
Identify the reagents necessary to accomplish the following transformations: Choose from the following list of reagents:...
Identify the reagents necessary to accomplish the following transformations: Choose from the following list of reagents: 1) xẼ NaNH, 2) H20 10 g-BBN 2) H2O2, NaOH 1) ELMgBr 2) H2O 1) Hg(OAC)2, H20 2) NaBH4 1) TSCI, pyridine 2] -B40k 1) MeMgBr 2) H20 Brz 1) t-BuOK 2) TSCI, pyridine TSCI, pyridine Na2Cr2071) NaBH4 H2SO4, H20 20 H2O2, NaOH PCC, CH2Cl2 Enter the correct letter for each step of the reaction in the boxes below. (Reagents can be used more...
Using the reagents below, list in order (by letter, no period) those necessary to convert the...
Using the reagents below, list in order (by letter, no period) those necessary to convert the starting material into the given product: OE- Note: Not all spaces provided may be needed. Type "na" in any space where no reagent a. heat, -CO2 b. NaoEt c. (CH3CH2)2Culi d. CH2Cl2, PCC e. C3H COCH(C2H5)C(0)CH f. CH3CH2LI 9. HA, CHOH h. i. C2H5OC(O)(O)OC2H5, NaoEt il. H30* 1. HNC(O)NH2 3. H(CH3)2 k. OH, H20, heat then H30* 1. H30 Step . 1 Step Step...
3. Fill in the reagents or products for the following reactions. Note some boxes will require...
3. Fill in the reagents or products for the following reactions. Note some boxes will require two or three reagents in separate steps; list them as 1, 2, and 3. (2 points) 1. MeONa/MeOH 2. HCI +/ H2N Br 4. Using another sheet of paper, provide a reasonable reaction mechanism for the following transformation, starting with enamine generation (Carbonyls 2) and subsequent alkylation and hydrolysis (Carbonyls 3). Please write neatly and show all arrows, resonance structures, tetrahedral intermediates, and charges....
Fill in the boxes over each arrow with the letter that corresponds to the reagents needed to perform each step of the multistep synthesis show below. Reagents may be used more than once, or not at all...
Fill in the boxes over each arrow with the letter that
corresponds to the reagents needed to perform each step of the
multistep synthesis show below. Reagents may be used more than
once, or not at all. Pay close attention to the numbered carbons in
the starting material, and be sure that your answer accounts for
the position of these carbons in the final product.
pts) Fill in the boxes over each arrow with the letter that corresponds to the...
1) 2 (CH3),CHCH Br / Cul/ 4 Li? CHỊCH, CHỊCH 2) H30+ 2. Using any necessary reagents, show how the following synth...
1) 2 (CH3),CHCH Br / Cul/ 4 Li? CHỊCH, CHỊCH 2) H30+ 2. Using any necessary reagents, show how the following synthetic transformations may be achieved. Give reagents and conditions for each step. Include all synthetic intermediates compounds produced during the course of multi-step synthesis). NOTE: You may not use HOC OH 1. For each of the following questions, provide the missing reagents that can be purchased) and conditions or predict the MAJOR product. Indicate stereochemistry and identify a racemic...
organic chemistry 1.1 pt) Which reagent would you use to effect the following transformation of a...
organic chemistry
1.1 pt) Which reagent would you use to effect the following transformation of a diol into a keto acid? ОН Reagent? CH,CHCH,CH,CH,OH - CH,CCH,CH,сон a) Jones(H2Cr2O7) b) Tollens c) mCPBA d) Collins(PCC) e) LiAlH4 2.(2 pts) Circle the TWO compounds that yield a stable Grignard reagent when treated with magnesium in ether. Br CHÚC HỌC=CH- CH,OH HN 3.(2 pts each) Reactions. Complete each reaction shown here. HỌC=CH- + HC=CH- -CH OH он 1. CH CH MgBrCH,CH,CH=CHCCH2CH3 2.H2O Сн,...
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...
