Why CAN'T the product shown below form under
the reaction conditions used? Explain in words or pictures.
Homework Answers
in this reaction we should substitute OH group in reagent. as we knoe -OH is not good leaving group.
to convert it to leaving group first we should convert -OH to -OTs but such reaction conditions not present.
if reaction is acidic condition then it may leave as H3O but reaction is basic condition so this reaction will not move forward
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Why CAN'T the product shown below form under
the reaction conditions used? Explain in words or...
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...
Fill the table with the products of the reaction of the substrated under each set of...
Fill the table with the products of the reaction of the
substrated under each set of conditions. Assume a work-up at the
end for each reaction. Draw an X through the square of reactions
that would not proceed under the given conditions. (Py = pyridine,
Ac = acetyl)
Assume a work-up at the end for each reaction. Draw an X through the square of reactions that would not proceed under the given conditions. (Py pyridine, Ac acetyl) H2SO4(cat) H20 SOCI2,...
7. Under the following conditions, three products are formed in this reaction. OH H2O a. Draw...
7. Under the following conditions, three products are formed in this reaction. OH H2O a. Draw the mechanism that leads to the product that is the least likely to form in the space below. (7pts) b. In the space below, explain why that product is the most likely to form. You should be able to justify your answer. (4pts)
Assuming the reaction below is under equilibrium conditions, what would help to increase the yield of...
Assuming the reaction below is under equilibrium conditions,
what would help to increase the yield of the product?
Question 10 2.5 pts Assuming the reaction below is under equilibrium conditions, what would help to increase the yield of the product? in high high temp. Product + H2O Product + H20 OH Add water to the reaction Decrease the temperature Remove the carboxylic acid from the reaction Remove water from the reaction Next Previous
Give the major product of the following reaction. -.? HCI OH There is no reaction under...
Give the major product of the following reaction. -.? HCI OH There is no reaction under these conditions or the correct product is not listed. OH Give the major product of the following reaction. HBT H20 OH OH Br There is no reaction under these conditions or the correct product is not listed here. Give the product of the following reaction. to..? OH There is no reaction under these conditions or the correct product is not listed. ОН We were...
Which reaction conditions would you use to perform the reaction shown below? HO CHE O 1....
Which reaction conditions would you use to perform the reaction shown below? HO CHE O 1. BH3, THE 2. H2O2, OH, H20 O 1. Oso 2. NaHSO3 H2O 1.03 2. Zn/H20 or DMS 1. Hg(OAC)2, H20 2. NaBH4
Complete the following reaction equations. Explain product formation and conditions. 900 00-00-00 ho H.POS 1- CI...
Complete the following reaction equations. Explain product formation and conditions. 900 00-00-00 ho H.POS 1- CI H20 H2SO4 Q三文 “o-S
2. A reaction discussed in class involved treating a primary amine with chloroform under basic! conditions to...
2. A reaction discussed in class involved treating a primary amine with chloroform under basic! conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC + CHCIE RNH2 + Lº amine RỌNH 2° amine HANR2 2. A reaction discussed in class involved treating a primary amine with chloroform under basic conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC...
in each reaction box place the best reagent and conditions from the list below. epoxide
In each reaction box, place the best reagent and conditions from
the list below.
Hint : The product is an epoxide, so work backwards to determine
the intermediate and reagents. A peracid (such as mCPBA) is not
available here, so what other method do you know to form epoxides?
What reagent and starting material must be used to form this key
intermediate? For the epoxide formation, consider the basicity and
nucleophilicity of the base.
Sapling Learning macmillan learning In each...
2. Explain why cycloheptatriene, shown below, will react with an acid to form a carbocation (the...
2. Explain why cycloheptatriene, shown below, will react with an acid to form a carbocation (the tropyllum ion)? 3. Predict the major organic product in the following reaction HBT 4. What is the major product of the following reaction? OH HINO, TO CHÚCH . 5. What is the major product of the following reaction? ME E1,0 2)H,09 6. We learned that the bond dissociation ener() of the highlighted C-H bond in toluene is lower than the DE of the C-H...
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...
Fill the table with the products of the reaction of the
substrated under each set of conditions. Assume a work-up at the
end for each reaction. Draw an X through the square of reactions
that would not proceed under the given conditions. (Py = pyridine,
Ac = acetyl)
Assume a work-up at the end for each reaction. Draw an X through the square of reactions that would not proceed under the given conditions. (Py pyridine, Ac acetyl) H2SO4(cat) H20 SOCI2,...
7. Under the following conditions, three products are formed in this reaction. OH H2O a. Draw the mechanism that leads to the product that is the least likely to form in the space below. (7pts) b. In the space below, explain why that product is the most likely to form. You should be able to justify your answer. (4pts)
Assuming the reaction below is under equilibrium conditions,
what would help to increase the yield of the product?
Question 10 2.5 pts Assuming the reaction below is under equilibrium conditions, what would help to increase the yield of the product? in high high temp. Product + H2O Product + H20 OH Add water to the reaction Decrease the temperature Remove the carboxylic acid from the reaction Remove water from the reaction Next Previous
Give the major product of the following reaction. -.? HCI OH There is no reaction under these conditions or the correct product is not listed. OH Give the major product of the following reaction. HBT H20 OH OH Br There is no reaction under these conditions or the correct product is not listed here. Give the product of the following reaction. to..? OH There is no reaction under these conditions or the correct product is not listed. ОН We were...
Which reaction conditions would you use to perform the reaction shown below? HO CHE O 1. BH3, THE 2. H2O2, OH, H20 O 1. Oso 2. NaHSO3 H2O 1.03 2. Zn/H20 or DMS 1. Hg(OAC)2, H20 2. NaBH4
Complete the following reaction equations. Explain product formation and conditions. 900 00-00-00 ho H.POS 1- CI H20 H2SO4 Q三文 “o-S
2. A reaction discussed in class involved treating a primary amine with chloroform under basic! conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC + CHCIE RNH2 + Lº amine RỌNH 2° amine HANR2 2. A reaction discussed in class involved treating a primary amine with chloroform under basic conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC...
In each reaction box, place the best reagent and conditions from
the list below.
Hint : The product is an epoxide, so work backwards to determine
the intermediate and reagents. A peracid (such as mCPBA) is not
available here, so what other method do you know to form epoxides?
What reagent and starting material must be used to form this key
intermediate? For the epoxide formation, consider the basicity and
nucleophilicity of the base.
Sapling Learning macmillan learning In each...
2. Explain why cycloheptatriene, shown below, will react with an acid to form a carbocation (the tropyllum ion)? 3. Predict the major organic product in the following reaction HBT 4. What is the major product of the following reaction? OH HINO, TO CHÚCH . 5. What is the major product of the following reaction? ME E1,0 2)H,09 6. We learned that the bond dissociation ener() of the highlighted C-H bond in toluene is lower than the DE of the C-H...
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