Please explain clearly why the answer is correct
Answer
Please explain clearly why the answer is correct Which of these "curved arrows" describe a mechanism...
Please explain how you got the answer What are the products implied by the two different mechanistic pathways shown here? PATHWAYA CHCH, - PATHWAY B A + B HECH CHCH CH снен TIT [B] A is II: B is! [E] A is III: B is IV [C] A is l; B is III [A] A is II: B is III [D] A is 1. Bis IV Explanation for your choice (4 pts) Which of these "curved arrows" describe a mechanism...
please explain How many "curved arrows are needed to describe the mechanism for formation of this intermediate? CH [D] 1 (EJ 2 IA 3 IC) 3 [B] 4 Explanation for your choice (3 pts) How can this transformation be accomplished? OH снен A. Br/CCL B. HYPd-C C.O.CH.OH G. HO/acid D. BryH.0 H. BẠH. E. Zn F.H.O I. H-0./NaOH J. CI HO K. NaH L. mCPBA M. HSO/A N. TsCpy O. KMnO/KOH TAJ H then G P. NaOH [B] O then...
Suggest a mechanism using curved arrows and explain clearly the following experimental result. OCH3 CH3OH/H OCH3 75% 25% Show all elecronatiesm for the following reaction. Show all electron flow using curved arrows. H30 (aq) HO OH
Please explain your answer. 12. Redraw the following equations entirely and use the appropriate curved arrows to show bonds breaking/forming. Remember to use the proper type of arrow to show one or two electrons moving! (0.5 pt ea = 1.5 pts) CHEBr – CH3CH2CH2C=ci Na -- CH3CH2CH2CECCH3 + NaBr HEAD CH3OH нысЅн, CH;ge -н H + Hac H3C
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a proton transfer, be sure to include it (them) in your mechanism. (Remember to start by drawing all ionic compounds as ions/drawing out the structure of all reagents, and drawing in all lone pairs.) HCI 3. Which...
Part B (2 of 2) Draw the curved arrows for Step 4 of this mechanism. Arrow-pushing Instructions no -X Step 4 Н IZ H3C -H HC CH Check Next> (2 of 2) Submit Answer Try Another Version 10 item attempts remaining
please help with question 5 part b and show work. thank you!! Draw the curved arrows that accomplish the following transformation: CH HC нс H -CH₂ H-O CH H H.C Closs of a leaving group) Question 5: Predict whether the following carbocation will rearrange, and if so, draw the curved arrow showing the carbocation rearrangement: a) I C-CH₂ сн. I I No rearrangement blc it is already I cancration, which is more stable than I carbocation, b) CH3 CH, CH...
For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any or Ph. NH CI NH Step 1 Correct. This is a nucleophilic attack step. Draw Step 1 of the mechanism. HC H₂C. + NH Edit Cl нс NH CH H
Why the answer is D? Why choice C and E cannot be an answer? It looks so similar to me Can you explain in detail? Also, answer D dosent show any anti or syn addition,,,, Why? please explain all A,B,C,D,E, choices with good explanation Which of the following alkenes reacts fastest with HCI? CH3 Н; Сн A.H.C=CHCH,CH,CH; B.H3C-C-CH=CH, C. a urc=cellence, caren, e. H CH,CH; CHỊ H | CHỊ CHỊCH CH CHH HH D. Alekene can form tertiary carbocation after...
unsure why this is wrong where I put my arrows. please explain Consider the El reaction of the tertiary halide shown. H Н. .Н OH H :Br: Br: NaOH H product Step 1: Add curved arrow(s). Step 2: Add curved arrow(s). Select More Erase Draw Rings More Erase Select Draw Rings C Br H C н Br re Ts e13