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
13. Reactions: Fill in the missing products for each of the boxes in the following reaction sequences. (30) OH Na2Cr2O7 H2SO4 H2O PCC NaBH HOCH, PBr3 Br2, H20 NaH BrMg- 2. H2O* NaOEt 1. OsO4 2. NaHSO3
Which sequence of reagents is necessary to carry out the following synthesis? (1) multiple steps OH Bry/hy; NaOH; RCO;H; H30* Cl/heat; KOH; OsO4; NaHSO3/H2O H/Pd, NBS/H2O/DMSO: H:07 KOH; OsO4; NaHSO3/H20 NaOH; Brz/H20; KOH; H30+ o multiple steps o out "OH Page 2
Identify the reagents necessary to accomplish the following transformations: Choose from the following list of reagents: 1) xẼ NaNH, 2) H20 10 g-BBN 2) H2O2, NaOH 1) ELMgBr 2) H2O 1) Hg(OAC)2, H20 2) NaBH4 1) TSCI, pyridine 2] -B40k 1) MeMgBr 2) H20 Brz 1) t-BuOK 2) TSCI, pyridine TSCI, pyridine Na2Cr2071) NaBH4 H2SO4, H20 20 H2O2, NaOH PCC, CH2Cl2 Enter the correct letter for each step of the reaction in the boxes below. (Reagents can be used more...
Using the reagents below, list in order (by letter, no period) those necessary to convert the starting material into the given product: OE- Note: Not all spaces provided may be needed. Type "na" in any space where no reagent a. heat, -CO2 b. NaoEt c. (CH3CH2)2Culi d. CH2Cl2, PCC e. C3H COCH(C2H5)C(0)CH f. CH3CH2LI 9. HA, CHOH h. i. C2H5OC(O)(O)OC2H5, NaoEt il. H30* 1. HNC(O)NH2 3. H(CH3)2 k. OH, H20, heat then H30* 1. H30 Step . 1 Step Step...
3. Fill in the reagents or products for the following reactions. Note some boxes will require two or three reagents in separate steps; list them as 1, 2, and 3. (2 points) 1. MeONa/MeOH 2. HCI +/ H2N Br 4. Using another sheet of paper, provide a reasonable reaction mechanism for the following transformation, starting with enamine generation (Carbonyls 2) and subsequent alkylation and hydrolysis (Carbonyls 3). Please write neatly and show all arrows, resonance structures, tetrahedral intermediates, and charges....
Fill in the boxes over each arrow with the letter that
corresponds to the reagents needed to perform each step of the
multistep synthesis show below. Reagents may be used more than
once, or not at all. Pay close attention to the numbered carbons in
the starting material, and be sure that your answer accounts for
the position of these carbons in the final product.
pts) Fill in the boxes over each arrow with the letter that corresponds to the...
1) 2 (CH3),CHCH Br / Cul/ 4 Li? CHỊCH, CHỊCH 2) H30+ 2. Using any necessary reagents, show how the following synthetic transformations may be achieved. Give reagents and conditions for each step. Include all synthetic intermediates compounds produced during the course of multi-step synthesis). NOTE: You may not use HOC OH 1. For each of the following questions, provide the missing reagents that can be purchased) and conditions or predict the MAJOR product. Indicate stereochemistry and identify a racemic...
organic chemistry
1.1 pt) Which reagent would you use to effect the following transformation of a diol into a keto acid? ОН Reagent? CH,CHCH,CH,CH,OH - CH,CCH,CH,сон a) Jones(H2Cr2O7) b) Tollens c) mCPBA d) Collins(PCC) e) LiAlH4 2.(2 pts) Circle the TWO compounds that yield a stable Grignard reagent when treated with magnesium in ether. Br CHÚC HỌC=CH- CH,OH HN 3.(2 pts each) Reactions. Complete each reaction shown here. HỌC=CH- + HC=CH- -CH OH он 1. CH CH MgBrCH,CH,CH=CHCCH2CH3 2.H2O Сн,...
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...
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QUESTION 8
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