Outcome 13 - Bridge Assignment 1Free-Radical Polymerization1)Draw the mechanism and products of the below initiation step:hv2)Draw the mechanisms and products for the propagation steps that result in the free-radical halogenation of ethane.H -CC.Cl,3) Draw the mechanisms and products for the propagation steps that result in the free-radical halogenation of carbon#2 of butane.BrBr,Draw the mechanisms and products for one propagation step between a chlorine radical and ethylene. The most4)accessible electrons are the pi-bond electrons!!!!HciH.

1. Peroxide clevege under light results alkoxy radical. 2. Free radical substitution involves…

Outcome 13 - Bridge Assignment 1 Free-Radical Polymerization 1) Draw the mechanism and products of the below initiation step: hv 2) Draw the mechanisms and products for the propagation steps that result in the free-radical halogenation of ethane. %23 3) Draw the mechanisms and products for the propagation steps that result in the free-radical halogenation of carbon #2 of butane. Br Br, 4) Draw the mechanisms and products for one propagation step between a chlorine radical and ethylene. The most accessible electrons are the pi-bond electrons!!!! H H.

Outcome 13 - Bridge Assignment 1 Free-Radical Polymerization 1) Draw the mechanism and products of the below initiation step: hv 2) Draw the mechanisms and products for the propagation steps that result in the free-radical halogenation of ethane. %23 3) Draw the mechanisms and products for the propagation steps that result in the free-radical halogenation of carbon #2 of butane. Br Br, 4) Draw the mechanisms and products for one propagation step between a chlorine radical and ethylene. The most accessible electrons are the pi-bond electrons!!!! H H.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter10: Organohalides

Section10.SE: Something Extra

Problem 18MP: Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions...

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