Consider this step in a radical reaction:Brhv?What type of step is this? Check all that apply.Draw the products of the step on the right-hand side of the drawing areabelow. If more than one set of products is possible, draw any set.Also, draw the mechanism arrows on the left-hand side of the drawingarea to show how this happens.initializationelectrophilicpassivationterminationnone of the aboveBrХХClick and drag to startdrawing a structure.0000.Ar☑

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Answered: Consider this step in a radical…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter20: Acidity And Pka Of Phenols

Section: Chapter Questions

Problem 11E

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Draw a mechanism for this reaction. H₂C- CH3 -0- Interactive 3D display mode -CH3 H₂C CH₁₂ H₂C-O i Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be created.
Construct a three-step synthesis of 1-bromopropane from propane by dragging the appropriate formulas into the bins. Note that each bin willl hold only one item, and not all of the given reagents or structures will be used. Reactant Reagent 1 Step 1 Product Reagent 2 Step 2 Product Reagent 3 Final Product (1-bromopropane) (propane) Br2 Br2 (CH)3CO K HBr ROOR HBr NBS ROOR HaC Нас Нас, Нас Нас НаС. hv CH2 CH2 CH Нс CH-Br CH-Br CH Нас Нас, нC Нас НаС Br Br Br
Draw the reactants and complete the mechanism by drawing in the appropriate electron-flow arrows (including stereochemistry) for the following Sy2 reaction of an alkyl bromide. Represent the nucleophile as an ion. Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the grid and connecting them with bonds, including charges where needed. Indicate the mechanism by drawing the electron-flow arrows on the molecules. Arrows should start on an atom or a bond and should end on an atom, bond, or where a new bond should be created. • View Available Hint(s) + CH N H. S CH H,C C-ÖH CI HC Br HC F [1] A
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. ох Br H₂O
4. For the following reaction scheme, please convert the starting material to the corresponding product. If the reaction is destined to fail, please write "no reaction" to the right, otherwise draw the appropriate product to the right of the arrow. NABH4 MeOH 1. LİAIH4 Meo 2. H20 OMe 1. CH3MgBr (excess) 2. H2О 1. C6H5LI (excess) 2. Нао
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4. Please choose either Reaction A or Reaction B, and then provide the complete mechanism. The mechanism MUST include the formation of the "super electrophile." Then provide the reaction coordinate pathway starting from benzene + super electrophile. Be sure to include an energy access and labels for reactants, products, intermediates, energies of activation, and transition states. Reaction A NO2 Reaction B HNO3, H2SO4 CH3COCI, AICI3
Please step by step answer and don't use ASI Answer please
Part 1 Identify any nucleophiles and electrophiles in this reaction. How will they react together? Do all curved arrows start at an electron-rich site and point toward an electron-poor site? Did you add non-zero charges and lone pair electrons to all appropriate atoms? Does the overall charge and number of atoms remain consistent from step-to-step? To bring a box back to its original status, click on the reset button in the top left corner of the drawing window. x i :0:
Part 2: Formation of alcohols with oxygen nucleophiles. The oxygen nucleophiles are water and hydroxide anion. Complete the table below, drawing the structure of the major product and indicating the dominant mechanism (be aware that in some cases, there is no reaction, or reaction is too slow to be effective) HOⓇ Is this a strong base? Is this a good nucleophile? Product from reaction with Product from reaction with Br Product from reaction with Br Br Br Product from reaction with Br Product from reaction with Product from reaction with H₂O
I don't understand what to put for final step. Does that just mean termination? And would a radical form when I add bromine to ch2 between the rings?

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