Turpentine is a solvent obtained by the distillation of pine tree resin It is composed of terpenes, mainly alpha-pinene and beta-pinene.
It is crystalline solid which can be derived from Alpha Pinene. There is various stage of reactions as Alpha Pinene to Camphene then Camphene to Iso Borneol and then IBA to Borneol and Finally Camphor. Regards Dr. Bilson Shukla (bilsonusa@gmail.com)
The phytochemical anethol, alpha-pinene, fenchone, limonene, camphene.
Essential oil, anethole and creosol, alpha-pinene, dianethole, and photoanethole.
This compound is alpha-pinene and is a natural product extracted from coniferous oil.;
Vix smells like alpha pinene, the very same substance that makes pine trees smell so good.
Carvacrol, gamma-terpinene, p-cymene, alpha-pinene, myrcene, thymol, flavanoids, caffeic acid derivatives.
Pinene (C10H16) is a bicyclic monoterpene chemical compound.
Camphor can be produced from alpha-pinene, which is abundant in the oils of coniferous trees and can be distilled from turpentine produced as a side product of chemical pulping. With acetic acid as the solvent and with catalysis by a strong acid, alpha-pinene readily rearranges into camphene, which in turn undergoes Wagner-Meerwein rearrangement into the isobornyl cation, which is captured by acetate to give isobornyl acetate. Hydrolysis into isoborneol followed by oxidation gives racemiccamphor. By contrast, camphor occurs naturally as D-camphor, the (R)-enantiome
C10H16
It is a compound that has a non superimposable mirror image, and an asymmetric center.
I'm not sure what you mean by "peculiar". Amino acids are formed by an amino group, a carboxyl group, a central (linking) carbon, and a variable side group. The side group determines the distinctive amino acid.