Please predict the outcome of each reaction below:Type you answer as a letter: A, B, ...., or F. Please predict the outcome of each reaction below:Type you answer as a letter: A, B, ..., or F.Problem 1: https://doi.org/10.1021/ol101705jAnswer to Problem 1:Hint 1. Assume the reaction can ONLY occur at the MOST ELECTRON RICH double bond.Hint 2. Assume the reaction can ONLY occur from the least sterically hindered side of the molecule. Draw or build a 3-dimentional conformation to support your answer.1 equivalentm-CPBA?AHBCDEF

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Answered: Please predict the outcome of each…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 42E

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Draw a curved arrow mechanism for the substitution reaction that will occur with the alkyl halide and nucleophile below, adding steps as necessary. Be sure to include all nonbonding electrons and all nonzero formal charges, and show all species that react or are formed in this reaction.
only answer part D. thank you
(in first pic) need help with the last one, with the alkyne & the question in the 2nd pic. thank you!!
Give correct detailed Solution with explanation needed of each steps..don't give Handwritten answer....don't use Ai for answering this
Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.
ited Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. od m... • You do not have to consider stereochemistry. . Do not include anionic counter-ions, e.g., I', in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom Separate resonance structures using the → symbol from the drop-down menu. ● CH4 + ? HBr
1. please answer a and b
Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.
with the corresponding reaction step. Drag and drop options on the right-hand side to swap positions and match with items on the left. Reordering may cause items on the right- hand side to swap positions. A) B) C) D) Loss of leaving group Proton transfer (acid/ base) Nucleophilic attack Rearrangement OH H. A) OH Br Pr Br Et NaBr/H2SO4 Me + HSO4 Na Pri or Me Et Me Et Br Pr © D) Br Η ΘΗ Н B) c) H -H +0==0 OH H + H₂O III III III III
See image below
3) Use the reaction shown below and the associated reaction energy diagram to answer the following questions. E A Но- + Br HO. Br- reaction coordinate a) In the space above, use curved arrows to show the mechanism of the reaction. b) Classify the reaction as either addition, elimination or substitution. c) In this reaction is hydroxide (HO-) acting as a nucleophile or as a base? c) Based on the reaction energy diagram, is the reaction endergonic or exergonic? d) Based on the reaction energy diagram, and assuming the reaction is reversible, would the equilibrium lie to the left or to the right? e) Which position on the reaction energy diagram (A, B or C) corresponds to the transition state?
Give detailed Solution with explanation needed..give correct answer if you not then don't give answer..I will give you upvote..draw out all of the substitution and elimination reactions

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