Step1: C-H bond undergo homolytic clevage to produce a methyl radical and hydrogen radical. The formed hydrogen radical combines with Cl radical and produce HCl
Step2: The methyl radical formed reacts with Cl2 molecules and forms a C-Cl bond with abstraction of an electron form Cl2 molecule and produces CH3-Cl and a Cl radical
Although you may not have covered radical reactions yet, the method for adding curved arrows is...
The minor diol product is shown in this synthesis. Draw all missing curved arrows in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. 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.
Complete the mechanism of the following Diels-Alder reaction by drawing the curved arrows for the concerted reaction and the final product formed. (Note that the COOH group is a carboxylic acid group, which is electron withdrawing.) Interactive 3D display mode 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...
Many of the condensations we have studied are reversible. The reverse reactions are often given the prefix retro-, the Latin word meaning “backward.” Propose mechanisms to account for the following reactions. Part B H+ CH3 OH CH (retro-aldol and further condensation) Use H/H2O as your acid/conjugate base. Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron flow arrows should start on the electron(s)...
not sure where I was wrong but need help Course Home <Chapter 10 Homework Alcohol Synthesis Using Organometallic Reagents 5 of 19 > Complete the mechanism by adding curved arrows showing electron flow, and draw the products of the reaction of pentanoic chloride with the first equivalent of the given Grignard reagent before it gets a change to react with the second equivalent. Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the grid and...
Electrophilic Addition Mechanisms of 30 > Formation of alcohol from one touch the hydration of the double bond is the important electrophilic addition on yrion can be accomplished using a variety of reagers Ther m odis hea catalyzed Hydration reaction Look for similares between reaction and the hydrobromation in Port Aand complete them electronegative to lowreas of lower electron density, such as a fydrogen atom or cabocation Use d to werty that the correct w are omgacha bond Draw all...
Model 3: Reactions of Bromine Radical with Various Alkanes For each reaction below, the most likely products are shown. H H H H Rxn I : Br -H H H H H H H H Br H Rxn IV C- H H CHy сн, H,C нC Rxn V BrH н.с CH -сн Critical Thinking Questions 5. Label the carbon radicals in Model 3 as methyl. primary, secondary, tertiary, allyl or benzyl. a) Which carbon radical in Model 3 is closest...