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  2. Isopropyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_alcohol

    Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol) is a colorless, flammable, organic compound with a pungent alcoholic odor. [9]Isopropyl alcohol, an organic polar molecule, is miscible in water, ethanol, and chloroform, demonstrating its ability to dissolve a wide range of substances including ethyl cellulose, polyvinyl butyral, oils, alkaloids, and natural ...

  3. Propanol - Wikipedia

    en.wikipedia.org/wiki/Propanol

    Propanal (propionaldehyde) differs in spelling from propanol by a single letter and is a different compound. Propranolol is a drug used for reducing blood pressure and hand tremors. Index of chemical compounds with the same name

  4. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    In traditional names various qualifiers are used to label isomers, for example, isopropanol (IUPAC name: propan-2-ol) is an isomer of n-propanol (propan-1-ol). The term moiety has some overlap with the term "functional group". However, a moiety is an entire "half" of a molecule, which can be not only a single functional group, but also a larger ...

  5. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...

  6. Hexafluoro-2-propanol - Wikipedia

    en.wikipedia.org/wiki/Hexafluoro-2-propanol

    It is also relatively acidic, with a pKa of 9.3, comparable to that for phenol. [1] It is classified as a hard Lewis acid and its acceptor properties are discussed in the ECW model. [3] [4] Hexafluoro-propan-2-ol is a speciality solvent for organic synthesis, particularly for

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Alcohols (R−OH) take the suffix "-ol" with a numerical suffix indicating the bonding position: CH 3 CH 2 CH 2 OH is propan-1-ol. The suffixes -diol, -triol, -tetrol, etc., are used for multiple −OH groups: Ethylene glycol CH 2 OHCH 2 OH is ethane-1,2-diol.

  8. C3H6O - Wikipedia

    en.wikipedia.org/wiki/C3H6O

    The molecular formula C 3 H 6 O may refer to: . Chemistry portal; Alcohols. Allyl alcohol or 2-propen-1-ol, CH 2 =CH-CH 2 OH, CAS number 107-18-6; cyclopropanol or cyclopropyl alcohol, cyclo (-CH 2-CH 2-HOHC-), CAS number 16545-68-9

  9. -ol - Wikipedia

    en.wikipedia.org/wiki/-ol

    To be alcohol, the -OH must be bonded to a carbon. Use the suffix -ol to denote which carbon the alcohol group is on. A three-carbon chain with the -OH on the second carbon would be propan-2-ol. Note that in some instances, common names are better. If the -OH is on the end of the chain, or the carbon chain is only 1 or 2, use no number.