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|Section2= |Section3= |Section8= }} Borneol is a bicyclic organic compound and a terpene. The hydroxyl group in this compound is placed in an ''endo'' position. There are two different enantiomers of borneol. Both ''d''-(+)-borneol and ''l''-(–)-borneol are found in nature. ==Reactions == Borneol is easily oxidized to the ketone (camphor). One historical name for borneol is Borneo camphor which explains the name. Borneol can be synthesized by reduction of camphor by the Meerwein–Ponndorf–Verley reduction (a reversible process). Reduction of camphor with sodium borohydride (fast and irreversible) gives instead the isomer isoborneol as the kinetically controlled reaction product. : 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Borneol」の詳細全文を読む スポンサード リンク
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