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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Solution The longest carbon chain contains eight carbon atoms, so this compound is named as an octane.

Angle strain in cyclopropane. Axial hydrogens are pointed straight up alcanoa down, parallel to the axis of the ring. Conformational Analysis of Butane Caption: The axial bonds are directed vertically, parallel to the axis of the ring.

Alcanos y Cicloalcanos by Adrian Marcelo Giurno on Prezi

The six-membered rings in cis- and trans-decalin assume chair conformations. The staggered conformations are lower in energy than the eclipsed conformation conformavional the staggering allows the electron clouds of the C-H bonds to be as far apart as possible.

To make this website work, we log user data and share it with processors. The four hydrogen atoms are covalently bonded to the central carbon atom, with bond lengths of 1.

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There is steric hindrance between these hydrogens so the molecule twists a little producing the twist boat conformation which is 1. When there are two carbon chains of the same length, the one that has the most substituents must be chosen to name the compound. Pure conformers cannot be isolated in most cases, because the molecules are constantly rotating through all the possible conformations. The conformation of wlcanos is slightly folded, like the shape of an envelope.

Estructura y Estereoquímica de Alcanos

Alcanoos Analysis of Propane Caption: In the symmetrical boat conformation of cyclohexane, eclipsing of bonds results in torsional strain. The angle strain and the torsional strain in cyclopropane make this ring size extremely reactive.

The only intermolecular force of nonpolar molecules are London dispersion forces which result from induced dipole attractions.

Boat Conformation of Cyclohexane Caption: The different arrangement formed by rotations about a single bond are called conformations, and a specific is ieomeria conformer.

All the carbon-carbon bonds are eclipsed, generating torsional strain that contributes to the total ring strain.

C5H12 C H 3 2 n-pentano iso-pentano neo-pentano Chapter 3. Looking down the C1-C2 bond of the equatorial conformation, we find that the methyl group is anti to C3. At room conformaciobal, this barrier is easily overcome, and the molecules rotate constantly.

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The conformation of cyclobutane is slightly folded. Torsional energy of butane. In the Newman projection it is easier to see the steric interaction between the methyl substituent and the hydrogens and carbons of the ring.

Conformations of Cyclopentane Caption: There are two possible geometric isomers for decalin: Some groups are so bulky that they are extremely hindered conformcaional axial positions.

Angle Strain in Cyclopropane Caption: Folding gives partial relief from the eclipsing of bonds, as shown in the Newman projection. Cicloalcqnos can adopt four non-planar conformations: Cyclobutane adopts the folded conformation to decrease the torsional strain caused by eclipsing hydrogens.

Isomería – Wikipedia

This conformation is lower in energy and favored over the conformation with the methyl in the axial position. In solids, the packing of the molecules into a three dimensional structure affects the melting point. The more stable conformation has both methyl groups in equatorial positions.