Why is a molecule of #CH_4# nonpolar?
The dipoles cancel out each other, depicted in a VSEPR diagram.
When determining the polarity of a molecule, we use 2 methods:
#1: Electrongativity,
#2: Symmetry of molecule.
- Electronegativity:
Electronegativity of a compound can be calculated by subtracting the element with the highest electronegativity with the lowest. Electronegativity can be found on the periodic table:
Compounds with an electronegativity of
#0.0->0.6# are non-polar molecules.#0.7->1.7# are polar molecules, and#1.7+# are ionic compounds.In methane's case,
#2.5-2.1=0.4# Disclaimer: electronegativity only determines the intramolecular bond within a compound. Not the overall compound's polarity. To do this, we use symmetry.
- Molecular Symmetry:
Molecular symmetry is the use of geometrical arrangement that can help predict the shape of molecules. These arrangements are called VSEPR: Valence Shell Electron Pair Repulsion. Lewis diagrams work too, but lacks additional/specific information that is necessary for a more "academic" standard, that a VSEPR diagram provides.
When a molecule is "symmetrical", it means the dipoles cancel. This only occurs when the outside atoms are arranged in such a way that surrounds the central atom, where the dipoles cancel - no side of the molecule has more charge (positive or negative} than the other(s).
In methane's case,
All the outer atoms are the same - the same dipoles, and that the dipole moments are in the same direction - towards the carbon atom, the overall molecule becomes non-polar.
Therefore, methane has non-polar bonds, and is non-polar overall.
Keep in mind that molecules can have polar bonds, but be non-polar overall.
Hope this helps :)
- Molecular Symmetry:
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A molecule of CH₄ (methane) is nonpolar because it has a symmetrical tetrahedral shape with identical hydrogen atoms surrounding the central carbon atom. The electronegativity difference between carbon and hydrogen is relatively small, resulting in equally distributed electron density, leading to a nonpolar molecule.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
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