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  2. IUPAC nomenclature of organic chemistry - Wikipedia

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

    If the carbon in the carbonyl group cannot be included in the attached chain (for instance in the case of cyclic aldehydes), the prefix "formyl-" or the suffix "-carbaldehyde" is used: C 6 H 11 CHO is cyclohexanecarbaldehyde. If an aldehyde is attached to a benzene and is the main functional group, the suffix becomes benzaldehyde.

  3. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [ 1 ] [ 2 ] Number of C atoms

  4. -ol - Wikipedia

    en.wikipedia.org/wiki/-ol

    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. Use standard Greek prefixes to name molecules with two or more -OH groups (di- for 2, and so on). [1]

  5. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    From Figure 1, oxy subunits are take precedence over acyclic carbon chain subunits. The preferred CRU is chosen as that with the lowest possible locant (s) for substituents . In the example, there is a bromo-substituted -CH 2 -CH 2 - subunit. 1-Bromoethane-1,2-diyl is chosen in preference to 2- bromoethane-1,2-diyl as the former has a lower ...

  6. IUPAC nomenclature of chemistry - Wikipedia

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

    For example, one can deduce that 1-chloropropane has a Chlorine atom on the first carbon in the 3-carbon propane chain. History "Well being" of standardizing science ...

  7. Substituent - Wikipedia

    en.wikipedia.org/wiki/Substituent

    The more general method omits only the terminal "e" of the substituent name, but requires explicit numbering of each yl prefix, even at position 1 (except for -ylidyne, which as a triple bond must terminate the substituent carbon chain). Pentan-1-yl is an example of a name by this method, and is synonymous with pentyl from the previous guideline.

  8. Locant - Wikipedia

    en.wikipedia.org/wiki/Locant

    The α-carbon (alpha-carbon) refers to the first carbon atom that attaches to a functional group, such as a carbonyl. The second carbon atom is called the β-carbon ( beta -carbon), the third is the γ-carbon ( gamma -carbon), and the naming system continues in alphabetical order.

  9. Alk- - Wikipedia

    en.wikipedia.org/wiki/Alk-

    Some examples include: meth- (1 carbon) eth- (2 carbons) prop- (3 carbons) but- (4 carbons) pent- (5 carbons) hex- (6 carbons) Alkyl group prefixes: These prefixes are used to name alkyl groups (chains of carbon atoms) that are attached to another molecule. They are formed by adding the suffix "-yl" to the hydrocarbon prefix.