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Question 4: Diagram the following transformation using proper arrow formalism. Then, answer the follow-up questions. 1.)...
1. (4 pts) Rank each of the following carbocations in order of stability (1 most stable...
1. (4 pts) Rank each of the following carbocations in order of stability (1 most stable and 4 least stable). н н сH н Н,с Н,с" H сH; CH3 Hас- H 2. (6 pts total; 2 pts each) Complete the following transformations by indicating the reactant structure or the major organic product(s). Place your answer(s) in the space provided. Be certain to indicate stereochemistry where applicable. Cl2 Он cat. H2SO H-о Br Br conc. HBra) сн сна 3. (10 pts...
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You...
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You do not need to provide any starting material or product, just the reaction conditions (see example below) 1.B Example: Show reagent 'B' followed by aqueous acid: 2. H30 a. Markovnikov addition of H2O to a double bond: b. Anti-Markovnikov addition of H2O to a double bond: c. Markovnikov addition to form an alkyl bromide from an alkene: d. Reaction conditions to change 1,2-dimethylcyclohexene into...
Please completely answer the questions, thank you! For the reactions below, 1. supply the reagents needed...
Please completely answer the questions, thank you!
For the reactions below, 1. supply the reagents needed to carry out the reaction, by writing them above the reaction arrow. 2. Use choices 1A through 11, 2A through 24, and 3A through 3X, above to answer the questions about reaction types and mechanistic details. 3. For the reactions in column 3, that require you to diagram the mechanism, diagram the mechanism. Column 1 Column 2 Column 3 Type of Reaction The Reason...
please answee all 3 pages! they are multiple choice 3. Answer the following questions. Clearly mark...
please answee all 3 pages! they are multiple choice
3. Answer the following questions. Clearly mark your answer. (1 point each: 25 points total) a. Circle the substrate that will give 4 different products when reacted fully under hydroboration-oxidation conditions. b. Circle the substrate that will not result in a tertiary alkyl chloride when treated with HCI. C. Circle the alkene that can be most easily formed under unimolecular elimination d. Circle the alkene that will react fastest with m-chloroperoxybenzoic...
please answer questions 1-4 Question 1 Which of the following is the most stable carbocation? СН3...
please answer questions 1-4
Question 1 Which of the following is the most stable carbocation? СН3 V. CH2 What is the major product of the following reaction? Н HBO C CHS CH CH CH3-CH ( CH, Br CH2-CH-C–CH, Br Br CH CH CH3-CH:-¢-CH Br ін, CHE CH CH.-CH- Br CH. D Question 3 What is the major product of the following reaction? CH, НО 1 Оснок IV. CH2OH CH3 "О" ОН Д. он СН3 CH3 Но Ш. CH, ОН Question...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the experimental section above) H2SO4 + Na2Cr207 2H20- H2O, A Molecular Weight Theoretical yield amount moles on (if applicable) Equivalents 2. Look up the melting point for p-nitrobenzoic acid and record the reference. 3. What color change is expected to be observed in the reaction? Explain why. CHROMIC ACID OXIDATION Experimental Procedure: Part I: Synthesis of p-nitrobenzoic Acid 1. Under the hood, add 0.400 g...
please answer all the questions Question 8 0 / 1 pts Our understanding of RNA ...
please answer all the questions
Question 8
0 / 1 pts
Our understanding of RNA
was non-existent until 2000
started with the identification of a tRNA which suggested a
method of converting DNA to protein
began to identify that DNA-->protein--> RNA
stopped growing after it's original discovery in the 70s
IncorrectQuestion 10
0 / 1 pts
Enzymes allow for chemical reactions to occur in the cell that
may not naturally occur at the right place at...
Question to answer from the lab: What aspect(s) of the approach taken is/are NOT especially green?...
Question to answer from the lab: What aspect(s) of the approach taken is/are NOT especially green? What changes might be made to make the overall process greener? The Lab Experiment Summary Polyethylene glycols such as PEG-400 are currently of great interest to organic chemists, since their application as reaction solvents is very intriguing (1). PEG-400 is non-volatile and nonflammable in nature, and also possesses important properties such as recyclability, ease of work-up, thermal stability and economical cost. In addition, the...
QUESTIONS TO ANSWER: Prepare a table of all chemicals used with the structure and purpose of...
QUESTIONS TO ANSWER:
Prepare a table of all chemicals used with the structure and
purpose of each.
