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3. For each reaction, give all reasonable products (both ortho and para, for example, f both...
20. Pleas show both ortho and para products (if applicable) a. What type of reaction is...
20. Pleas show both ortho and para products (if applicable)
a. What type of reaction is this? Acylation or alkylation?
b. What type of reaction is this? nitration or halogenation?
c. What type of reaction is this? nitration or
halogenation?
3 20. (EAS - Please sh Please show both ortho and para products,if applicable) What type of reaction is this? nitration or halogenation. CH,CI Cl2/FeCl3 HNO3/H2SO4 AICI What type of reaction is this? acylation or alkylation. What type of reaction...
Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You...
Give a reasonable synthesis for
each of the following compounds from the indicated starting
materials. You may use any other organic or inorganic reagents you
wish unless otherwise indicated. The desired product for each
reaction you propose must be the one of the predominant products.
Give the reactants, conditions (where appropriate) and products of
each synthetic step. If equal mixtures are anticipated (i.e. ortho
/ para products) then indicate where separations are needed. NO
MECHANISMS! [6 points
2. Give a...
4 (6 pts) For each of the following compounds, indicate which statement (A-E) best describes the...
4 (6 pts) For each of the following compounds, indicate which statement (A-E) best describes the reactivity of the benzene ring in electrophilic aromatic substitution reactions (e.g., nitration). A. The ortbo and para positions are activated and the meta position is deactivated. C. The ortho and para positions are deactivated and the meta position is activated. A. All positions are activated -ortho and para are more activated than meta. D. All positions are deactivated -ortbo and para are more deactivated...
please explain why the answer is the answer step by step Retrosynthetic Analysis Give a reasonable...
please explain why the answer is the answer step by step
Retrosynthetic Analysis Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (ie. ortho/para products) then indicate...
Q8-(A-H) These are Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learnt in OChem-1 and OChem-ll. Show all the reagents y...
Q8-(A-H) These are Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learnt in OChem-1 and OChem-ll. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a racemic mixture is formed mark the chiral center with an asterisk () and write "racemic" next to the two structures. All carbon...
3 pts Predict the major product(s) of the following reaction. Select all that apply. If a...
3 pts Predict the major product(s) of the following reaction. Select all that apply. If a reaction would yield both ortho and para products, select both answers. HNO3 H2SO4 Product NO2 ON ON NO2 А B с D B А No Reaction. The reaction would not give a product. Ос OD Rank the substituted benzene molecules in order from 1 - most activated to 5 - least activated (most deactivated) towards electrophilic aromatic substitution. OH CF3 он Br A B...
Please be detailed and give examples used in life. Topic Discuss "Ortho, Para, and Meta Nature of Benzene Deriv...
Please be detailed and give examples used in life.
Topic Discuss "Ortho, Para, and Meta Nature of Benzene Derivatives" by giving at least one example for each type. Your explanation should include relevant mechanisms and references to actual uses in life. A Quality Response Your responses should be a minimum of three posts and it should address all criteria in the rubric below: Your initial response should address the question in the Topic question. It should be substantial and follow...
give the most resonable major product for each reaction #covid-19ruinedschool 3. Give the most reasonable major...
give the most resonable major product for each reaction
#covid-19ruinedschool
3. Give the most reasonable major product for each reaction. For each reaction, write at least one full sentence explaining why the product you chose is formed/what is going on in that reaction. Label each group in each starting material with the terms "electron-donating group" or "electron-withdrawing group." 1 equiv. AICI: onbons SO3 H2SO4
2. D type and strength of each substituents as activating(A) or outcome as ortho-para (O/P) or...
2. D type and strength of each substituents as activating(A) or outcome as ortho-para (O/P) or meta(M) directors. (6 pts) you expect an electrophile to be attached to the ring You must identify the deactivating(D) and also the expected regiochemical 3. Use aromatic, non aromatic or antiaromatic concepts to explain the reactions or molecules shown (6 pts) Provide a curved arrow mechanism to show the formation of a aromatic carbocation intermediate Show the final product H-I The pK,values for the...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as either a 1,2 or 1,4 addition product. b. Write either "thermodynamic" or "kinetic" underneath each one. c. Draw the two resonance structures for the intermediate from which both form H-Br ton nroducts for the following reaction. Draw the the major product or products for the following reaction. Drow the resonance structures for the intermediate from which both form Bra/ hv NBS/ peroxides 11. Give...
