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Testdents are trying to synthesize the same ether thatuned two different products Compounds A...
Two students are trying to synthesize the same ether. But they obtained two different products Compounds...
Two students are trying to synthesize the same ether. But they obtained two different products Compounds A & B. CHE 4. points) Give structures for Compounds A & B. 3. ( points) Write mechanisms to account for the formation of each product. Wo Na+ Step one in Bonnie's synthesis is the formation of 1. Na OH Bonnie's Synthesis Bonie's Synthesis 1201 > Compound A 2 CH3) Compound B Bill's Synthesis CH₃O-Net CH30-Na+ 6. (5 points) Which student got it right?
e) Determine the two compounds that can be reacted under basic conditions to synthesize the compound...
e) Determine the two compounds that can be reacted under basic conditions to synthesize the compound whose structure you determined in part (b). (2 points) f) The reaction that is described in part (e) above, when performed, gives a mixture of products and gives poor yield of the product whose structure you determined in part (b). Why? What modifications could you make to the procedure to increase the yield of this product over other side products?2 points)
6). (10 points) Predict the mononitration products of the following compounds. a) o-nitrotoluene b) m-chlorotoluene c)...
6). (10 points) Predict the mononitration products of the following compounds. a) o-nitrotoluene b) m-chlorotoluene c) o-bromobenzoic acid d) p-methoxybenzoic acid e) m-cresol (m-methylphenol) (Two products) (Three products) (Two products) (One product) (Three products) 7). (12 points) Show how you would synthesize the following aromatic derivatives from benzene. You don't have to show mechanisms just show synthesis pathways. a) p-tert-butylnitrobenzene b) p-toluenesulfonic acid c) p-chlorotoluene glad noeg banorte
The following bicyclic compounds give different organic products on treatment with (e) silver(I) salts (note: silver(I)...
The following bicyclic compounds give different organic products on treatment with (e) silver(I) salts (note: silver(I) has a high affinity for halides): OH Br AgNO3 AgBr(s) (- HNO3) OH AgNO3 .Br AgBr(s) (- HNO3) OH Br AgNO3 AgBr(s) (-HNO3) H Give mechanisms for the above reactions that account for the formation of the organic products including their relative stereochemistry. Briefly discuss the driving force and any geometrical requirement for each reaction if any 1םנו
Give the relationship of the two compounds: Different Compounds, Same compound, Constitutional (structural) isomers, Enantiomers, or...
Give the relationship of the two compounds: Different Compounds,
Same compound, Constitutional (structural) isomers, Enantiomers, or
Diastereomers
a) (4 pts) ОН HO- H2C Br H3C b) (4 pts) -OH NH2 NH2 c) (4 pts) OH
Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1:...
Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1: • Predict the products of the following reaction under different temperature conditions. • Show the mechanism for how the two products are formed at different temperatures (include resonance structures if appropriate). • Label the kinetic product and the thermodynamic product. (5 points) -80 °C + HBr 40 °C (2) Predict the product and show the complete mechanism for the following reaction. • Make sure...
Ketone 1 gives two different bicyclic products depending on the base used: when treated with potassium...
Ketone 1 gives two different bicyclic products
depending on the base used: when treated with potassium
tert-butoxide at room temperature, it produces ketone
2, while when treated with LDA at low temperatures
and then heated, it produces ketone 3. Write
arrow-pushing mechanisms for the formation of both
2 and 3 and explain why the
reaction conditions favor each product.
1. KOtBu, tBuOH 1. LDA 2. H2O 2. H2O Br
can you please help with questions 29, 30 and 31? with an explanation 29 Name the following compounds. (6 marks total) а...
can you please help with
questions 29, 30 and 31? with an explanation
29 Name the following compounds. (6 marks total) а) СH; CH3CH2CCH2CH2 OH СH, b) C-NH2 CH,CНСH,- c) CH3CH2CH2CH2CH2CH2- -ОСH,СH-CH, 30 Write a chemical equation for the synthesis of ethyl 2-methylpropanoate. Use structural formulas for each organic compound in your equation. Name each reactant. (6 marks) a) Complete the table below by identifying the types of intermolecular forces in each of the following three-carbon compounds. Note: It is...
