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When comparing a polar and nonpolar molecule with similar molar masses, the polar molecule in general has a higher boiling point, because the dipole–dipole interaction between polar molecules results in stronger intermolecular attractions. One common form of polar interaction is the hydrogen bond, which is also known as the H-bond.
Propylene glycol (IUPAC name: propane-1,2-diol) is a viscous, colorless liquid.It is almost odorless and has a faintly sweet taste. Its chemical formula is CH 3 CH(OH)CH 2 OH. . As it contains two alcohol groups, it is classified as a d
In chemistry, the carbon–hydrogen bond (C−H bond) is a chemical bond between carbon and hydrogen atoms that can be found in many organic compounds. [1] This bond is a covalent, single bond, meaning that carbon shares its outer valence electrons with up to four hydrogens. This completes both of their outer shells, making them stable. [2]
A pure substance is composed of only one type of isomer of a molecule (all have the same geometrical structure). Structural isomers have the same chemical formula but different physical arrangements, often forming alternate molecular geometries with very different properties. The atoms are not bonded (connected) together in the same orders.
Symmetry analysis using the Molecular Symmetry Group [4] [5] G 36 shows that one would need to analyse its high resolution rotation-vibration Raman spectrum to determine its equilibrium structure. 2-Butyne ( dimethylethyne ) forms with 5-decyne ( dibutylethyne ), 4-octyne ( dipropylethyne ) and 3-hexyne ( diethylethyne ) a group of symmetric ...
The chemical reaction called Sharpless asymmetric dihydroxylation can be used to produce chiral diols from alkenes using an osmate reagent and a chiral catalyst. Another method is the Woodward cis-hydroxylation (cis diol) and the related Prévost reaction (anti diol), which both use iodine and the silver salt of a carboxylic acid.
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CH 3 CH(OH)CH 2 CHO → CH 3 CH=CHCHO + H 2 O. Hydrogenation of 3-hydroxybutanal gives 1,3-butanediol: CH 3 CH(OH)CH 2 CHO + H 2 → CH 3 CH(OH)CH 2 CH 2 OH. This diol is a precursor to 1,3-butadiene, precursor to diverse polymers. Polymerization of 3-hydroxybutanal is also spontaneous, but can be stopped with the addition of water.