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  2. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    This hydrocarbon group occurs in many organic compounds. It is a very stable group in most molecules. It is a very stable group in most molecules. While the methyl group is usually part of a larger molecule , bonded to the rest of the molecule by a single covalent bond ( −CH 3 ), it can be found on its own in any of three forms: methanide ...

  3. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    Nonpolar bonds generally occur when the difference in electronegativity between the two atoms is less than 0.5; Polar bonds generally occur when the difference in electronegativity between the two atoms is roughly between 0.5 and 2.0; Ionic bonds generally occur when the difference in electronegativity between the two atoms is greater than 2.0

  4. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    The tetrahedral molecule methane (CH 4)Aside from virtually all saturated organic compounds, most compounds of Si, Ge, and Sn are tetrahedral. Often tetrahedral molecules feature multiple bonding to the outer ligands, as in xenon tetroxide (XeO 4), the perchlorate ion (ClO − 4), the sulfate ion (SO 2− 4), the phosphate ion (PO 3− 4).

  5. Non-covalent interaction - Wikipedia

    en.wikipedia.org/wiki/Non-covalent_interaction

    Non-covalent metallo drugs have been developed. For example, dinuclear triple-helical compounds in which three ligand strands wrap around two metals, resulting in a roughly cylindrical tetracation have been prepared. These compounds bind to the less-common nucleic acid structures, such as duplex DNA, Y-shaped fork structures and 4-way junctions ...

  6. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    Most compounds considered to be Lewis acids require an activation step prior to formation of the adduct with the Lewis base. Complex compounds such as Et 3 Al 2 Cl 3 and AlCl 3 are treated as trigonal planar Lewis acids but exist as aggregates and polymers that must be degraded by the Lewis base. [10] A simpler case is the formation of adducts ...

  7. Methyl radical - Wikipedia

    en.wikipedia.org/wiki/Methyl_radical

    The carbon centre in methyl can bond with electron-donating molecules by reacting: CH • 3 + R • → RCH 3. Because of the capture of the nucleophile (R •), methyl has oxidising character. Methyl is a strong oxidant with organic chemicals. However, it is equally a strong reductant with chemicals such as water.

  8. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    The carbonyl center of an acyl radical has one non-bonded electron with which it forms a chemical bond to the remainder (denoted with the letter R) of the molecule. The acetyl moiety is a component of many organic compounds , including acetic acid , the neurotransmitter acetylcholine , acetyl-CoA , acetylcysteine , acetaminophen (also known as ...

  9. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    It refers to the hydrogen atoms not attached to atoms with double bonds in the ring system. Has the lowest-numbered locants for the suffix functional group. Has the lowest-numbered locants for multiple bonds ('ene', 'yne'), and hydro prefixes. (The locant of a multiple bond is the number of the adjacent carbon with a lower number).