Organic Ozonides – How They Form, How They React

Chemistry
As you might guess, organic ozonides may be derived from ozone. So let's first consider the nature of ozone. The ozone molecule, O3 is bent and unstable. It is polarized and is quick to react with unsaturated molecules, notably alkenes and alkynes. The image provided illustrates the result. What, however, is the mechanism producing the result in a typical case?¹ Initially, all three oxygen molecules add to the alkene on the same side of what was previously a double bond. This structure, however, is a transient intermediate, which rearranges to form the ozonide structure. Ozonides are relatively stable. However, they can be readily split to yield a pair of carbonyl compounds. Organic Ozonides in Synthesis Some ozonides are explosive, so they are seldom isolated. However, ozonides can be made to…
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Degrees of Oxidation Using Methane as an Example

Chemistry
One tool of the organic chemist is that of oxidation. There are abundant reagents, which vary in reactivity and strength, to choose from to create this reaction. A plethora of techniques guarantee specificity. All are important to the synthetic organic chemist and to industry. What is a reagent? It is a chemical that is of interest because it can react with the substance chemists wish to modify and study. Oxidizers are one kind of reagent. Consider the progressive oxidation of methane (CH₄) from its lowest to its highest oxidation state. The progression of the oxidation of methane products is written simply, CH₄ → CH₃OH → HCHO → HC(O)OH → HC(O)OOH [→ CO₂ + H₂O ] Their names (left to right) are methane, methyl alcohol, formaldehyde, formic acid, performic acid, and…
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