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  2. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    3D structure A Newman projection is a drawing that helps visualize the 3-dimensional structure of a molecule. [ 1 ] This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes.

  3. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Thus, the name is 3-methylpentane to avoid ambiguity: The 3- is because the methyl is attached to the third of the five carbon atoms. If there is more than one of the same alkyl group attached to a chain, then the prefixes are used on the alkyl groups to indicate multiples (i.e., di, tri, tetra, etc.)

  4. 3-Methylpentane - Wikipedia

    en.wikipedia.org/wiki/3-Methylpentane

    3-Methylpentane is a branched alkane with the molecular formula C 6 H 14. It is a structural isomer of hexane composed of a methyl group bonded to the third carbon atom in a pentane chain. It is of similar structure to the isomeric 2-methylpentane , which has the methyl group located on the second carbon of the pentane chain.

  5. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    Alkanes with more than three carbon atoms can be arranged in various ways, forming structural isomers.The simplest isomer of an alkane is the one in which the carbon atoms are arranged in a single chain with no branches.

  6. 2-Methylpentane - Wikipedia

    en.wikipedia.org/wiki/2-Methylpentane

    2-Methylpentane, trivially known as isohexane, is a branched-chain alkane with the molecular formula C 6 H 14. It is a structural isomer of hexane composed of a methyl group bonded to the second carbon atom in a pentane chain.

  7. C6H14 - Wikipedia

    en.wikipedia.org/wiki/C6H14

    3-Methylpentane Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  8. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one ...

  9. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    ch 2 =ch 2 + ch 3 ch=chch 32 ch 2 =chch 3 Transition metal catalyzed hydrovinylation is another important alkene synthesis process starting from alkene itself. [ 31 ] It involves the addition of a hydrogen and a vinyl group (or an alkenyl group) across a double bond.