toluic Antonyms
No Synonyms and anytonyms found
Meaning of toluic
toluic (a.)
Pertaining to, or designating, one of three metameric acids, CH3.C6H4.CO2H, which are related to toluene and analogous to benzoic acids. They are white crystalline substances, and are called respectively orthotoluic acid, metatoluic acid, and paratoluic acid.
toluic Sentence Examples
- The toluic acid present in the solution was found to have a high purity level.
- Ortho-toluic acid is commonly used as an intermediate in the production of phthalic anhydride.
- The chemical structure of toluic acid consists of a benzene ring with a carboxylic acid group attached to the toluene moiety.
- Meta-toluic acid is less reactive than its ortho and para isomers due to the steric hindrance caused by the methyl group.
- Toluic acid derivatives are employed in the manufacture of dyes, pigments, and pharmaceuticals.
- The solubility of toluic acid in water is influenced by temperature, with higher temperatures leading to increased solubility.
- Para-toluic acid is mainly used as a precursor for the synthesis of terephthalic acid, which is a raw material for polyester fibers.
- The photochemical reaction of toluic acid can result in the formation of benzyl radicals and other intermediates.
- Toluic acid esters display various properties, including solvent resistance and plasticizing effects.
- The corrosion resistance of certain metals can be enhanced by the application of coatings containing toluic acid derivatives.
FAQs About the word toluic
Pertaining to, or designating, one of three metameric acids, CH3.C6H4.CO2H, which are related to toluene and analogous to benzoic acids. They are white crystall
No synonyms found.
No antonyms found.
The toluic acid present in the solution was found to have a high purity level.
Ortho-toluic acid is commonly used as an intermediate in the production of phthalic anhydride.
The chemical structure of toluic acid consists of a benzene ring with a carboxylic acid group attached to the toluene moiety.
Meta-toluic acid is less reactive than its ortho and para isomers due to the steric hindrance caused by the methyl group.
