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33 DIMETHYLPENTANE

  • Heptane
  • Chemical compound (C7H16)

    (chiral) 2,2-Dimethylpentane (neoheptane), H3C−C(CH3)2−CH2−CH2−CH3 2,3-Dimethylpentane, H3C−CH(CH3)−C*H(CH3)−CH2−CH3 (chiral) 2,4-Dimethylpentane,

    Heptane

    Heptane

    Heptane

  • 2,2-Dimethylbutane
  • Chemical compound

    Charles; McDougall, Gordon S. (1995). "Exchange reactions of 2,2-dimethylpentane, 2,2-dimethylbutane and 2,2-dimethylpropane over Pt/SiO2 and Rh/SiO2"

    2,2-Dimethylbutane

    2,2-Dimethylbutane

    2,2-Dimethylbutane

  • Brown-banded cockroach
  • Species of cockroach

    lipase-catalyzed desymmetrization or enantiomer separation of syn- or anti-2,4-dimethylpentane-1,5-diol. Supellapyrone has four configurations but female brown-banded

    Brown-banded cockroach

    Brown-banded cockroach

    Brown-banded_cockroach

  • Alkane
  • Type of saturated hydrocarbon compound

    (isoheptane), 3-methylhexane, 2,2-dimethylpentane (neoheptane), 2,3-dimethylpentane, 2,4-dimethylpentane, 3,3-dimethylpentane, 3-ethylpentane, 2,2,3-trimethylbutane

    Alkane

    Alkane

    Alkane

  • Heat of combustion
  • Amount of heat released by combustion of a quantity of substance

    which treats carbon, hydrogen, sulfur as combustible elements: HHV [kJ/g] = 33.87 mC + 122.3 (mH − mO/8) + 9.4 mS where mC, mH, mO and mS are the mass fractions

    Heat of combustion

    Heat_of_combustion

  • Standard enthalpy of formation
  • Change of enthalpy during the formation of a compound from its elements

    C7H16 2,2-Dimethylpentane −49.2 −205.9 C7H16 2,2,3-Trimethylbutane −49.0 −205.0 C7H16 3,3-Dimethylpentane −48.1 −201.3 C7H16 2,3-Dimethylpentane −47.3 −197

    Standard enthalpy of formation

    Standard_enthalpy_of_formation

  • IUPAC nomenclature of organic chemistry
  • System for naming organic chemical compounds

    purpose of alphabetical ordering of side chains (e.g. 3-ethyl-2,4-dimethylpentane, not 2,4-dimethyl-3-ethylpentane). Alkenes are named for their parent

    IUPAC nomenclature of organic chemistry

    IUPAC_nomenclature_of_organic_chemistry

  • Asymmetric hydrogenation
  • Chemical reaction

    PMID 19719102. Zhou, J.; Burgess, K. (2007). "Α,ω-Functionalized 2,4-Dimethylpentane Dyads and 2,4,6-Trimethylheptane Triads through Asymmetric Hydrogenation"

    Asymmetric hydrogenation

    Asymmetric_hydrogenation

  • MOSCED
  • Thermodynamic model for the estimation of limiting activity coefficients

    1.00 2.40 2.08 2,2-dimethylpentane 148.9 14.26 0.00 1.00 0.00 0.00 iodoethane 93.6 17.39 3.58 1.00 0.51 1.96 2,4-dimethylpentane 150.0 14.29 0.00 1.00

    MOSCED

    MOSCED

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