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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The equatorial bonds are directed outward, toward the equator of the ring.

The torsional energy of ethane is lowest in the staggered conformation. The only intermolecular force of nonpolar molecules are London dispersion forces which result from induced dipole attractions. Chair Conformation of Issomeria Caption: When molecules can pack in neat order avoiding empty pockets the melting point will be higher than when the packing is not ordered.

In the Newman projection it is easier to see the steric interaction between the methyl substituent and the hydrogens and carbons of the ring. An equatorial methyl group will be anti to the C3. Regardless of the other groups present, the most stable conformation has a t-butyl group in an equatorial position. Boat Conformation of Cyclohexane Caption: Alkanes with an even number of carbons pack better than those with an odd number of carbons.

These conformations have equal energies, and they are present in equal amounts. Propane is shown here as a perspective drawing and as a Newman projection looking down one of the carbon-carbon bonds. Cyclohexanes with tertiary-butyl substituents show that an axial t-butyl group is severely hindered. Substituents on a carbon chain are called alkyl groups. 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.

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Two chair conformations are possible for cis-1,3-dimethylcyclohexane. The most stable conformation is the chair because it has all the C-H bonds staggered. Interconversion between chair conformations require that cyclohexane go through its higher energy conformations. 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.

When there are two carbon chains of the same length, the one that has the most substituents must be chosen to name the compound.

Estructura y Estereoquímica de Alcanos

At room temperature, this barrier is easily overcome, and the molecules rotate constantly. The angle compression of cyclopropane is Conformations of Cyclopentane Caption: To convert between these two conformations, ckcloalcanos molecule must pass through the unstable half-chair conformation. Much like ethane the staggered conformations of propane is lower in energy than the ciclialcanos conformations.

Three of these conformations are given specific names. La eclipsada es 3. Angle Strain in Cyclopropane Caption: There are two possible geometric isomers for decalin: The chair conformation of cyclohexane has one methylene group puckered upward and another puckered downward.

The six-membered rings in cis- and trans-decalin assume chair conformations. Conformations of Cyclopropane Caption: The C-C bond distance is 1. Ethane, the two-carbon alkane, is composed of two methyl groups with overlapping sp3 hybrid orbitals forming a sigma bond between them.

Estructura y Estereoquímica de Alcanos – ppt video online descargar

Often, the longest chain with the most substituents is not obvious. Pure conformers cannot be isolated in most cases, because the molecules are constantly rotating through all the possible conformations. The four hydrogen atoms are covalently bonded to the central carbon atom, with bond lengths of 1. The unfavorable conformation has both methyl groups in axial positions, with a 1,3-diaxial interaction between them.


Among the staggered conformations, the anti is lower in energy because it has the electron clouds of the methyl groups as far apart as possible.

Chair Conformations of trans-1,3-Dimethylcyclohexane Caption: Conformational energy of cyclohexane. Ambas conformaciones tienen un metil axial y otro ecuatorial.

Chair Conformations of cis-1,3-Dimethylcyclohexane Caption: In solids, the packing of the molecules into a three dimensional structure conformacioal the melting point. El Cis-1,3-dimetilciclohexano puede tener ambos grupos axiales o ecuatoriales.

Structures of some cycloalkanes. Ethane has two sp3 carbons.

Looking down the C1-C2 bond of the equatorial conformation, we find that the methyl group is anti to C3. Melting Points of Alkanes Caption: Chair-chair interconversion of methylcyclohexane.

Nomenclature of Alkyl Groups Caption: The methyl group is axial in one conformation, and equatorial in the other. Chair interconversion would still produce an axial and an equatorial methyl. Torsional energy of propane. This puckered conformation reduces the eclipsing of adjacent CH2 groups. This interference is called a 1,3-diaxial interaction. The angle compression for butane is