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Terpenes are classified by the number of carbons: monoterpenes (C 10), sesquiterpenes (C 15), diterpenes (C 20), as examples. The terpene alpha-pinene is a major component of the common solvent, turpentine. The one terpene that has major applications is natural rubber (i.e., polyisoprene).
Terpenoids are modified terpenes, [7] wherein methyl groups have been moved or removed, or oxygen atoms added. Some authors use the term "terpene" more broadly, to include the terpenoids. Just like terpenes, the terpenoids can be classified according to the number of isoprene units that comprise the parent terpene:
Diterpenes are a class of terpenes composed of four isoprene units, often with the molecular formula C 20 H 32. They are biosynthesized by plants, animals and fungi via the HMG-CoA reductase pathway , with geranylgeranyl pyrophosphate being a primary intermediate.
Monoterpenes are a class of terpenes that consist of two isoprene units and have the molecular formula C 10 H 16. Monoterpenes may be linear (acyclic) or contain rings (monocyclic and bicyclic). Modified terpenes, such as those containing oxygen functionality or missing a methyl group, are called monoterpenoids. Monoterpenes and monoterpenoids ...
Rishitin is another example of a cadinene, which is found in potatoes and tomatoes. [6] [7] Vetivazulene and guaiazulene are aromatic bicyclic sesquiterpenoids. With the addition of a third ring, the possible structures become increasingly varied. Examples include longifolene, copaene and the alcohol patchoulol.
An example spangram with corresponding theme words: PEAR, FRUIT, BANANA, APPLE, etc. Need a hint? Find non-theme words to get hints. For every 3 non-theme words you find, you earn a hint.
Hopane: An example of a pentacyclic triterpene Triterpenes are a class of terpenes composed of six isoprene units with the molecular formula C 30 H 48 ; they may also be thought of as consisting of three terpene units.
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