Homework Answers
First Friedal-Crafts alkylation then with Kmno4 which is a strong oxidizing agent and oxidize the benzyl carbon to COOH.
Then Chlorination at meta to COOH group.
Since COOH is meta directing group.
First and last steps are examples for aromatic Electrophilic substitution.
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Two Step Reaction -> CooH 1. What reagent(s) would you use...
Please show every step and write clearly. I want to learn how to perform this mechanism....
Please show every step and write clearly. I want to learn how to
perform this mechanism. Thank you, will rate asap
Two Step Reaction 1. What reagent(s) would you use in the first step? 2. Draw the proposed intermediate product. 3. What reagent(s) would you use in the second step? 4. Draw the complete mechanism from the starting reactant to the end product
Please show every step and write clearly. I want to learn how to perform this mechanism....
Please show every step and write clearly. I want to learn how
to perform this mechanism. Thank you, will rate asap
Two Step Reaction 1. What reagent(s) would you use in the first step? 2. Draw the proposed intermediate product. 3. What reagent(s) would you use in the second step? 4. Draw the complete mechanism from the starting reactant to the end product
please answer all the questions. I want to learn how to answer this question properly. thank...
please answer all the questions. I want to learn how to answer
this question properly. thank you, I will rate asap.
Two Step Reaction COOH 1. What reagent(s) would you use in the first step? 2. Draw the proposed intermediate product. 3. What reagent(s) would you use in the second step? 4. Draw the complete mechanism from the starting reactant to the end product
2. Complete the El reaction and answer the following questions. Reagent: Major El product: AH>O a....
2. Complete the El reaction and answer the following questions. Reagent: Major El product: AH>O a. Draw a mechanism of the reaction above. b. Draw an energy diagram of the reaction. Provide the structures of the starting material, intermediates product, and all transition states.
Specify the reagent you would use in each step of the following synthesis: step 1 step...
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 CHCH3 Reagents Available a. LiAlH4 b. H2SO4 f. PBrz 9. pyridinium chlorochromate (PCC) h. Nah c. HCI K. CH3CH2MgBr I. CHgMgBr (phenylmagnesium bromide) m. (CH3)2CHMOBI n. Cro3 d. HB i. NaOH e. SOCI j. CH3 MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 A(C4H100) reacts with phosphorus tribromide to give B(C4H,Br). B...
Specify the reagent you would use in each step of the following synthesis: step 1 step...
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
This is for Organic II. Thank you! write a plausible step-by-step mechanism to illustrate how the reaction would pr...
This is for Organic II. Thank you!
write a plausible step-by-step mechanism to illustrate how the reaction would progress from starting materials to product. 1) NaOH, H20 2) H30C), heat OC2Hs CH2CHS OCH3 1) Na M N MON, 20 NaOH, M,0 M COOH соон
Map.com C,H,COCH, 1.NaBH, > ? 2.H,O+ Add curved arrows to show the mechanism of the first...
Map.com C,H,COCH, 1.NaBH, > ? 2.H,O+ Add curved arrows to show the mechanism of the first step of the reaction. Draw the charged organic intermediate product. Include nonbonding electrons and charges. Omit the counterion. click to edit Nath—B—H → continued below Draw the final product. * continued from above
For questions 1-4, provide the missing reactant(s), reagent(s), or major organic product(s) of each reaction. Only...
For questions 1-4, provide the missing reactant(s), reagent(s), or major organic product(s) of each reaction. Only one type of species is missing for each reaction. If you are providing reactant(8) or product(s), be sure to indicate stereochemistry if it is relevant. If you are providing reagents and more than one step is required, be sure to number each step. 1. EtMgBr 2.H20 NH [H] 5. Propose an efficient synthesis for one of the following transformations. Please circle the synthesis you...
Solve this problem To identify a limiting reagent problem >Amounts (mol, g, etc.) for two different...
Solve this problem
To identify a limiting reagent problem >Amounts (mol, g, etc.) for two different reactants (reactants) are given. Example: Consider the balanced equation shown below. If 2.0 mol RuCl, is reacted with 5.0 mol Li,S, how many moles of Ru,S, can be formed? How many moles of which reagent are left? Step 1: Convert both reactants to moles of the same product. Step 2: Identify the limiting reagent by comparing moles of product determined in Step 1. The...
Please show every step and write clearly. I want to learn how to
perform this mechanism. Thank you, will rate asap
Two Step Reaction 1. What reagent(s) would you use in the first step? 2. Draw the proposed intermediate product. 3. What reagent(s) would you use in the second step? 4. Draw the complete mechanism from the starting reactant to the end product
Please show every step and write clearly. I want to learn how
to perform this mechanism. Thank you, will rate asap
Two Step Reaction 1. What reagent(s) would you use in the first step? 2. Draw the proposed intermediate product. 3. What reagent(s) would you use in the second step? 4. Draw the complete mechanism from the starting reactant to the end product
please answer all the questions. I want to learn how to answer
this question properly. thank you, I will rate asap.
Two Step Reaction COOH 1. What reagent(s) would you use in the first step? 2. Draw the proposed intermediate product. 3. What reagent(s) would you use in the second step? 4. Draw the complete mechanism from the starting reactant to the end product
2. Complete the El reaction and answer the following questions. Reagent: Major El product: AH>O a. Draw a mechanism of the reaction above. b. Draw an energy diagram of the reaction. Provide the structures of the starting material, intermediates product, and all transition states.
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 CHCH3 Reagents Available a. LiAlH4 b. H2SO4 f. PBrz 9. pyridinium chlorochromate (PCC) h. Nah c. HCI K. CH3CH2MgBr I. CHgMgBr (phenylmagnesium bromide) m. (CH3)2CHMOBI n. Cro3 d. HB i. NaOH e. SOCI j. CH3 MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 A(C4H100) reacts with phosphorus tribromide to give B(C4H,Br). B...
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
This is for Organic II. Thank you!
write a plausible step-by-step mechanism to illustrate how the reaction would progress from starting materials to product. 1) NaOH, H20 2) H30C), heat OC2Hs CH2CHS OCH3 1) Na M N MON, 20 NaOH, M,0 M COOH соон
Map.com C,H,COCH, 1.NaBH, > ? 2.H,O+ Add curved arrows to show the mechanism of the first step of the reaction. Draw the charged organic intermediate product. Include nonbonding electrons and charges. Omit the counterion. click to edit Nath—B—H → continued below Draw the final product. * continued from above
For questions 1-4, provide the missing reactant(s), reagent(s), or major organic product(s) of each reaction. Only one type of species is missing for each reaction. If you are providing reactant(8) or product(s), be sure to indicate stereochemistry if it is relevant. If you are providing reagents and more than one step is required, be sure to number each step. 1. EtMgBr 2.H20 NH [H] 5. Propose an efficient synthesis for one of the following transformations. Please circle the synthesis you...
Solve this problem
To identify a limiting reagent problem >Amounts (mol, g, etc.) for two different reactants (reactants) are given. Example: Consider the balanced equation shown below. If 2.0 mol RuCl, is reacted with 5.0 mol Li,S, how many moles of Ru,S, can be formed? How many moles of which reagent are left? Step 1: Convert both reactants to moles of the same product. Step 2: Identify the limiting reagent by comparing moles of product determined in Step 1. The...
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