Orthode is a term used in chemistry to describe a hydrocarbon molecule that has a pair of substituent groups attached to adjacent carbon atoms in an aromatic ring. Ortho is derived from the Greek word "orthos," which means straight or correct. The term orthode is often used in the context of organic synthesis and chemical reactions involving aromatic compounds.
Orthode compounds are important intermediates in many chemical reactions, including the synthesis of dyes, drugs, and other organic compounds. They can be synthesized using a variety of methods, including direct substitution reactions, Friedel-Crafts reactions, and cross-coupling reactions.
Orthode compounds often have unique physical and chemical properties, such as increased reactivity, increased acidity, and altered solubility. They can also exhibit enhanced biological activity, such as increased pharmacological potency.
Some examples of orthode compounds include ortho-nitrophenol, ortho-phenylenediamine, and ortho-toluidine. These compounds are used in a variety of industrial and commercial applications, such as the production of plastics, synthetic fibers, and pharmaceuticals.
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