Isomeria Conformacional. fhmateo; 3 videos; 18 views; Last updated on Oct 11, Play all. Share. Loading Save. Empleo de la notación E-Z en la isomería Cis-Trans | | UPV – Duration: Universitat. Isomería de conformacional de alcanos y ciclo alcanos. Isomería conformacional (cis-trans): en dobles enlaces, en anillo.

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In solids, the packing of the molecules into a three dimensional structure affects the melting point. The conformation of cyclopentane is slightly folded, cpnformacional the shape of an envelope. Cyclohexanes with tertiary-butyl substituents show that an axial t-butyl group is severely hindered. The Newman projection looks straight down the carbon-carbon bond. For butane there will be two different staggered conformations: Conformations with Extremely Bulky Groups Caption: As they are numbered here, the odd-numbered carbons have their upward bonds axial and their downward bonds equatorial.

Nomenclature of Alkyl Groups Caption: The different arrangement formed by rotations isomreia a single bond are called conformations, and a specific is called conformer. The high reactivity of cyclopropanes is due to the non-linear overlap of the sp3 orbitals.

Conformations of Cyclopropane Caption: The simplest alkane is methane, CH4.

Isomerisme conformacional

All the carbon-carbon bonds are eclipsed, generating torsional confrmacional that contributes to the total ring strain. 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. Los substituyentes axiales interfieren con los H axiales del C 3 y C 5. In the isomeriz 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.


Los botones se encuentran debajo. Because of their smaller surface areas, branched alkanes have lower boiling points than unbranched alkanes. The anti conformation is lowest in energy, and the totally eclipsed conformation is highest in energy.

The other eclipsed conformations are lower in energy than fonformacional totally eclipsed conformation but are still more unstable than the staggered conformations.

The axial substituent interferes with the axial hydrogens on C3 and C5. Cyclohexane can adopt four non-planar conformations: When a bond of propane rotates, the torsional energy varies much like it does in conformacipnal, but with 0. Angle strain and torsional strain account for the high reactivity of 4-membered rings. In the symmetrical boat conformation of cyclohexane, eclipsing of bonds results in torsional strain.

Estructura y Estereoquímica de Alcanos – ppt video online descargar

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

The methyl group is axial in one conformation, and equatorial in the other. Longer chained alkanes have jsomeria surface area and can have more surface contact isomefia more induced dipoles than branched alkanes with smaller surface areas. All the C-H bonds are staggered in the chair conformation.


The eclipsed conformation is about 3. Alcanos ramificados tienen p.

Estructura y Estereoquímica de Alcanos

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 conformation of cyclobutane is slightly folded. The molecular formula of alkanes is CnH2n, two hydrogen less than an open chain alkane. Compare this actual structure with the hypothetical planar structure in Figure Conformational Analysis of Butane Caption: Two chair conformations are possible for cis-1,3-dimethylcyclohexane. Newman Projection of Methylcyclohexane: Sobre el proyecto SlidePlayer Condiciones de uso.

The angle strain and the torsional strain in cyclopropane make this ring size extremely reactive. Chair Isomera of cis-1,3-Dimethylcyclohexane Caption: This puckered conformation reduces the eclipsing of adjacent CH2 groups.

Conformational energy of cyclohexane. Often, the longest chain with the most substituents is not obvious.