Oxidation and Reduction in Organic Chemistry

We’ve pointed out on several occasions that some of the reactions discussed in this and earlier chapters are either oxidations or reductions. An organic oxidation results in a loss of electron density by carbon, caused either by bond formation between carbon and a more electronegative atom (usually O, N, or a halogen) or by bond-breaking between carbon and a less electronegative atom (usually H). Conversely, an organic reduction results in a gain of electron density by carbon, caused either by bond formationbetween carbon and a less electronegative atom or by bond-breaking between carbon and a more electronegative atom.

Based on these definitions, the chlorination reaction of methane to yield chloromethane is an oxidation because a C - H bond is broken and a C - Cl bond is formed. The conversion of an alkyl chloride to an alkane via aG rignard reagent followed by protonation is a reduction, however, because a C - Cl bond is broken and a C - H bond is formed.

As other examples, the reaction of an alkene with Br2 to yield a 1,2-dibromide is an oxidation because two C - Br bonds are formed, but the reaction of an alkene with HBr to yield an alkyl bromide is neither an oxidation nor a reduction because both a C - H and a C - Br bond are formed.

A list of compounds of increasing oxidation level is shown in Figure 1.1.   Alkanes are at the lowest oxidation level because they have the maximum possible number of C - H bonds per carbon, and CO₂ is at the highest levelbecause it has the maximum possible number of C - O bonds per carbon. Any reaction that converts a compound from a lower level to a higher level is an oxidation, any reaction that converts a compound from a higher level to a lower level is a reduction, and any reaction that doesn’t change the level is neither an oxidation nor a reduction.

Figure 1.1 Oxidation levels of some common types of compounds.

مواضيع ذات صلة

Curly arrows are vital for learning organic chemistry

Mechanisms with several steps

Watch out for five-valent carbons

Drawing your own mechanisms with curly arrows

σ bonds as nucleophiles

π bonds as nucleophiles

Charge is conserved in each step of a reaction

Curly arrows show the movement of electrons

Curly arrows represent reaction mechanisms

Identifying an electrophile

Nucleophiles and electrophiles

Orbital overlap is essential for successful reaction