please help me answer both questions Curved arrows are used to illustrate the flow ofelectrons. Using the provided starting and productstructures, draw the curved electron-pushing arrows forthe following reaction or mechanistic step(s).Be sure to account for all bond-breaking and bond-making steps.Drawing Arrows-COHQHH+0HDrag To Pan Curved arrows are used to illustrate the flow of electrons. Use the reactionconditions provided and follow the curved arrows to draw the reactant andproduct of this hydrohalogenation reaction.Include all lone pairs and charges as appropriate.HHDrawingHBr1,2-hydrideshiftBr¯Select to DrawSelect to DrawHQI

Answered: Image /qna-images/answer/b4901a29-0139-4c8c-8101-2052dc36ad83.jpg

Answered: Curved arrows are used to illustrate…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter18: Aromaticity

Section: Chapter Questions

Problem 12E

See similar textbooks

Similar questions

Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the first step of this reaction sequence. Be sure to account for all bond-breaking and bond- making steps. I H BH₂ H B H Select to Add Arrows > H Bll H BH₂
Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond-making steps.
Draw the mechanism and the energy diagram for the reaction shown below. Include any resonance structures for the intermediates of the reaction. H3O+
Shown below is a carbocation intermediate in an electrophilic addition reaction of HCl with an alkene. For the conformation shown, select each hydrogen whose bond to carbon is aligned for effective hyperconjugation with the vacant p orbital on the positively charged carbon. Each adjacent carbon will have only one C-H bond so aligned. • Gray = C; white = H; red = 0; blue = N; dark green = Cl; brown =Br; light green =F; purple = I; yellow = S; orange = P. • Double click to select atoms. • You can zoom in and out using the mouse scroll wheel (or pinch to zoom on touch screens).
See image below
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown HCI - You do not have to consider stereochemistry. -Do not include anionic counter-1ons, e.g., I, in your answer. - Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. - Separate resonance structures using the symbol from the drop-down menu. y自ノ ee P. opy aste [F CH
Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. :0: H HH NaOH, H2O :0: H Na → Select to Add Arrows CH3CH2CH2CH О HH :0: 'H H H HH Na ◉H Select to Add Arrows NaOH, H2O :0: 60• NaOH, H₂O H H HHI I Select to Add Arrows Select to Add Arrows NaOH, H2O H NaOH, H₂O Hi HH Select to Add Arrows > HH :0: H 1 Q
Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Na O Na O co Select to Add Arrows H H H po ² Select to Add Arrows 0:0
Draw both resonance structures of the most stable carbocation ntermediate in the reaction shown. +HBr • You do not have to consider stereochemistry. Do not include anionic counter-1ons, e.g., I, in your answer. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the → symbol from the drop-down menu, P. opy aste C. 000▼[片 vate Windows
2) Provide a detailed mechanism for the addition reaction shown below. State the regiochemistry and explain why it's unusual. Please be sure to include all structures (use line angle notation or perspective diagrams as appropriate to illustrate the stereochemistry of the process), resonance forms, intermkediates, transition states, curved arrows, formal charges, or lone pairs as necessary. Please don't cheat. Br HBr SCH3 SCH + EN
Given the reactant Br−Br, add curved arrows to show homolytic bond cleavage, then draw the expected product. Be sure to add any charges and nonbonding electrons that result from the cleavage.
5. Using curved arrows show the mechanism for the hydrohalogenation for the following reaction. Show how the two possible intermediate products are formed and explain why only one product proceeds to form the product. Clearly indicate attack of electrons and full and partial (8) charges. H-Br Br H-Br Product Intermediate Products

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS