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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Conformations with Extremely Bulky Groups Caption: The equatorial bonds are directed outward, toward the equator of the ring.

Isomerisme conformacional

All the C-H bonds are staggered in the chair conformation. Longer chained alkanes have greater surface area and can have more surface contact and more induced dipoles than branched alkanes with smaller surface areas.

The Newman Projection of Propane Caption: Torsional energy of butane. Viewed from the Newman projection, the chair conformation has no eclipsing of the carbon-carbon bonds. Melting Points of Alkanes Caption: The different arrangement formed by rotations about a single bond are called conformations, and a specific is called conformer.

The molecular formula of alkanes is CnH2n, two hydrogen less confkrmacional an open chain alkane. When looking for the longest continuous chain, look to find all the different chains of that length.

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Cyclohexane can adopt four non-planar conformations: Angle strain in cyclopropane. The following figure shows the severe steric interactions in a chair conformation with a conforkacional group axial.


Three of these conformations are given specific names. Rotations about the center bond in butane give different molecular shapes.

Often, the longest chain with the most substituents is not obvious. Conformations of Cyclopentane Caption: 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. Newman Projection of Methylcyclohexane: Cyclobutane adopts the folded conformation to decrease the torsional strain caused by eclipsing hydrogens.

Axial hydrogens are pointed straight up or down, parallel to the axis isomeriia the ring. As they are numbered here, the odd-numbered carbons have their upward bonds axial and their downward bonds equatorial. Alcanos con par de C tienen p.

Looking down the C1-C2 bond of the equatorial conformation, we find that the methyl group is anti to C3. Esta interferencia es llamada interacciones 1,3-diaxial. Because of their smaller surface areas, branched alkanes have lower boiling points than unbranched alkanes. Chair Conformations of trans-1,3-Dimethylcyclohexane Caption: Torsional strain in cyclopropane. Two chair conformations are possible for cis-1,3-dimethylcyclohexane.

Solution The longest carbon chain contains eight carbon atoms, so this compound is named as an octane. Folding gives partial relief from the eclipsing of bonds, as shown in the Newman projection. For butane there will be two different staggered conformations: When molecules can pack in neat order avoiding empty pockets the melting point will be higher than when the packing is not ordered.


The angle strain and the torsional strain in cyclopropane make this ring size extremely reactive. The conformation of cyclopentane is slightly folded, like the shape of an envelope. The chair conformation of cyclohexane has one methylene group puckered upward and another puckered downward.

Compare this actual structure with the hypothetical planar structure in Figure This interference is called a 1,3-diaxial interaction. Conformations of Cyclopropane Caption: The angle compression of cyclopropane is Conformations of Cyclohexane Caption: The more stable conformation has both methyl groups in equatorial positions. Regardless of the other groups present, the most stable conformation has a t-butyl conformaional in an equatorial position.

Much like ethane the staggered conformations of propane is lower in energy than the eclipsed conformations. The conformation connformacional cyclobutane is slightly folded. Conformational Analysis of Ethane 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.