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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For butane there will be two different staggered conformations: The following figure shows the severe steric interactions in a chair ciclloalcanos with a t-butyl group axial. Newman Projections of Butane Caption: An equatorial methyl group will be anti to the C3.

Cyclohexane can adopt four non-planar conformations: Torsional energy of butane. Esta interferencia es llamada interacciones 1,3-diaxial. The other eclipsed conformations are lower in energy than the totally eclipsed conformation but are still more unstable than the staggered conformations. Either of the chair conformations of trans-1,3-dimethylcyclohexane has one methyl group in an axial position and one in an equatorial position.

Some common alkyl groups and their names. Conformational Energy Diagram of Cyclohexane Caption: In this case both chairs have the same energy, and they are present in equal amounts. Nomenclature of Alkyl Groups Caption: Often, the longest chain with the most substituents is not obvious.

El Cis-1,3-dimetilciclohexano puede tener ambos grupos axiales o ecuatoriales.

Estructura y Estereoquímica de Alcanos

As they are numbered here, the odd-numbered carbons have their upward bonds axial and their downward bonds equatorial. Conformational Analysis of Propane Caption: The equatorial bonds are directed outward, toward the equator of the ring. At room temperature, this barrier is easily overcome, and the molecules rotate constantly.

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The cicloalcanps of cyclopentane is slightly folded, like the shape of an envelope. Chair Conformations of trans-1,3-Dimethylcyclohexane Caption: Much like ethane the staggered conformations of isomeriq is lower in energy than the eclipsed conformations. Viewed from the Newman projection, the chair conformation has no eclipsing of the carbon-carbon bonds.

Angle Strain in Cyclopropane Caption: Substituents on a carbon chain are called alkyl groups. Newman Projection of Methylcyclohexane: To make this website work, we log user data and share it with processors. The eclipsed conformations are higher in energy than the staggered conformations of butane, especially the totally eclipsed conformation.

Alkanes with an even number of carbons pack better than those with an odd number of carbons. Three of these conformations are given specific names. Cyclohexanes with tertiary-butyl substituents show that an axial t-butyl group is severely hindered. The torsional energy of ethane is lowest in the staggered conformation. Some groups are so bulky that they are extremely hindered in axial positions.

Isomería – Wikipedia

Ambas conformaciones tienen un metil axial y otro ecuatorial. Compare this actual structure with the hypothetical planar structure in Figure The simplest alkane is methane, CH4.

Axial hydrogens are pointed straight up or down, parallel to the axis of the ring. When looking for the longest continuous chain, look to find all the different chains of that length. In the symmetrical boat conformation conformaciohal cyclohexane, eclipsing of bonds results in torsional strain.

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Chair Conformation of Cyclohexane Caption: Looking down the C1-C2 bond of the equatorial conformation, we find that the methyl group is anti to C3. The axial bonds are directed vertically, parallel to the axis of the ring.

The Newman projection is the best way to judge the stability of the different conformations of a molecule. Chair interconversion would still produce an axial and an equatorial methyl. Groups like tert-butyl are so bulky that it will force the chair conformation where it is in the equatorial position, regardless of other groups present. To use this website, you must agree to our Privacy Policyincluding cookie policy.

The Newman Projection of Propane Caption: This conformation is lower in energy and favored over the conformation with the methyl in the axial position. To convert between these two conformations, the molecule must pass through the zlcanos half-chair conformation. Alkyl substituents on cyclohexane isimeria will tend to be equatorial to avoid 1,3-diaxial interactions.

Torsional energy of propane. The unfavorable conformation has both methyl groups in axial positions, with a 1,3-diaxial interaction between them. Conformations with Extremely Bulky Groups Caption: This puckered conformation reduces the eclipsing of adjacent CH2 groups.