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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Cicloalcabos unfavorable conformation has both methyl groups in axial positions, with a 1,3-diaxial interaction between them. Newman Projection of Methylcyclohexane: To convert between these two conformations, the molecule must pass through the unstable half-chair conformation.

Some groups are so bulky that they are extremely hindered in axial positions. Some conformations can be more stable than others. 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.

Conformational Analysis of Ethane Caption: The simplest alkane is methane, CH4.

Estructura y Estereoquímica de Alcanos

Boat Conformation of Cyclohexane Caption: Conformational Energy Diagram of Cyclohexane Caption: Since the methyl group occupies more space than a hydrogen, the torsional strain will be 0. Alkyl substituents on cyclohexane rings will tend to be equatorial to conrormacional 1,3-diaxial interactions. This interference is called a 1,3-diaxial interaction. Cyclohexane can adopt four non-planar conformations: The chair conformation is most stable, followed by the twist boat.

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The C-C bond distance is 1. Groups like tert-butyl are so bulky dicloalcanos it will force the chair conformation where it is in the equatorial position, regardless of other groups present. Esta interferencia es llamada interacciones 1,3-diaxial.

The different arrangement formed by rotations about a single bond are called conformations, and a specific is called conformer. The methyl group is axial in one conformation, and equatorial in the other. Solution The longest carbon chain contains eight carbon atoms, so this compound is named as an octane. Torsional strain in cyclopropane. The chair conformation of cyclohexane has one methylene group puckered conformacionall and another puckered downward.

Folding gives partial relief from the eclipsing of bonds, as shown in the Newman projection. The Newman projection looks straight down the carbon-carbon bond. Longer chained alkanes have greater surface area and can have more surface contact and more induced dipoles than branched alkanes with smaller surface areas.

Regardless of ksomeria other groups present, the most stable conformation has a t-butyl group in an equatorial position.

Alcanos y Cicloalcanos by Adrian Marcelo Giurno on Prezi

Comparison of the boiling points of the unbranched alkanes blue with those of some branched alkanes red. They are named by replacing the -ane ending of the alkane with -yl. The conformation of cyclopentane is slightly folded, like the shape of an envelope. Chair Conformations of trans-1,3-Dimethylcyclohexane Caption: The totally eclipsed cidloalcanos is about 1. The Newman projection is the best way to judge the stability of the different conformations of a molecule.

The conformation of cyclobutane is slightly folded. Isomerja is steric hindrance between these hydrogens so the molecule twists a little producing the twist boat conformation which is 1. Nomenclature of Alkyl Groups Caption: The staggered conformations are lower in ciicloalcanos than the eclipsed conformation because the staggering allows the electron clouds of the C-H bonds to be as far apart as possible.

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Propane is shown here as a perspective drawing and as a Newman projection looking down aclanos of the carbon-carbon bonds. Either of the chair conformations of trans-1,3-dimethylcyclohexane has one methyl group in an axial position and one in an equatorial position.

The following figure shows the severe steric interactions in a chair conformation with a t-butyl group axial. Cyclobutane adopts the folded conformation to decrease the torsional strain caused by eclipsing hydrogens.

When molecules can pack in neat order avoiding empty pockets the melting point will be higher than when the packing is not ordered. To make this website work, we log user data and share it with processors.

In isomeira case both chairs have the same energy, and they are present in equal amounts. C5H12 C H 3 2 n-pentano iso-pentano neo-pentano Chapter 3.

The angle strain and the torsional strain in cyclopropane make this ring size extremely reactive. The molecular formula of alkanes is CnH2n, two hydrogen less than an open chain alkane.

The eclipsed conformation is about 3. Totally Eclipsed Conformation of Butane Caption: Butano tiene 2 conformaciones alternadas diferentes: