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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. Ball-and-stick model - Wikipedia

    en.wikipedia.org/wiki/Ball-and-stick_model

    Double and triple bonds are usually represented by two or three curved rods, respectively, or alternately by correctly positioned sticks for the sigma and pi bonds. In a good model, the angles between the rods should be the same as the angles between the bonds , and the distances between the centers of the spheres should be proportional to the ...

  4. Trigonal planar molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Trigonal_planar_molecular...

    3), carbonate (CO 2− 3), and guanidinium (C(NH 2) + 3). In organic chemistry, planar, three-connected carbon centers that are trigonal planar are often described as having sp 2 hybridization. [2] [3] Nitrogen inversion is the distortion of pyramidal amines through a transition state that is trigonal planar.

  5. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    Two atomic orbitals in phase create a larger electron density, which leads to the σ orbital. If the two 1s orbitals are not in phase, a node between them causes a jump in energy, the σ* orbital. From the diagram you can deduce the bond order, how many bonds are formed between the two atoms. For this molecule it is equal to one.

  6. Triple bond - Wikipedia

    en.wikipedia.org/wiki/Triple_bond

    Triple bonding can be explained in terms of orbital hybridization. In the case of acetylene, each carbon atom has two sp-orbitals and two p-orbitals. The two sp-orbitals are linear, with 180° bond angles, and occupy the x-axis in the cartesian coordinate system. The p-orbitals are perpendicular to the sp-orbitals on the y-axis and the z-axis.

  7. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    For example, the C−H bond length is 110.2 pm in ethane, 108.5 pm in ethylene and 106.1 pm in acetylene, with carbon hybridizations sp 3 (25% s), sp 2 (33% s) and sp (50% s) respectively. To determine the degree of hybridization of each bond one can utilize a hybridization parameter (λ).

  8. Trigonal pyramidal molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Trigonal_pyramidal...

    3, and the sulfite ion, SO 2− 3. In organic chemistry, molecules which have a trigonal pyramidal geometry are sometimes described as sp 3 hybridized. The AXE method for VSEPR theory states that the classification is AX 3 E 1. Phosphine, an example of a molecule with a trigonal pyramidal geometry.

  9. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    The ammonia molecule (NH 3) has three pairs of electrons involved in bonding, but there is a lone pair of electrons on the nitrogen atom. [1]: 392–393 It is not bonded with another atom; however, it influences the overall shape through repulsions. As in methane above, there are four regions of electron density.