unsure why this is wrong where I put my arrows. please
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unsure why this is wrong where I put my arrows. please
explain
Consider the El reaction...
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...
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...
estion 14 of 14 Attemp For the dehydration shown, use curved arrows to show the formation...
estion 14 of 14 Attemp For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H,SOą, then draw the structure of the major product of the elimination. ОН H, SO 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: HSO, is formed from step 1, but not shown. Select Draw...
D esures Hint Chech Question 14 of 14 > Step 1: Use curved arrows to complete...
D esures Hint Chech Question 14 of 14 > 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 shown. Select Draw Rings More Erase Select Draw Rings More Erase CHO 2 Q Step 3: Use a curved arrow to show the carbocation rearrangement. Step 4: Draw curved arrows to show the elimination to...
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, SO2, then draw the structures of the minor and major products of the elimination. H2SO4 - Major and Minor products O 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 for the elimination. Select Draw Rings More Erase Select Draw...
Complete the mechanism for an aldol condensation in base by drawing in the curved arrows where...
Complete the mechanism for an aldol condensation in base by drawing in the curved arrows where needed. Step 1. Generation of enolate nucleophile. Select Draw Rings More o @ 21@ Step 2. Nucleophilic addition of enolate to a carbonyl. Select Draw Rings More Erase Step 3. Generation of B-hydroxyketone. Select Draw Rings More Erase Step 4.Dehydration to a.B-unsaturated ketone. Select Draw Rings More Erase II | A || H > -H
Draw curved arrows to show electron reorganization for the reaction step below ts 2req Visted Arrow-pushing...
Draw curved arrows to show electron reorganization for the reaction step below ts 2req Visted Arrow-pushing Instructions CXm pts pts 2req HO: н 1 pls н о н C=c-H H-: C-C-H Н + + H Н Draw curved arrows to show electron reorganization for the reaction step below. 1 pts 2req w Arrow-pushing Instructions Show.1 pts 1 pls 2req on 1 pls H H H H H EkUView opIca Kelerences Noting the curved arrows, draw all the product(s), organic and...
what am I doing wrong here? Draw curved arrows to show electron reorganization for the reaction...
what am I doing wrong here?
Draw curved arrows to show electron reorganization for the reaction step b Arrow-pushing Instructions H:0 H-OH C C H H HC-C-H 1 more group attempt remaining Retry Entire Group Submit Answer
Please draw the major product for this reaction I drew this and it said it waas...
Please draw the major product for this reaction I drew this and
it said it waas wrong please help, thanks
Conversion of tertiary alcohols to alkenes under acidic conditions involves two cationic intermediates. For the reaction below: OH Hao a Write a mechanism for the step below using curved arrows to show electron reorganization. Arrow-pushing Instructions H Ob Draw the organic product of the mechanism step above Do not include counter-ions, e.g., Na IT, in your answer.
please tell me whats wrong in my answer, Im so confused. Modify the molecule to show...
please tell me whats wrong in my answer, Im so confused.
Modify the molecule to show the products formed by the hydrolysis of tripalmitoylglycerol. Add or remove atoms or bond as needed. Show all hydrogen atoms. Select Draw Rings More Erase VICONH I u H,C - OH Us HC OH HO CH UFU O 1. нс — он HO £ܝ @lala
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...
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...
estion 14 of 14 Attemp For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H,SOą, then draw the structure of the major product of the elimination. ОН H, SO 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: HSO, is formed from step 1, but not shown. Select Draw...
D esures Hint Chech Question 14 of 14 > 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 shown. Select Draw Rings More Erase Select Draw Rings More Erase CHO 2 Q Step 3: Use a curved arrow to show the carbocation rearrangement. Step 4: Draw curved arrows to show the elimination to...
For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H, SO2, then draw the structures of the minor and major products of the elimination. H2SO4 - Major and Minor products O 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 for the elimination. Select Draw Rings More Erase Select Draw...
Complete the mechanism for an aldol condensation in base by drawing in the curved arrows where needed. Step 1. Generation of enolate nucleophile. Select Draw Rings More o @ 21@ Step 2. Nucleophilic addition of enolate to a carbonyl. Select Draw Rings More Erase Step 3. Generation of B-hydroxyketone. Select Draw Rings More Erase Step 4.Dehydration to a.B-unsaturated ketone. Select Draw Rings More Erase II | A || H > -H
Draw curved arrows to show electron reorganization for the reaction step below ts 2req Visted Arrow-pushing Instructions CXm pts pts 2req HO: н 1 pls н о н C=c-H H-: C-C-H Н + + H Н Draw curved arrows to show electron reorganization for the reaction step below. 1 pts 2req w Arrow-pushing Instructions Show.1 pts 1 pls 2req on 1 pls H H H H H EkUView opIca Kelerences Noting the curved arrows, draw all the product(s), organic and...
what am I doing wrong here?
Draw curved arrows to show electron reorganization for the reaction step b Arrow-pushing Instructions H:0 H-OH C C H H HC-C-H 1 more group attempt remaining Retry Entire Group Submit Answer
Please draw the major product for this reaction I drew this and
it said it waas wrong please help, thanks
Conversion of tertiary alcohols to alkenes under acidic conditions involves two cationic intermediates. For the reaction below: OH Hao a Write a mechanism for the step below using curved arrows to show electron reorganization. Arrow-pushing Instructions H Ob Draw the organic product of the mechanism step above Do not include counter-ions, e.g., Na IT, in your answer.
please tell me whats wrong in my answer, Im so confused.
Modify the molecule to show the products formed by the hydrolysis of tripalmitoylglycerol. Add or remove atoms or bond as needed. Show all hydrogen atoms. Select Draw Rings More Erase VICONH I u H,C - OH Us HC OH HO CH UFU O 1. нс — он HO £ܝ @lala
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