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Encyclopedia > Molecular structure
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Geometry of the water molecule

Molecules have fixed equilibrium geometries--bond lengths and angles--that are dictated by the laws of quantum mechanics. The chemical formula and the structure of a molecule are the two most important factors that determine its properties, particularly its reactivity. Molecules are most often held together with covalent bonds involving single, double, and/or triple bonds (shared electron pairs).


A pure substance is composed of molecules with the same geometrical structure. Isomers share a chemical formula but have different geometries, resulting in very different properties. Stereoisomers, a particular type of isomers, may have very similar physico-chemical properties and at the same time very different biochemical activities.


Protein folding refers to the complex geometries and different isomers that proteins can take.

Contents

Hybridization of Orbitals

Bonds in molecules are often the result of hybridization, for two main reasons. First, sometimes electrons from two different orbital types are paired together. A middle ground is needed where both of the electrons can exist with some aspects of their native orbital. Second, sigma bonds are closer to the respective nuclei and thus take less energy to form and maintain. Since reactions tend to occur using the least amount of energy possible, sigma bonds are the most common type of hybrid bond.


Sigma Bonds

Sigma Bonds are those bonds between atoms in a molecule that exhibit hybridization. Sigma bonds are named after the Greek letter "σ", as in s orbitals. Sigma bonds require that both atoms give an electron from the s orbital in conjunction with additional electrons from the p and sometimes d (and above) orbitals. Sigma bonds are the strongest type of covalent bonds. They result in a head-to-head orbital overlap - the two combined orbitals meet at the more narrow points. Electrons in sigma bonds are sometimes referred to as sigma electrons.


Pi Bonds

Pi bonds are those bonds between two atoms in a molecule that do not exhibit hybridization. Pi bonds are named after the Greek letter "π", as in p orbitals. Pi bonds are direct sharing of electrons between two atoms' p orbitals. Pi bonds are weaker than sigma bonds because their orbitals go further from the positive charge of the nucleus, which requires more energy. As a result, sigma bonds are naturally preferred over pi bonds. However, there is a limit of one sigma bond for each pair of atoms. Atoms with double or triple bonds have one sigma bond and the rest are usually pi bonds. Pi bonds result from parallel orbital overlap - the two combined orbitals meet lengthwise and create longer bonds than the sigma bonds. Electrons in Pi Bonds are sometimes referred to as pi electrons.


VSEPR Model

The VSEPR (Valence-Shell Electron-Pair Repulsion) model is one way to generally represent the geometric shape individual molecules will take. It is not perfectly accurate but instead gives a general impression of how atoms and electrons will be arranged. The AXE method is commonly used in formatting molecules to fit the VSEPR model. The A represents the central atom and is always (implied) subscript one. The X represents how many bonds are formed between the central atoms and outside atoms. Multiple covalent bonds (double, triple, etc) count as one X. The E represents the number of lone electron pairs present outside of the central atom. Once the AXE formula has been found, the following table will predict the geometric configuration around the central atom.

Molecular Geometries
Type Shape
AX2E0 Linear
AX2E1 Bent
AX2E2 Bent
AX2E3 Linear
AX3E0 Trigonal Planar
AX3E1 Trigonal Pyramidal
AX3E2 T-shaped
AX4E0 Tetrahedral
AX4E1 Seesaw
AX4E2 Square Planar
AX5E0 Triangular Bipyramidal
AX5E1 Square Pyramidal
AX6E0 Octahedral

See also

atomic orbital, molecular orbital, electron configuration, covalent bond, valence bond theory


  Results from FactBites:
 
Molecular Structure - The rise and reemergence of atomism (1802 words)
Distinct molecular structural units that have the same connectivities but varying three-dimensional arrangements are also isomers.
Particle-based models for atomic and molecular structure soon gave way to the quantum mechanical view, in which electrons are not treated as localized, discrete particles (electrons orbiting around a nucleus), but as delocalized areas of wavelike charge, each possessing a given probability of being found in a given location near an atomic nucleus (an orbital).
Molecular orbitals describe three-dimensional arrangements of the atomic nuclei in a molecule and the probability that any given electron of a given energy will occupy a given location with respect to those nuclei.
Molecular Structure & Bonding (3607 words)
In the formula on the right all four 1º-carbons are structurally equivalent (remember the tetrahedral configuration of tetravalent carbon); however the central formula has two equivalent 1º-carbons (bonded to the 3º carbon on the left end) and a single, structurally different 1º-carbon (bonded to the 2º-carbon) at the right end.
Although structural formulas are essential to the unique description of organic compounds, it is interesting and instructive to evaluate the information that may be obtained from a molecular formula alone.
The double bonded structure is regarded as the major contributor, the middle structure a minor contributor and the right hand structure a non-contributor.
  More results at FactBites »


 

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