•Chemical Ltd upgrades two different end products A and B from the same raw material. •The...
•Chemical Ltd upgrades two different end products A and B from the same raw material. •The products have the same initial processing phase and each have their own further processing phases. •From January’s costs and sales is known: –Raw material costs 13500 kg á 7 €/kg –Initial processing costs in total 44500 € –Product A further processing phase costs 38500 € –Product B further processing phase costs 14 800 € Product A Product B Sales amount 11000 kg 2500 kg...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.)...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
Two students are trying to synthesize the same ether. But they obtained two different products Compounds A & B. CHE 4. points) Give structures for Compounds A & B. 3. ( points) Write mechanisms to account for the formation of each product. Wo Na+ Step one in Bonnie's synthesis is the formation of 1. Na OH Bonnie's Synthesis Bonie's Synthesis 1201 > Compound A 2 CH3) Compound B Bill's Synthesis CH₃O-Net CH30-Na+ 6. (5 points) Which student got it right?
e) Determine the two compounds that can be reacted under basic conditions to synthesize the compound whose structure you determined in part (b). (2 points) f) The reaction that is described in part (e) above, when performed, gives a mixture of products and gives poor yield of the product whose structure you determined in part (b). Why? What modifications could you make to the procedure to increase the yield of this product over other side products?2 points)
6). (10 points) Predict the mononitration products of the following compounds. a) o-nitrotoluene b) m-chlorotoluene c) o-bromobenzoic acid d) p-methoxybenzoic acid e) m-cresol (m-methylphenol) (Two products) (Three products) (Two products) (One product) (Three products) 7). (12 points) Show how you would synthesize the following aromatic derivatives from benzene. You don't have to show mechanisms just show synthesis pathways. a) p-tert-butylnitrobenzene b) p-toluenesulfonic acid c) p-chlorotoluene glad noeg banorte
The following bicyclic compounds give different organic products on treatment with (e) silver(I) salts (note: silver(I) has a high affinity for halides): OH Br AgNO3 AgBr(s) (- HNO3) OH AgNO3 .Br AgBr(s) (- HNO3) OH Br AgNO3 AgBr(s) (-HNO3) H Give mechanisms for the above reactions that account for the formation of the organic products including their relative stereochemistry. Briefly discuss the driving force and any geometrical requirement for each reaction if any 1םנו
Give the relationship of the two compounds: Different Compounds,
Same compound, Constitutional (structural) isomers, Enantiomers, or
Diastereomers
a) (4 pts) ОН HO- H2C Br H3C b) (4 pts) -OH NH2 NH2 c) (4 pts) OH
Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1: • Predict the products of the following reaction under different temperature conditions. • Show the mechanism for how the two products are formed at different temperatures (include resonance structures if appropriate). • Label the kinetic product and the thermodynamic product. (5 points) -80 °C + HBr 40 °C (2) Predict the product and show the complete mechanism for the following reaction. • Make sure...
Ketone 1 gives two different bicyclic products
depending on the base used: when treated with potassium
tert-butoxide at room temperature, it produces ketone
2, while when treated with LDA at low temperatures
and then heated, it produces ketone 3. Write
arrow-pushing mechanisms for the formation of both
2 and 3 and explain why the
reaction conditions favor each product.
1. KOtBu, tBuOH 1. LDA 2. H2O 2. H2O Br
can you please help with
questions 29, 30 and 31? with an explanation
29 Name the following compounds. (6 marks total) а) СH; CH3CH2CCH2CH2 OH СH, b) C-NH2 CH,CНСH,- c) CH3CH2CH2CH2CH2CH2- -ОСH,СH-CH, 30 Write a chemical equation for the synthesis of ethyl 2-methylpropanoate. Use structural formulas for each organic compound in your equation. Name each reactant. (6 marks) a) Complete the table below by identifying the types of intermolecular forces in each of the following three-carbon compounds. Note: It is...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
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