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Solvent bonding differs from adhesive bonding, because the solvent does not become a permanent addition to the joined substrate. [4] Solvent bonding differs from other plastic welding processes in that heating energy is generated by the chemical reaction between the solvent and thermoplastic, and cooling occurs during evaporation of the solvent ...
Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5] Cyclohexyl (C 6 H 11) is the alkyl substituent of cyclohexane and is ...
log 10 of Cyclohexane vapor pressure. Uses formula: log e P m m H g = {\displaystyle \scriptstyle \log _{e}P_{mmHg}=} log e ( 760 101.325 ) − 9.200978 log e ( T + 273.15 ) − 6354.898 T + 273.15 + 75.65058 + 7.374814 × 10 − 06 ( T + 273.15 ) 2 {\displaystyle \scriptstyle \log _{e}({\frac {760}{101.325}})-9.200978\log _{e}(T+ ...
Cyclohexane is the most stable of the cycloalkanes, due to the stability of adapting to its chair conformer. [4] This conformer stability allows cyclohexane to be used as a standard in lab analyses. More specifically, cyclohexane is used as a standard for pharmaceutical reference in solvent analysis of pharmaceutical compounds and raw materials.
For example, if induced dipole was a controlling effect, aliphatic compounds such as cyclohexane should be good cation–π partners (but are not). [4] The cation–π interaction is noncovalent and is therefore fundamentally different than bonding between transition metals and π systems.
The intramolecular H-bond formed in the cis-enol form is more pronounced when there is no competition for intermolecular H-bonding with the solvent. As a result, solvents of low polarity that do not readily participate in H-bonding allow cis -enolic stabilization by intramolecular H-bonding.
Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.
Examples include a molecule with a carbon–carbon double bond (an alkene) or a triple bond (an alkyne). Another example is a compound that has rings (which are also considered points of unsaturation). A molecule that has carbon—heteroatom double bonds, such as a carbonyl group (C=O) or imine group (C=N), can undergo an addition reaction ...