Homework Answers
based on the reactivity of reagent and the conditions the products formed as follows
Add Answer to:
Starting Material Conditions OH PBr3 Eto C NaCN OMs DMF Br NaNH DMSO, 20°C 8 hr...
Conditions Starting Material Major Product(s) OH PBrg Et20 NaCN DMF OMs NaNH2 DMSO, 20'C 8 hr...
Conditions Starting Material Major Product(s) OH PBrg Et20 NaCN DMF OMs NaNH2 DMSO, 20'C 8 hr 1) NaH, DMF, -78°C 2) A ci NaOH Br OH
ETOH -Br heat - Br k. NaOH DMSO NaCN Br DMF m. OH Jones reagent
ETOH -Br heat - Br k. NaOH DMSO NaCN Br DMF m. OH Jones reagent
• Please provide the major organic product(s) of the reaction as described Account for all stereochemistry requirem...
• Please provide the major organic product(s) of the reaction as described Account for all stereochemistry requirements for reaction and products. You need not include byproducts such as salts for this assignment, but you should be aware of their presence. "No reaction is NOT a possibility on this assignment Starting Material Conditions Major Product(s) ОН PBr3 Et20 NaCN DMF NaNH2 DMSO, 20'C 8 hr 1) NaH, DMF, -78°C 2) M ai NaOH
• Please provide the major organic product(s) of the reaction as described. Account for all stereochemistry...
• Please provide the major organic product(s) of the reaction as described. Account for all stereochemistry requirements for reaction and products. You need not include byproducts such as salts for this assignment, but you should be aware of their presence. "No reaction" is NOT a possibility on this assignment. Starting Material Conditions Major Product(s) ОН PB13 Et20 NaCN OMs DMF Br NaNH2 DMSO, 20'C 8 hr
Hi I need help predicting the products for these reactions OEt NaOCH.CH CH,CH OH b. H,...
Hi I need help predicting the products for these
reactions
OEt NaOCH.CH CH,CH OH b. H, O/H,0 a. NaOCH.CH CH,CH,OH b. Br c. NaOHH O, beat d. H2O*/H2O 1. NaCN, DMSO 2. CH,MgBr, Eto 3. H.O/H,O EN 2. NaH, CH,Br chemoselective 1. a. NaOet, EtOH Br b. 2. a. NaOH/H,O, heat b. H30+/H20 CY.NECEN cy OH b. then add HC-NH2 a. NaCN, DMSO b. HO*/H,0
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and...
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
Devise the most efficient synthesis for the carboxylic acid below using a starting material and reagents...
Devise the most efficient synthesis for the carboxylic acid
below using a starting material and reagents from the tables. Give
your route by specifying the number of the starting material
followed by the letters of the reagents you would use beginning
with the first step.
The answer 4fh means treat t-butanol(4)
with conc. HCl(f) then treat the product with KOH in
alcohol(h).
please write legible and circle answer
OH rting materials Br Br ve tor OH нс 3 OH Он...
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2)...
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2) CH3CH2Br Он, H2O 1) NaOEt 8 2) NaOEt OEt 10 Cl NaH 2 (excess) 12 HO Bra(excess) 13 HO LDA 14L THF, -78 C NaOEt, EtOH NaOEt, EtOH 16 NaOEt, EtOH 17 Br но 18 OOEt 1)NaOEt, EtOH 2) H3O 19 OEt 20 l HO o CHO + H20
Please show detailed mechanism or explain in words. DQ25.11 Homework Draw the starting material: . SOCI,...
Please show detailed mechanism or explain in words.
DQ25.11 Homework Draw the starting material: . SOCI, DMF 2. (CH,CH),CuLi, THF Ph 3. H,O Hint: Note that organocuprates only add once to acyl chlorides. DQ25.12 Homework Draw the product of the following reactions: 0 O HN CH CI NaBH (1 equiv.) EtOH Hint: Think about the reactivity of the carboxylic acid derivatives. DQ25.13 Homework Draw the product of the following reaction. CH,NO cc, tBuOK, DMSO CCI Hint: The first step in...
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List...
