If you like us, please share us on social media or tell your professor. Consider building or adopting a Wikitext for your course like Prof. Dianne Bennett from Sacramento City College demonstrates in this video.

ChemWiki: The Dynamic Chemistry Hypertext > Core > Organic Chemistry > Organic Chemistry With a Biological Emphasis > Chapter 17: Radical reactions

Chapter 17: Radical reactions

Section 17.1: Structure and reactivity of radical species

  1. The geometry and relative stability of carbon radicals.
  2. The diradical character of triplet oxygen

Section 17.2: Radical chain reactions

  1. The three phases of radical chain reactions
  2. Radical halogenation in the lab
  3. Useful polymers formed by radical chain reactions
  4. Destruction of the ozone layer by CFC radicals
  5. Harmful radical species in cells and natural antioxidants

Section 17.3: Enzymatic reactions with free radical intermediates

  1. Hydroxylation of alkanes
  2. Reductive dehydroxylation of alcohols
  3. Radical mechanisms for flavin-dependent reactions 

Section 17.P Problems for Chapter 17


Beginning with acid-base reactions and continuing though the chapters on nucleophilic substitution, carbonyl addition, acyl transfer, carbanion intermediate, and electrophilic mechanisms, we have studied reaction mechanisms in which both electrons in a covalent bond or lone pair move in the same direction. 


In this chapter, we will learn about some reactions in which the key steps involve the movement of single electrons.  You may recall from way back in section 6.1A that single electron movement is depicted by a single-barbed'fish-hook' arrow (as opposed to the familiar double-barbed arrows that we have been using throughout the book to show two-electron movement). 


Single-electron mechanisms involve the formation and subsequent reaction of free radical species, highly unstable intermediates that contain an unpaired electron.  We will learn in this chapter how free radicals are often formed from homolytic cleavage, an event where the two electrons in a breaking covalent bond move in opposite directions.


(In contrast, essentially all of the reactions we have studied up to now involve bond-breaking events in which both electrons move in the same direction: this is called heterolytic cleavage).

We will also learn that many single-electron mechanisms take the form of a radical chain reaction, in which one radical causes the formation of a second radical, which in turn causes the formation of a third radical, and so on.


The high reactivity of free radical species and their ability to initiate chain reactions is often beneficial - we will learn in this chapter about radical polymerization reactions that form useful materials such as plexiglass and polyproylene fabric. We will also learn about radical reactions that are harmful, such as the degradation of atmospheric ozone by freon, and the oxidative damage done to lipids and DNA in our bodies by free radicals species.  Finally, we will see how some enzymes use bound metals to catalyze high energy-barrier reactions - such as alkane hydroxylation or alcohol dehydroxylation - through single-electron steps with radical intermediates.



You must to post a comment.
Last modified
08:28, 2 Oct 2013



(not set)
Lower Divisional






This material is based upon work supported by the National Science Foundation under Grant Numbers 1246120, 1525057, and 1413739.

Creative Commons License Unless otherwise noted, content in the UC Davis ChemWiki is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 United States License. Permissions beyond the scope of this license may be available at copyright@ucdavis.edu. Questions and concerns can be directed toward Prof. Delmar Larsen (dlarsen@ucdavis.edu), Founder and Director. Terms of Use