Homework Answers
8.44b3 Get help answering Molecular Drawing questions. Add curved arrow(s) to draw step 3 of the...
8.44b3 Get help answering Molecular Drawing questions. Add curved arrow(s) to draw step 3 of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. СН3 CH, Н.С. CH3 H,C, CH3 Edit Н,0
Practice Problem 13.38b Propose a plausible mechanism for the following transformation. 1) NaH 2) ELI OEt...
Practice Problem 13.38b Propose a plausible mechanism for the following transformation. 1) NaH 2) ELI OEt 13.38b1 Get help answering Molecular Drawing questions Draw the first step of the mechanism, as well as the resulting ion and byproduct that are formed. Note: The tail of each curved arrow must be placed either on a bond or on a lone pair. Make sure to add lone pairs, as necessary, in order to draw the curved arrow(s) properly, and also make sure...
everything is correct except for step 3 i dont know whats wrong Hydrolysis of 2-bromo-2-methylpropane (tert-butyl...
everything is correct except for step 3 i dont know whats
wrong
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 2H,0 → (CH),COH + H,0* + Br Give the Sn1 mechanism. The reactants are already given in step 1: you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count. Note: You...
what am i doing wrong? ULL Help answering Molecular Drawing questions. x) Incorrect. Draw the two...
what am i doing wrong?
ULL Help answering Molecular Drawing questions. x) Incorrect. Draw the two enantiomers that are obtained upon bromination of (S)-3- methylhexane. 0.38 Study. CH3 H2C Edit CH3 Н.С
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
13.57a1 Get help answering Molecular Drawing questions. Add curved arrow(s) to draw step 1 of the...
13.57a1 Get help answering Molecular Drawing questions. Add curved arrow(s) to draw step 1 of the mechanism (using Cl as the X group and H- for the NaBH4). Modify the given drawing of the product as needed to show the intermediate that is formed in this step. Use the single bond tool to interconvert single and double bonds. Edit بل
Practice the Skill 09.16c The following enol cannot be isolated. It rapidly tautomerize to produce ketone....
Practice the Skill 09.16c The following enol cannot be isolated. It rapidly tautomerize to produce ketone. Draw the expected ketone, and show a mechanism for its formation under acid-catalyzed conditions (H30+) Он Part 1 Get help answering Molecular Drawing questions. Draw the missing curved arrow(s) for step one of the mechanism (protonation). Add any missing lone pairs of electrons. он он Edit +H20 SHOW HINT
Complete the mechanism for the generation of the electrophile used for Friedel-Crafts alkylation with the following...
Complete the mechanism for the generation of the electrophile
used for Friedel-Crafts alkylation with the following alkyl halide.
Add curved arrows, bonds, nonbonding electron pairs, and charges
where indicated.
There is a double bond in the 3rd step, but it wont let me create
an arrow from the Iron to the Cl. Can someone explain what I am
doing wrong in the second step? Thanks!
electron pairs, and ch
Complete the mechanism for the generation of the electrophile used for...
i am not sure what i am doing wrong with the curved arrows that are currently present.. Predict the product of the conjugate addition below and then complete the mechanism of the reaction. 0 1...
i
am not sure what i am doing wrong with the curved arrows that are
currently present..
Predict the product of the conjugate addition below and then complete the mechanism of the reaction. 0 1) CH3SH 2) Hao* Complete the mechanism for the conjugate addition by adding the missing curved arrows, bonds, atons es and nonbonding electrons. Use the skeleton provided in each subsequent box to help guide which bonds are formed/broken. o: CHs There is a hint available View...
please answer and label all steps Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (сн), сон +...
please answer and label all steps
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (сн), сон + н,о* + CH CBr 2H,O Br Give the SN1 mechanism. The reactants are already given in step 1; you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count Note: You should have 4 carbon atoms, 13...
8.44b3 Get help answering Molecular Drawing questions. Add curved arrow(s) to draw step 3 of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. СН3 CH, Н.С. CH3 H,C, CH3 Edit Н,0
Practice Problem 13.38b Propose a plausible mechanism for the following transformation. 1) NaH 2) ELI OEt 13.38b1 Get help answering Molecular Drawing questions Draw the first step of the mechanism, as well as the resulting ion and byproduct that are formed. Note: The tail of each curved arrow must be placed either on a bond or on a lone pair. Make sure to add lone pairs, as necessary, in order to draw the curved arrow(s) properly, and also make sure...
everything is correct except for step 3 i dont know whats
wrong
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 2H,0 → (CH),COH + H,0* + Br Give the Sn1 mechanism. The reactants are already given in step 1: you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count. Note: You...
what am i doing wrong?
ULL Help answering Molecular Drawing questions. x) Incorrect. Draw the two enantiomers that are obtained upon bromination of (S)-3- methylhexane. 0.38 Study. CH3 H2C Edit CH3 Н.С
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
13.57a1 Get help answering Molecular Drawing questions. Add curved arrow(s) to draw step 1 of the mechanism (using Cl as the X group and H- for the NaBH4). Modify the given drawing of the product as needed to show the intermediate that is formed in this step. Use the single bond tool to interconvert single and double bonds. Edit بل
Practice the Skill 09.16c The following enol cannot be isolated. It rapidly tautomerize to produce ketone. Draw the expected ketone, and show a mechanism for its formation under acid-catalyzed conditions (H30+) Он Part 1 Get help answering Molecular Drawing questions. Draw the missing curved arrow(s) for step one of the mechanism (protonation). Add any missing lone pairs of electrons. он он Edit +H20 SHOW HINT
Complete the mechanism for the generation of the electrophile
used for Friedel-Crafts alkylation with the following alkyl halide.
Add curved arrows, bonds, nonbonding electron pairs, and charges
where indicated.
There is a double bond in the 3rd step, but it wont let me create
an arrow from the Iron to the Cl. Can someone explain what I am
doing wrong in the second step? Thanks!
electron pairs, and ch
Complete the mechanism for the generation of the electrophile used for...
i
am not sure what i am doing wrong with the curved arrows that are
currently present..
Predict the product of the conjugate addition below and then complete the mechanism of the reaction. 0 1) CH3SH 2) Hao* Complete the mechanism for the conjugate addition by adding the missing curved arrows, bonds, atons es and nonbonding electrons. Use the skeleton provided in each subsequent box to help guide which bonds are formed/broken. o: CHs There is a hint available View...
please answer and label all steps
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (сн), сон + н,о* + CH CBr 2H,O Br Give the SN1 mechanism. The reactants are already given in step 1; you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count Note: You should have 4 carbon atoms, 13...
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