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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Either of the chair conformations of trans-1,3-dimethylcyclohexane has one methyl group in an axial position and one in an equatorial position. Conformational Analysis of Ethane Caption: Alcanos con par de C tienen p.

Estructura y Estereoquímica de Alcanos

To relieve ring strain, cyclopentane adopts the envelope conformation. This kind of interference between two bulky groups is called steric strain or steric hindrance. La eclipsada es 3. Conformations of Cyclohexane Caption: Esta interferencia es llamada interacciones 1,3-diaxial.

Totally Eclipsed Conformation of Butane Caption: Chair Lsomeria of Cyclohexane Caption: The Newman projection looks alcanks down the carbon-carbon bond. Same Length Chains Caption: Cyclohexanes with tertiary-butyl substituents show that an axial t-butyl group is severely hindered. The conformation of cyclobutane is slightly folded. The angle strain and the torsional strain in cyclopropane make this ring size extremely reactive.

Cyclic compound with 4 carbons or more adopt non-planar conformations to relieve ring strain.


Structures of conformafional cycloalkanes. Cyclohexane can adopt four non-planar conformations: An equatorial methyl group will be anti to the C3. The anti conformation is lowest in energy, and the totally eclipsed conformation is highest in energy. When looking for the longest continuous chain, look to find all the different chains of that length.

The chair conformation of cyclohexane has one methylene group puckered upward and another puckered downward. Often, the longest chain with the most substituents is not obvious. Their physical properties resemble those of alkanes.

Interconversion between chair conformations require that cyclohexane go cilcoalcanos its higher energy conformations. The angle compression for alcnos is Pure conformers cannot be isolated in most cases, because the molecules are constantly rotating through all the possible conformations.

This conformation is lower in energy and favored over the conformation with the methyl in the axial position. Any carbon with four sigma bonds has an sp3 hybridization. Chair Conformations of cis-1,3-Dimethylcyclohexane Caption: The eclipsed conformation is about 3. Conformations of Conformaiconal Caption: Chair interconversion would still produce an axial and an equatorial methyl. At room temperature, this barrier is easily overcome, and the molecules rotate constantly.

The Newman projection is the best way to judge the stability of the different conformations of a molecule. The more stable conformation has both methyl groups in equatorial positions.

Conformational energy of cyclohexane. The eclipsed conformations are higher in energy than the staggered conformations of butane, especially the totally eclipsed conformation. Ciclaolcanos of their smaller surface areas, branched alkanes have lower boiling points than unbranched alkanes. Alcanos ramificados tienen p. Solution The longest carbon chain contains eight carbon atoms, so this compound is named as an octane.


Isomería – Wikipedia

The conformation of cyclopentane is slightly folded, like the shape of an envelope. Three of these conformations are ksomeria specific names. Boat Conformation of Cyclohexane Caption: Propane is shown here as a perspective drawing and as a Newman projection looking down one of the carbon-carbon bonds. Los substituyentes axiales interfieren con los H axiales del C 3 y C 5. The totally eclipsed conformation is about 1. Conformations of Cyclobutane Caption: Alkyl substituents on cyclohexane rings will tend to be equatorial to avoid 1,3-diaxial interactions.

Alcanos y Cicloalcanos by Adrian Marcelo Giurno on Prezi

The other eclipsed conformations are lower in energy than the totally eclipsed conformation but are still more unstable than the staggered conformations. In the Newman projection it is easier to see the steric interaction between the methyl substituent and the hydrogens and carbons of the ring. The axial substituent interferes with the axial hydrogens on C3 and C5. The Newman Projection of Propane Caption: