Hydrophilic: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>David E. Volk
imported>David E. Volk
No edit summary
Line 13: Line 13:
== Cells ==
== Cells ==
All biological [[cell]]s maintence micelle bilayers that separate the cell from the outside world.  These bilayers are formed when when the hydrophilic ends of long fatty acids are attacked to each other, leaving the hydrophobic ends displayed to the outside world.  Polar chemicals then need to be escorted into and out of the cell by transporter proteins or specialized pores to get through this hydrophobic region.
All biological [[cell]]s maintence micelle bilayers that separate the cell from the outside world.  These bilayers are formed when when the hydrophilic ends of long fatty acids are attacked to each other, leaving the hydrophobic ends displayed to the outside world.  Polar chemicals then need to be escorted into and out of the cell by transporter proteins or specialized pores to get through this hydrophobic region.
== References ==
<references/>

Revision as of 09:42, 2 April 2008

This article is a stub and thus not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and subject to a disclaimer.

Hydrophilic is a chemical term indicating that a chemical compound or group is water loving. Its opposite is the term hydrophobic, meaning water-repelling or water-fearing. Hydrophilic and hydrophobic properties of chemicals play a significant role in chemical reactions, detergents and more importantly in the organization living organisms. Hydrophilic parts of chemicals often carry an electric charge or they are polar, and they are attracked to each other by charge-charge are dipole-dipole interactions. Hydrophobic parts of molecules are usually alkanes or aromatic in nature, and they are attracked to each other mostly by van der Waals forces.

Solubility

The relative hydrophilicity or hydrophicity of chemical compounds plays are large role in determining which solvents a particular chemical will be soluble in, and thus determines the conditions needed to perform a chemical reaction. A reaction between two hydrophilic compounds is very unlikely to occur in benzene, for example, because it is very hydrophobic.

Soaps

Sodium lauryl sulfate (sodium dodecanyl sulfate), a typical detergent molecule

Soaps and detergents[1] owe their action to a combination of hydrophilic and hydrophobic ends on the same molecule. The hydrophic ends are attracked to each other, and grease, for example, by hydrophobic interactions. The hydrophilic ends of soap molecules are attracked to water. The result is that the hydrophobic aliphatic ends of the soap molecules surround the dirt or grease, with the hydrophilic ends pointing outwards, thus making the grease removable as a spherical micelle. The grease is said to be emulsified, that is, held in solution in a solvent in which it is not normally soluble.

Cells

All biological cells maintence micelle bilayers that separate the cell from the outside world. These bilayers are formed when when the hydrophilic ends of long fatty acids are attacked to each other, leaving the hydrophobic ends displayed to the outside world. Polar chemicals then need to be escorted into and out of the cell by transporter proteins or specialized pores to get through this hydrophobic region.

References

  1. Soaps are sodium salts of fatty acids, which tend to precipitate in hard water containing magnesium or calcium ions, leaving a scum. Detergents contain other hydrophlic groups, like sulfate, to reduce scum buildup.