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  2. Linear molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Linear_molecular_geometry

    Linear organic molecules, such as acetylene (HC≡CH), are often described by invoking sp orbital hybridization for their carbon centers. Two sp orbitals. According to the VSEPR model (Valence Shell Electron Pair Repulsion model), linear geometry occurs at central atoms with two bonded atoms and zero or three lone pairs (AX 2 or AX 2 E 3) in ...

  3. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    A polar molecule has a net dipole as a result of the opposing charges (i.e. having partial positive and partial negative charges) from polar bonds arranged asymmetrically. Water (H 2 O) is an example of a polar molecule since it has a slight positive charge on one side and a slight negative charge on the other. The dipoles do not cancel out ...

  4. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    Linear: In a linear model, atoms are connected in a straight line. The bond angles are set at 180°. For example, carbon dioxide and nitric oxide have a linear molecular shape. Trigonal planar: Molecules with the trigonal planar shape are somewhat triangular and in one plane (flat). Consequently, the bond angles are set at 120°.

  5. Intermolecular force - Wikipedia

    en.wikipedia.org/wiki/Intermolecular_force

    The polar water molecules surround themselves around ions in water and the energy released during the process is known as hydration enthalpy. The interaction has its immense importance in justifying the stability of various ions (like Cu 2+) in water. An ion–induced dipole force consists of an ion and a non-polar molecule interacting.

  6. Molecular graph - Wikipedia

    en.wikipedia.org/wiki/Molecular_graph

    In chemical graph theory and in mathematical chemistry, a molecular graph or chemical graph is a representation of the structural formula of a chemical compound in terms of graph theory. A chemical graph is a labeled graph whose vertices correspond to the atoms of the compound and edges correspond to chemical bonds.

  7. Optical rotation - Wikipedia

    en.wikipedia.org/wiki/Optical_rotation

    The "D-" and "L-" prefixes are used to specify the enantiomer of chiral organic compounds in biochemistry and are based on the compound's absolute configuration relative to (+)-glyceraldehyde, which is the D-form by definition. The prefix used to indicate absolute configuration is not directly related to the (+) or (−) prefix used to indicate ...

  8. Dicarbon monoxide - Wikipedia

    en.wikipedia.org/wiki/Dicarbon_monoxide

    Dicarbon monoxide is a product of the photolysis of carbon suboxide: [2] [3]. C 3 O 2 → CO + C 2 O. It is stable enough to observe reactions with NO and NO 2. [4]Called ketenylidene in organometallic chemistry, it is a ligand observed in metal carbonyl clusters, e.g. [OC 2 Co 3 (CO) 9] +.

  9. Partition coefficient - Wikipedia

    en.wikipedia.org/wiki/Partition_coefficient

    The hydrophobicity of a compound can give scientists an indication of how easily a compound might be taken up in groundwater to pollute waterways, and its toxicity to animals and aquatic life. [34] Partition coefficient can also be used to predict the mobility of radionuclides in groundwater. [ 35 ]