12/9/17 química la química es la ciencia que estudia la materia, su composición, la organización de los elementos que la forman las transformaciones que. Isomería C8H FR. Felipe Rodriguez. Updated 14 November Transcript. Isómeros. C8H A continuación,. observarán.. La fórmula. -Isomería estructural- Ejemplo: La isomería estructural es importante dentro del estudio de la química orgánica ya que permite conocer la.

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The equatorial bonds are directed outward, toward the equator of the ring.

Estructura y Estereoquímica de Alcanos

For butane there will be two different staggered conformations: The methyl group is axial in one conformation, and equatorial in the other. The only intermolecular force of nonpolar molecules are London dispersion forces which quimicz from induced dipole attractions.

C5H12 C H 3 2 n-pentano iso-pentano neo-pentano Chapter 3.

Conformations of Cyclohexane Caption: Conformational Energy Diagram of Cyclohexane Caption: In the Newman projection it is easier to see the steric interaction between the methyl substituent and the hydrogens and carbons of the ring.

These conformations have equal energies, and they are present in equal amounts. Structures of some cycloalkanes. Cyclohexane can adopt four non-planar conformations: Two chair conformations are possible for cis-1,3-dimethylcyclohexane. Some common alkyl groups and their names.


The more stable conformation has both methyl groups in equatorial positions.

Isomeria estructural y geometrica. by Silvana Galicia on Prezi

All the C-H bonds are staggered in the chair conformation. To convert between these two conformations, the molecule must pass through the unstable half-chair conformation.

Because of their smaller surface areas, branched alkanes have lower boiling points organoca unbranched alkanes. The six-membered rings in cis- and trans-decalin assume chair conformations. To make this website work, we log user data and share it with processors.

The eclipsed conformation is about 3. The Newman Projection of Propane Caption: Conformations of Cyclobutane Caption: Conformational Analysis of Ethane Caption: The most stable conformation is the chair because it has all the C-H bonds staggered.

Propane is shown here as a perspective drawing and as a Newman projection looking down one of the carbon-carbon organjca. The chair conformation is most stable, followed by the twist boat. Much like ethane the staggered conformations of propane is lower in energy than the eclipsed conformations.

All the carbon-carbon bonds are eclipsed, generating torsional strain that contributes to the total ring strain. Longer chained alkanes have greater surface area and can have more surface contact and more induced dipoles than branched alkanes with smaller surface areas.

In the actual molecule, the boat conformation is skewed to give the twist boat, a conformation with less eclipsing of bonds and less interference between the two flagpole hydrogens. Either of the chair conformations of trans-1,3-dimethylcyclohexane has one methyl group in an axial position and one in an equatorial position. As they are numbered here, the odd-numbered carbons have their upward bonds axial and their downward bonds equatorial.


ORGÂNICA – Isomeria | Flashcards

Conformational Analysis of Propane Caption: Newman Projection of Methylcyclohexane: Numbering from left to right gives the first branch isimeria C2; numbering from right to left gives the first branch on C3, so we number from left to right. Folding gives partial relief from the eclipsing of bonds, as shown in the Newman projection.

The Newman projection is the best way to judge the stability of the different conformations of a molecule. Butano tiene 2 conformaciones alternadas diferentes: Sobre el proyecto SlidePlayer Condiciones de uso.

Often, the longest chain with the most substituents is not obvious.