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  2. Methylpentene - Wikipedia

    en.wikipedia.org/wiki/Methylpentene

    Methylpentene is an alkene with a molecular formula C 6 H 12.The prefix "methyl-" is derived from the fact that there is a methyl(CH 3) branch, the word root "-pent-" is derived from the fact that there are 5 carbon atoms in the parent chain, while the "-ene" suffix denotes that there is a double bond present, as per IUPAC nomenclature. [1]

  3. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    The main use of ozonolysis is for the conversion of unsaturated fatty acids to value-added derivatives. Ozonolysis of oleic acid is an important route to azelaic acid. The coproduct is nonanoic acid: [20] CH 3 (CH 2) 7 CH=CH(CH 2) 7 CO 2 H} + 4 O 3 → HO 2 C(CH 2) 7 CO 2 H} + CH 3 (CH 2) 7 CO 2 H

  4. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    Pentenes are alkenes with the chemical formula C 5 H 10.Each molecule contains one double bond within its molecular structure. Six different compounds are in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure and whether the double bond has a cis or trans form.

  5. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    2 Na + 2 C 5 H 6 → 2 NaC 5 H 5 + H 2. Aromatization can entail removal of hydride. Tropylium, C 7 H + 7 arises by the aromatization reaction of cycloheptatriene with hydride acceptors. C 7 H 8 + Br 2 → C 7 H + 7 + Br − + HBr Ciamician-Dennstedt rearrangement of a pyrrole to a pyridine. The first step involves dearomatization. The second ...

  6. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  7. (2R)-2-Methylpent-4-enoic acid - Wikipedia

    en.wikipedia.org/wiki/(2R)-2-Methylpent-4-enoic_acid

    R)-2-Methylpent-4-enoic acid can also be used in synthesis of other chiral compounds. For example, it has been used in the process of synthesizing the drug Sacubitril as a reagent for adding a chiral center to the molecule. [2]

  8. Electrocyclic reaction - Wikipedia

    en.wikipedia.org/wiki/Electrocyclic_reaction

    The cis isomer exclusively yields cis,trans-hexa-2,4-diene whereas the trans isomer gives the trans,trans diene: [2] This reaction course can be explained in a simple analysis through the frontier-orbital method : the sigma bond in the reactant will open in such a way that the resulting p-orbitals will have the same symmetry as the HOMO of the ...

  9. 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.