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
Conditions Starting Material Major Product(s) OH PBrg Et20 NaCN DMF OMs NaNH2 DMSO, 20'C 8 hr 1) NaH, DMF, -78°C 2) A ci NaOH Br OH
ETOH -Br heat - Br k. NaOH DMSO NaCN Br DMF m. OH Jones reagent
• Please provide the major organic product(s) of the reaction as described Account for all stereochemistry requirements for reaction and products. You need not include byproducts such as salts for this assignment, but you should be aware of their presence. "No reaction is NOT a possibility on this assignment Starting Material Conditions Major Product(s) ОН PBr3 Et20 NaCN DMF NaNH2 DMSO, 20'C 8 hr 1) NaH, DMF, -78°C 2) M ai NaOH
• Please provide the major organic product(s) of the reaction as described. Account for all stereochemistry requirements for reaction and products. You need not include byproducts such as salts for this assignment, but you should be aware of their presence. "No reaction" is NOT a possibility on this assignment. Starting Material Conditions Major Product(s) ОН PB13 Et20 NaCN OMs DMF Br NaNH2 DMSO, 20'C 8 hr
Hi I need help predicting the products for these
reactions
OEt NaOCH.CH CH,CH OH b. H, O/H,0 a. NaOCH.CH CH,CH,OH b. Br c. NaOHH O, beat d. H2O*/H2O 1. NaCN, DMSO 2. CH,MgBr, Eto 3. H.O/H,O EN 2. NaH, CH,Br chemoselective 1. a. NaOet, EtOH Br b. 2. a. NaOH/H,O, heat b. H30+/H20 CY.NECEN cy OH b. then add HC-NH2 a. NaCN, DMSO b. HO*/H,0
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
Devise the most efficient synthesis for the carboxylic acid
below using a starting material and reagents from the tables. Give
your route by specifying the number of the starting material
followed by the letters of the reagents you would use beginning
with the first step.
The answer 4fh means treat t-butanol(4)
with conc. HCl(f) then treat the product with KOH in
alcohol(h).
please write legible and circle answer
OH rting materials Br Br ve tor OH нс 3 OH Он...
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2) CH3CH2Br Он, H2O 1) NaOEt 8 2) NaOEt OEt 10 Cl NaH 2 (excess) 12 HO Bra(excess) 13 HO LDA 14L THF, -78 C NaOEt, EtOH NaOEt, EtOH 16 NaOEt, EtOH 17 Br но 18 OOEt 1)NaOEt, EtOH 2) H3O 19 OEt 20 l HO o CHO + H20
Please show detailed mechanism or explain in words.
DQ25.11 Homework Draw the starting material: . SOCI, DMF 2. (CH,CH),CuLi, THF Ph 3. H,O Hint: Note that organocuprates only add once to acyl chlorides. DQ25.12 Homework Draw the product of the following reactions: 0 O HN CH CI NaBH (1 equiv.) EtOH Hint: Think about the reactivity of the carboxylic acid derivatives. DQ25.13 Homework Draw the product of the following reaction. CH,NO cc, tBuOK, DMSO CCI Hint: The first step in...
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
Most questions answered within 3 hours.
-
1-Write an algorithm to get two numbers from the user (as
inputs) and calculate the sum...
asked 14 seconds from now -
Define white-collar crime. What is the difference between
offender and offense-based definitions of white-collar crime? What...
asked 41 minutes ago -
Consider a reaction which is 1st order with respect to A and 1st
order with respect...
asked 51 minutes ago -
c++
The length of the hypotenuse of a right-angled triangle is the
square root of the...
asked 58 minutes ago -
When a metal rod is heated, not only its resistance but also its
length and cross‐sectional...
asked 1 hour ago -
write a c++ program that computes the L^1 - Norm of a given
vector (L^1 norm...
asked 1 hour ago -
A manufacturer of banana chips would like to know whether its
bag filling machine works correctly...
asked 1 hour ago -
Complete the chapter case, "Turnover Analysis".
Chapter Case
Turnover Analysis
You recently completed your company’s new...
asked 1 hour ago -
What is the pH of solutions having the following H3O+
concentrations? Identify each as acidic, basic,...
asked 1 hour ago -
How does over-voltage of the diode usually occur?
asked 1 hour ago -
If you step on a dirty nail, your doctor will recommend you
update your Tetanus vaccination....
asked 1 hour ago -
Suppose that decreases in the price of milk lead to decrease s
in the retail prices...
asked 1 hour ago