ISOMERIA CONFORMACIONAL DE ALCANOS Y CICLOALCANOS PDF

View alcanos_ from CIENCIAS D at Marista University of Guadalajara. Estructura y conformaciones de los alcanos Conformacin Eclipsada. Estereoqumica de Cicloalcanos disustituidos: ESTABILIDAD DE LOS CICLOALCANOS Adolf. Calores de combustión: Alcano + Oxígeno Geometría molecular, Isomería conformacional, Conformación del ciclohexano, Tensión angular. La isomería ye una propiedá d’aquellos compuestos químicos n’especial les pero’l ciclohexano ye un alcano cíclicu o cicloalcano y el 1-hexeno ye un alqueno. . Los isómeros conformacionales xeneralmente nun son xebrables o.

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Esta interferencia es llamada interacciones 1,3-diaxial. Los substituyentes axiales interfieren con los H axiales del C 3 y C 5.

Alkyl alcannos on cyclohexane rings will tend to be equatorial to avoid 1,3-diaxial interactions. Propane is shown here as a perspective drawing and as a Newman projection looking down one of the carbon-carbon bonds.

Estructura y Estereoquímica de Alcanos

The totally cciloalcanos conformation is about 1. Idomeria gives partial relief from the eclipsing of bonds, as shown in the Newman projection. The unfavorable conformation has both methyl groups in axial positions, with a 1,3-diaxial interaction between them.

When a bond of propane rotates, the torsional energy varies much like it does in ethane, but with 0. The bond angles are Melting Points of Alkanes Caption: This puckered conformation reduces the eclipsing of adjacent CH2 groups.

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Groups like tert-butyl are so bulky that it will force the chair conformation where it is in the equatorial position, regardless conformacoinal other groups present. To convert between these two conformations, the molecule must pass through the unstable half-chair conformation.

Isomería – Wikipedia

Interconversion between chair conformations require that cyclohexane go through its isomwria energy conformations. Pure conformers cannot be isolated in most cases, because the molecules are constantly rotating through all the possible conformations. Because of their smaller surface areas, branched alkanes have lower boiling points than unbranched alkanes. Conformational Analysis of Ethane Caption: Alcohols are compounds whose molecules have a hydroxyl.

Conformations with Extremely Bulky Groups Caption: Ambas conformaciones tienen un metil axial y otro ecuatorial.

Angle strain in cyclopropane. The angle compression for butane is Solution The longest carbon chain contains eight carbon atoms, so this compound is named as an octane.

The Newman projection looks straight down the carbon-carbon bond. This interference is called a 1,3-diaxial interaction. As they are numbered here, the odd-numbered carbons have their upward bonds axial and their downward bonds equatorial. 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.

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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 left to right. The angle strain and the lacanos strain in cyclopropane make this ring size extremely reactive.

In the Ciclloalcanos projection it is easier to see the steric interaction between the methyl substituent and the hydrogens and carbons of the ring. Since the methyl group occupies more space than a hydrogen, the torsional strain will be 0. The even-numbered carbons have their downward bonds axial and their upward bonds equatorial.

Axial hydrogens are pointed straight up or down, parallel to the axis of the ring. Any carbon with four sigma bonds has an sp3 hybridization. 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.

Chair Conformations of cis-1,3-Dimethylcyclohexane Caption:

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