Isomeria Conformacional. fhmateo; 3 videos; 18 views; Last updated on Oct 11, Play all. Share. Loading Save. Empleo de la notación E-Z en la isomería Cis-Trans | | UPV – Duration: Universitat. Isomería de conformacional de alcanos y ciclo alcanos. Isomería conformacional (cis-trans): en dobles enlaces, en anillo.

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Pure conformers cannot be isolated in most cases, because the molecules are constantly rotating through all the possible conformations.

Butano tiene 2 conformaciones alternadas diferentes: Some groups are isometia bulky that they are extremely hindered in axial positions. The eclipsed conformation is about 3. Angle strain and torsional strain account for the high reactivity of 4-membered rings.

This puckered conformation reduces the eclipsing of adjacent CH2 groups. Los botones se encuentran debajo. Numbering from left to right gives the first branch on C2; numbering from right to left gives the first branch on C3, so we number from confprmacional to right. The angle compression for butane is Conformations of Cyclohexane Caption: Chair Conformation of Cyclohexane Caption: Alkanes with an even number of carbons pack better than those with an odd number of carbons.

Methane is perfectly tetrahedral, with the C5H12 C H 3 2 n-pentano iso-pentano neo-pentano Chapter 3. The six-membered rings in cis- and trans-decalin assume chair conformations.

Rotations about the center bond in butane give different molecular shapes. The conformation of cyclopentane is slightly folded, like the shape of an envelope.


This interference is called a 1,3-diaxial interaction. The angle compression of cyclopropane is Regardless of the other groups present, the most stable conformation has a t-butyl group in an equatorial position.

Conformations of Cyclopropane Caption: Same Length Chains Caption: In the symmetrical boat conformation of cyclohexane, eclipsing of bonds results in torsional strain.

The more stable conformation has both methyl groups in equatorial positions. The even-numbered carbons have their downward bonds axial and their upward bonds equatorial. Chair Conformations of cis-1,3-Dimethylcyclohexane Caption: Longer chained alkanes have greater surface area and coformacional have more surface contact and more induced concormacional than branched alkanes with smaller surface areas. Chair Conformations of trans-1,3-Dimethylcyclohexane Caption: The equatorial bonds are directed outward, toward the equator of the ring.

The unfavorable conformation has both methyl groups in axial positions, with a 1,3-diaxial interaction between them.

At room temperature, this barrier is easily overcome, and the molecules rotate constantly. Newman Projections of Butane Caption: The high reactivity of cyclopropanes is due to the non-linear overlap of the sp3 orbitals.

The most stable conformation is the chair conformacinal it has all the C-H bonds staggered. Three of these conformations are given specific names.

Isomería – Wikipedia

La eclipsada es 3. The following figure shows the severe steric interactions in a chair conformation with a t-butyl group axial. Chair-chair interconversion of methylcyclohexane.

Since the methyl group occupies more space than a hydrogen, the torsional strain will be 0.

Isomerisme conformacional

The totally eclipsed conformation is about 1. Melting Points of Alkanes Caption: The angle strain and the torsional strain in cyclopropane make this ring size extremely reactive. The Newman projection is the best way to judge the stability of the different conformations of a molecule. The torsional energy of ethane is lowest in the staggered conformation.


Some common alkyl groups and their names. The anti conformation is lowest in energy, and the totally eclipsed conformation is highest in energy.

Propane conformaciona shown here as a perspective drawing and as a Newman isomeriw looking down one of the carbon-carbon bonds. Isojeria interferencia es llamada interacciones 1,3-diaxial. The melting point curve for n-alkanes with even numbers of carbon atoms is slightly higher than that for alkanes with odd numbers of carbons.

Because of their smaller surface areas, branched alkanes have lower boiling points than unbranched alkanes. Compare this actual structure with the hypothetical planar structure in Figure The four hydrogen atoms are covalently bonded to the central carbon atom, with bond lengths of 1. Ethane, the two-carbon comformacional, is composed of two methyl groups with overlapping sp3 hybrid orbitals forming a sigma bond between them. Cyclohexane can adopt four non-planar conformations: