What is the Difference Between R and S Carvone?
🆚 Go to Comparative Table 🆚Carvone is a member of a family of chemicals called terpenoids and is found naturally in many essential oils, with the highest concentrations in caraway, spearmint, and dill seeds. Carvone forms two mirror-image forms or enantiomers: R-(−)-carvone and S-(+)-carvone. The main differences between R and S carvone are:
- Occurrence: S-(+)-carvone is the principal constituent (60–70%) of caraway seed oil and occurs to the extent of about 40–60% in dill seed oil. R-(−)-carvone is the most abundant compound in the essential oil from several species of mint, particularly spearmint oil, which is composed of 50–80% R-(−)-carvone.
- Odor: R-(−)-carvone has a sweetish minty smell, like spearmint leaves. In contrast, S-(+)-carvone has a slightly different scent due to its mirror-image structure.
- Applications: Both R and S carvone are used in the food and flavor industry. R-(−)-carvone is also used for air freshening products and has been approved by the U.S. Environmental Protection Agency for use as a mosquito repellent. S-(+)-carvone has fewer uses but adds to the flavor of kümmel, a liqueur popular in Europe.
In summary, R and S carvone are enantiomers found in different essential oils, with R carvone primarily occurring in mint oils and S carvone in caraway and dill oils. They have different scents and applications.
Comparative Table: R vs S Carvone
R and S carvone are two stereoisomers of carvone, a p-menthane monoterpenoid found in many essential oils. The key difference between R and S carvone is their abundance and aroma:
Property | R-Carvone | S-Carvone |
---|---|---|
Abundance | Most abundant | Less abundant |
Aroma | Sweetish minty smell | Spicy aroma with a note of rye |
Both R and S carvone are used in various applications:
Application | R-Carvone | S-Carvone |
---|---|---|
Food flavoring | Yes | Yes |
Air freshening products | Yes | - |
Mosquito repellants | Yes | - |
Suppressant effect against a high-fat diet | - | Yes |
Prevention of premature sprouting of potatoes during storage | - | Yes |
Synthesizing terpenoid quassin | - | Yes |
R and S carvone have opposite configurations, with R carvone having a - Configuration and S carvone having a + Configuration. Chiral molecules like carvone are often labeled according to the sign of their specific rotation, as in (S)-(+)-carvone and (R)-(-)-carvone, or (±)-carvone for the racemic mixture.
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