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  2. 2-Methylhexane - Wikipedia

    en.wikipedia.org/wiki/2-Methylhexane

    Compared to n-heptane, 2-methylhexane also has lower melting and boiling points. A lower density of liquid is found in 2-Methylhexane than heptane. On the NFPA 704 scale, 2-methylhexane is listed as a reactivity level-0 chemical, along with various other alkanes.

  3. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    3-Hydroxylcarbonyls, called aldols, release water upon standing at room temperature: RC(O)CH 2 CH(OH)R' → RC(O)CH=CHR' + H 2 O. The reaction is induced by dehydrating reagents. For example, 2-methyl-cyclohexan-1-ol dehydrates to 1-methylcyclohexene in the presence of Martin's sulfurane, which reacts irreversibly with water. [6] [7]

  4. Hexene - Wikipedia

    en.wikipedia.org/wiki/Hexene

    In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12. The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the " -ene " suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond .

  5. 2-Hexanone - Wikipedia

    en.wikipedia.org/wiki/2-hexanone

    2-Hexanone (methyl butyl ketone, MBK) is a ketone used as a general solvent and in paints. It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins. It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins.

  6. 1-Hexene - Wikipedia

    en.wikipedia.org/wiki/1-Hexene

    1-Hexene (hex-1-ene) is an organic compound with the formula C 6 H 12.It is an alkene that is classified in industry as higher olefin and an alpha-olefin, the latter term meaning that the double bond is located at the alpha (primary) position, endowing the compound with higher reactivity and thus useful chemical properties. 1-Hexene is an industrially significant linear alpha olefin.

  7. 1-Hexyne - Wikipedia

    en.wikipedia.org/wiki/1-Hexyne

    1-Hexyne can be prepared by the reaction of monosodium acetylide with butyl bromide: [1] NaC 2 H + BrC 4 H 9 → HC 2 C 4 H 9 + NaBr. Its reactivity illustrates the behavior of terminal alkylacetylenes. The hexyl derivative is common test substrate because it is conveniently volatile. It undergoes deprotonation at C-3 and C-1 with butyl lithium:

  8. MOSCED - Wikipedia

    en.wikipedia.org/wiki/MOSCED

    MOSCED (short for “modified separation of cohesive energy density" model) is a thermodynamic model for the estimation of limiting activity coefficients (also known as activity coefficient at infinite dilution).

  9. Hexyne - Wikipedia

    en.wikipedia.org/wiki/Hexyne

    The hexynes are a subgroup from the group of alkynes.It consists of several isomeric compounds having the formula C 6 H 10.. The linear and branched members are: 1-Hexyne (n-butylacetylene)