Calculate the theoretical yield by finding limiting reactant of
the experiment by converting reactants to product (remember to show
all calculations used)
Calculate the percent yield using the limiting reactant
Calculate the Rf for triphenylmethanol. If there are two dots,
determine which one is triphenylmethanol.. ( I did not provide
data. Please let me know how I Would do this if I did)...
please help answer question 4, a-f please using the data below from chart 1 objectives from...
please help answer question 4, a-f please
using the data below from chart 1
objectives from lab, thank you
DATA:CA y 3 Ay No3 Part I: Cell Potential of voltaic cells under standard conditions: cell CU CND2 #27 14.0m Give the half Half cell reaction at Combinations Oxidation Reduction E the anode and with [ion] takes place Theoretical takes place cathode. Write in M here here (V) above the arrow E c (V) if it is oxidation or reduction. |-0.340...
1. (4 pts) Rank each of the following carbocations in order of stability (1 most stable and 4 least stable). н н сH н Н,с Н,с" H сH; CH3 Hас- H 2. (6 pts total; 2 pts each) Complete the following transformations by indicating the reactant structure or the major organic product(s). Place your answer(s) in the space provided. Be certain to indicate stereochemistry where applicable. Cl2 Он cat. H2SO H-о Br Br conc. HBra) сн сна 3. (10 pts...
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You do not need to provide any starting material or product, just the reaction conditions (see example below) 1.B Example: Show reagent 'B' followed by aqueous acid: 2. H30 a. Markovnikov addition of H2O to a double bond: b. Anti-Markovnikov addition of H2O to a double bond: c. Markovnikov addition to form an alkyl bromide from an alkene: d. Reaction conditions to change 1,2-dimethylcyclohexene into...
Please completely answer the questions, thank you!
For the reactions below, 1. supply the reagents needed to carry out the reaction, by writing them above the reaction arrow. 2. Use choices 1A through 11, 2A through 24, and 3A through 3X, above to answer the questions about reaction types and mechanistic details. 3. For the reactions in column 3, that require you to diagram the mechanism, diagram the mechanism. Column 1 Column 2 Column 3 Type of Reaction The Reason...
please answee all 3 pages! they are multiple choice
3. Answer the following questions. Clearly mark your answer. (1 point each: 25 points total) a. Circle the substrate that will give 4 different products when reacted fully under hydroboration-oxidation conditions. b. Circle the substrate that will not result in a tertiary alkyl chloride when treated with HCI. C. Circle the alkene that can be most easily formed under unimolecular elimination d. Circle the alkene that will react fastest with m-chloroperoxybenzoic...
please answer questions 1-4
Question 1 Which of the following is the most stable carbocation? СН3 V. CH2 What is the major product of the following reaction? Н HBO C CHS CH CH CH3-CH ( CH, Br CH2-CH-C–CH, Br Br CH CH CH3-CH:-¢-CH Br ін, CHE CH CH.-CH- Br CH. D Question 3 What is the major product of the following reaction? CH, НО 1 Оснок IV. CH2OH CH3 "О" ОН Д. он СН3 CH3 Но Ш. CH, ОН Question...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the experimental section above) H2SO4 + Na2Cr207 2H20- H2O, A Molecular Weight Theoretical yield amount moles on (if applicable) Equivalents 2. Look up the melting point for p-nitrobenzoic acid and record the reference. 3. What color change is expected to be observed in the reaction? Explain why. CHROMIC ACID OXIDATION Experimental Procedure: Part I: Synthesis of p-nitrobenzoic Acid 1. Under the hood, add 0.400 g...
please answer all the questions
Question 8
0 / 1 pts
Our understanding of RNA
was non-existent until 2000
started with the identification of a tRNA which suggested a
method of converting DNA to protein
began to identify that DNA-->protein--> RNA
stopped growing after it's original discovery in the 70s
IncorrectQuestion 10
0 / 1 pts
Enzymes allow for chemical reactions to occur in the cell that
may not naturally occur at the right place at...
QUESTIONS TO ANSWER:
Prepare a table of all chemicals used with the structure and
purpose of each.
Calculate the theoretical yield by finding limiting reactant of
the experiment by converting reactants to product (remember to show
all calculations used)
Calculate the percent yield using the limiting reactant
Calculate the Rf for triphenylmethanol. If there are two dots,
determine which one is triphenylmethanol.. ( I did not provide
data. Please let me know how I Would do this if I did)...
please help answer question 4, a-f please
using the data below from chart 1
objectives from lab, thank you
DATA:CA y 3 Ay No3 Part I: Cell Potential of voltaic cells under standard conditions: cell CU CND2 #27 14.0m Give the half Half cell reaction at Combinations Oxidation Reduction E the anode and with [ion] takes place Theoretical takes place cathode. Write in M here here (V) above the arrow E c (V) if it is oxidation or reduction. |-0.340...
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