![1. Alcohol [1] is added to an aqueous solution of sulfuric acid, H,SO4. The solution was then heated. The product was purifie](http://img.homeworklib.com/questions/3535d070-2a7d-11eb-b398-c7426fd81973.png?x-oss-process=image/resize,w_560)
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1. Alcohol [1] is added to an aqueous solution of sulfuric acid, H,SO4. The solution was...
B. Determine the major product of part A. Explain. 2. Consider the following reaction. A. Draw...
B. Determine the major product of part A. Explain.
2. Consider the following reaction. A. Draw the mechanism of the reaction to predict All constitutional products. Show all bonds being made and broken. Show all steps with curved arrows that are necessary to form the products. :B: H H.
CECH HO, H,SO4 HgSO4 Alkynes do not react directly with aqueous acid as do alkenes, but...
CECH HO, H,SO4 HgSO4 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The cnol immediately rearranges to a more stable ketone...
16 Question (1 point) In the presence of sulfuric acid, this alcohol is dehydrated to form...
16 Question (1 point) In the presence of sulfuric acid, this alcohol is dehydrated to form a pair of alkenes through an E1 mechanism. Draw either of the major alkene products of this reaction. H2SO4, heat n 1980. hout ОН
10. Reacting alcohol A with sulfuric acid yields product B with chemical formula CeH6 The H...
10. Reacting alcohol A with sulfuric acid yields product B with chemical formula CeH6 The H NMR for product B is provided below, Provide the structure of productB and use curved arrows to show the mechanism for its formation. (10 points) он H2SO A B (C Hse) H NMR for Compound B 6H 6H 4H 2 PPM
1)Draw all alkene prodcuts that could form 2) Circle the major alkene product expected 3) Draw...
1)Draw all alkene prodcuts that could form
2) Circle the major alkene product expected
3) Draw a complete arrow pushing mechanism how the major
product is formed. (Show all srrows, intermediate structures,
formal charges)
2. (19pts) The alcohol dehydration product below is of the El type elimination. (i) Draw all of the alkene products that could possibly form. (ii) Circle the major alkene product expected. (ii) Draw a complete curved arrow-pushing mechanism illustrating how the major product is formed. Be...
Complete the electron-pushing mechanism for the E1 reaction when 2-methylbutan-2-ol is treated with 20% sulfuric acid....
Complete the electron-pushing mechanism for the E1 reaction when
2-methylbutan-2-ol is treated with 20% sulfuric acid.
Use two curved arrows to show the fast protonation of the alcohol. Use a curved arrow to show the dissociation of the leaving group from the substrate. Draw the organic product of the E1 dehydration Use two curved arrow to show the deprotonation of the carbocation intermediate.
For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in...
For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H, SO4, then draw the structure of the major product of the elimination. ОН H2SO4 - product Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation the carbocation intermediate. Note: HSOZ is formed from step 1, but not shown. Select Draw Rings More Erase Select...
Complete the electron-pushing mechanism for the E1 reaction when 2-methylbutan-2-ol is treated with 20% sulfuric acid....
Complete the electron-pushing mechanism for the E1 reaction when
2-methylbutan-2-ol is treated with 20% sulfuric acid.
Hint: The E1 mechanism involves dissociation of the hydroxyl
group from the substrate. The acid is used to convert the hydroxyl
group to a good leaving group. Do not delete any pre-drawn
bonds/charges/lone pairs.
Complete the electron-pushing mechanism for the E1 reaction when 2-methylbutan-2-ol is treated with 20% sulfuric acid Map a) Use two curved arrows to show the fast b) Use a curved...
Draw the curved arrow mechanims for the reactions of but-1-yne with catalytic trifilic acid in water...
Draw the curved arrow mechanims for the reactions of but-1-yne
with catalytic trifilic acid in water to form butan-2-one,
I just can't seem to figure out the last step! Thank you in
advance!
Draw the curved arrow mechanism for the reaction of but-1-yne with catalytic triflic acid in water to form butan-2-one. Follow the instructions under the boxes for each step. Draw all electrons and charges if necessary on all structures, do not show any inorganic side products Add any...
For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in...
For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H, SO4, then draw the structure of the major product of the elimination. OH to selectivacain intermediate in the prese H2SO4 - product Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation of the carbocation intermediate. Note: HSO, is formed from step 1, but not...
B. Determine the major product of part A. Explain.
2. Consider the following reaction. A. Draw the mechanism of the reaction to predict All constitutional products. Show all bonds being made and broken. Show all steps with curved arrows that are necessary to form the products. :B: H H.
CECH HO, H,SO4 HgSO4 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The cnol immediately rearranges to a more stable ketone...
16 Question (1 point) In the presence of sulfuric acid, this alcohol is dehydrated to form a pair of alkenes through an E1 mechanism. Draw either of the major alkene products of this reaction. H2SO4, heat n 1980. hout ОН
10. Reacting alcohol A with sulfuric acid yields product B with chemical formula CeH6 The H NMR for product B is provided below, Provide the structure of productB and use curved arrows to show the mechanism for its formation. (10 points) он H2SO A B (C Hse) H NMR for Compound B 6H 6H 4H 2 PPM
1)Draw all alkene prodcuts that could form
2) Circle the major alkene product expected
3) Draw a complete arrow pushing mechanism how the major
product is formed. (Show all srrows, intermediate structures,
formal charges)
2. (19pts) The alcohol dehydration product below is of the El type elimination. (i) Draw all of the alkene products that could possibly form. (ii) Circle the major alkene product expected. (ii) Draw a complete curved arrow-pushing mechanism illustrating how the major product is formed. Be...
Complete the electron-pushing mechanism for the E1 reaction when
2-methylbutan-2-ol is treated with 20% sulfuric acid.
Use two curved arrows to show the fast protonation of the alcohol. Use a curved arrow to show the dissociation of the leaving group from the substrate. Draw the organic product of the E1 dehydration Use two curved arrow to show the deprotonation of the carbocation intermediate.
For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H, SO4, then draw the structure of the major product of the elimination. ОН H2SO4 - product Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation the carbocation intermediate. Note: HSOZ is formed from step 1, but not shown. Select Draw Rings More Erase Select...
Complete the electron-pushing mechanism for the E1 reaction when
2-methylbutan-2-ol is treated with 20% sulfuric acid.
Hint: The E1 mechanism involves dissociation of the hydroxyl
group from the substrate. The acid is used to convert the hydroxyl
group to a good leaving group. Do not delete any pre-drawn
bonds/charges/lone pairs.
Complete the electron-pushing mechanism for the E1 reaction when 2-methylbutan-2-ol is treated with 20% sulfuric acid Map a) Use two curved arrows to show the fast b) Use a curved...
Draw the curved arrow mechanims for the reactions of but-1-yne
with catalytic trifilic acid in water to form butan-2-one,
I just can't seem to figure out the last step! Thank you in
advance!
Draw the curved arrow mechanism for the reaction of but-1-yne with catalytic triflic acid in water to form butan-2-one. Follow the instructions under the boxes for each step. Draw all electrons and charges if necessary on all structures, do not show any inorganic side products Add any...
For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H, SO4, then draw the structure of the major product of the elimination. OH to selectivacain intermediate in the prese H2SO4 - product Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation of the carbocation intermediate. Note: HSO, is formed from step 1, but not...
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