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Camphor can also be synthetically produced from oil of turpentine. The compound is chiral, existing in two possible enantiomers as shown in the structural diagrams. The structure on the left is the naturally occurring (+)-camphor ((1R,4R)-bornan-2-one), while its mirror image shown on the right is the (−)-camphor ((1S,4S)-bornan-2-one ...
Camphorsulfonic acid, sometimes abbreviated CSA or 10-CSA is an organosulfur compound.Like typical sulfonic acids, it is a relatively strong acid that is a colorless solid at room temperature and is soluble in water and a wide variety of organic substances.
Camphoric acid, C 10 H 16 O 4 [citation needed] or in Latin form Acidum camphoricum, is a white crystallisable substance obtained from the oxidation of camphor. It exists in three optically different forms; the dextrorotatory one is obtained by the oxidation of dextrorotatory camphor and is used in pharmaceuticals .
Cyclohexanol is the organic compound with the formula HOCH(CH 2) 5.The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group. [4] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature.
tert-Butyl alcohol is the simplest tertiary alcohol, with a formula of (CH 3) 3 COH (sometimes represented as t-BuOH). Its isomers are 1-butanol, isobutanol, and butan-2-ol. tert-Butyl alcohol is a colorless solid, which melts near room temperature and has a camphor-like odor. It is miscible with water, ethanol and diethyl ether.
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Julius Bredt (29 March 1855 – 21 September 1937) was a German organic chemist. He was the first to determine, in 1893, the correct structure of camphor.Bredt also proposed in 1924 that a double bond cannot be placed at the bridgehead of a bridged ring system, a statement now known as Bredt's rule. [1]
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