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  2. List of isomers of dodecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_dodecane

    The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.

  3. List of isomers of decane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_decane

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  4. List of isomers of tetradecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_tetradecane

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  5. 2,2,4-Trimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,2,4-Trimethylpentane

    2,2,4-Trimethylpentane, also known as isooctane or iso-octane, is an organic compound with the formula (CH 3) 3 CCH 2 CH(CH 3) 2. It is one of several isomers of octane (C 8 H 18 ). This particular isomer is the standard 100 point on the octane rating scale (the zero point is n -heptane ).

  6. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    The Ph 3 C-H bond is relatively weak, with a bond dissociation energy (BDE) of 81 kcal/mol, or about 24 kcal/mol less than methane. [4] Correspondingly, triphenylmethane is mildly acidic, with a pK a of 33.297. [5] Triphenylmethane is significantly more acidic than most other hydrocarbons because the charge is delocalized over three phenyl ...

  7. Triptane - Wikipedia

    en.wikipedia.org/wiki/Triptane

    Triptane, or 2,2,3-trimethylbutane, is an organic chemical compound with the molecular formula C 7 H 16 or (H 3 C-) 3 C-C(-CH 3) 2 H. It is therefore an alkane, specifically the most compact and heavily branched of the heptane isomers, the only one with a butane (C 4) backbone.

  8. List of isomers of nonane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_nonane

    5.2 Dimethyl+ethyl. 5.3 Diethyl. Toggle the table of contents. List of isomers of nonane. 4 languages.

  9. IUPAC nomenclature of organic chemistry - Wikipedia

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

    The side chains are: an ethyl- at carbon 4, an ethyl- at carbon 8, and a butyl- at carbon 12. Note: the −O−CH 3 at carbon atom 15 is not a side chain, but it is a methoxy functional group. There are two ethyl- groups. They are combined to create, 4,8-diethyl. The side chains are grouped like this: 12-butyl-4,8-diethyl.