20. Pleas show both ortho and para products (if applicable)
a. What type of reaction is this? Acylation or alkylation?
b. What type of reaction is this? nitration or halogenation?
c. What type of reaction is this? nitration or
halogenation?
3 20. (EAS - Please sh Please show both ortho and para products,if applicable) What type of reaction is this? nitration or halogenation. CH,CI Cl2/FeCl3 HNO3/H2SO4 AICI What type of reaction is this? acylation or alkylation. What type of reaction...
Give a reasonable synthesis for
each of the following compounds from the indicated starting
materials. You may use any other organic or inorganic reagents you
wish unless otherwise indicated. The desired product for each
reaction you propose must be the one of the predominant products.
Give the reactants, conditions (where appropriate) and products of
each synthetic step. If equal mixtures are anticipated (i.e. ortho
/ para products) then indicate where separations are needed. NO
MECHANISMS! [6 points
2. Give a...
4 (6 pts) For each of the following compounds, indicate which statement (A-E) best describes the reactivity of the benzene ring in electrophilic aromatic substitution reactions (e.g., nitration). A. The ortbo and para positions are activated and the meta position is deactivated. C. The ortho and para positions are deactivated and the meta position is activated. A. All positions are activated -ortho and para are more activated than meta. D. All positions are deactivated -ortbo and para are more deactivated...
please explain why the answer is the answer step by step
Retrosynthetic Analysis Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (ie. ortho/para products) then indicate...
Q8-(A-H) These are Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learnt in OChem-1 and OChem-ll. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a racemic mixture is formed mark the chiral center with an asterisk () and write "racemic" next to the two structures. All carbon...
3 pts Predict the major product(s) of the following reaction. Select all that apply. If a reaction would yield both ortho and para products, select both answers. HNO3 H2SO4 Product NO2 ON ON NO2 А B с D B А No Reaction. The reaction would not give a product. Ос OD Rank the substituted benzene molecules in order from 1 - most activated to 5 - least activated (most deactivated) towards electrophilic aromatic substitution. OH CF3 он Br A B...
Please be detailed and give examples used in life.
Topic Discuss "Ortho, Para, and Meta Nature of Benzene Derivatives" by giving at least one example for each type. Your explanation should include relevant mechanisms and references to actual uses in life. A Quality Response Your responses should be a minimum of three posts and it should address all criteria in the rubric below: Your initial response should address the question in the Topic question. It should be substantial and follow...
give the most resonable major product for each reaction
#covid-19ruinedschool
3. Give the most reasonable major product for each reaction. For each reaction, write at least one full sentence explaining why the product you chose is formed/what is going on in that reaction. Label each group in each starting material with the terms "electron-donating group" or "electron-withdrawing group." 1 equiv. AICI: onbons SO3 H2SO4
2. D type and strength of each substituents as activating(A) or outcome as ortho-para (O/P) or meta(M) directors. (6 pts) you expect an electrophile to be attached to the ring You must identify the deactivating(D) and also the expected regiochemical 3. Use aromatic, non aromatic or antiaromatic concepts to explain the reactions or molecules shown (6 pts) Provide a curved arrow mechanism to show the formation of a aromatic carbocation intermediate Show the final product H-I The pK,values for the...
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as either a 1,2 or 1,4 addition product. b. Write either "thermodynamic" or "kinetic" underneath each one. c. Draw the two resonance structures for the intermediate from which both form H-Br ton nroducts for the following reaction. Draw the the major product or products for the following reaction. Drow the resonance structures for the intermediate from which both form Bra/ hv NBS/ peroxides 11. Give...
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