Os alcanos son hidrocarburos, é dicir que teñen só átomos de carbono e .. difiren en enerxía: a conformación alternada é 12,6 kJ/mol menor en enerxía (por . Presentación del tema: “Estructura y Estereoquímica de Alcanos”— . Conformaciones son diferentes arreglos de los átomos producidos al rotar el enlace σ. Análisis conformacional del etano Análisis conformacional del butano Mecánica molecular aplicada a los alcanos y los cicloalcanos

Author: Tolmaran Gak
Country: Malawi
Language: English (Spanish)
Genre: Finance
Published (Last): 13 November 2014
Pages: 16
PDF File Size: 1.89 Mb
ePub File Size: 13.20 Mb
ISBN: 630-6-24446-346-7
Downloads: 22142
Price: Free* [*Free Regsitration Required]
Uploader: Faeshicage

Conformations of Cyclohexane Caption: Angle Strain in Cyclopropane Caption: Alcohols are compounds whose molecules have a hydroxyl. C5H12 C H 3 2 n-pentano iso-pentano neo-pentano Chapter 3. Ambas conformaciones tienen un metil axial y otro ecuatorial. 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. Newman Projection of Methylcyclohexane: Pure conformers cannot be isolated in most cases, because the molecules are constantly rotating through all the possible conformations.

Their physical properties resemble those of alkanes. To use this website, you must agree to our Privacy Policyincluding cookie policy. Some groups are so bulky that they are extremely hindered in axial positions.

Structures of some cycloalkanes. When looking for the longest continuous chain, look to find all the different chains of that length.

Análisis conformacional by Química Orgánica on Prezi

For butane there will be two different staggered conformations: Los botones se encuentran debajo. The following figure shows the severe steric interactions in a chair conformation with a t-butyl group axial. The bond angles are Interconversion between conformzciones conformations require that cyclohexane go through its higher energy conformations. Cyclic compound with 4 carbons or more adopt non-planar conformations to relieve ring strain.


Groups like tert-butyl are so bulky that it will force the chair conformation where it conformacciones in the equatorial position, regardless of other groups present. Conformational energy of cyclohexane.

In solids, the packing of the molecules into a three dimensional structure affects the melting point. Folding gives partial relief from the eclipsing of bonds, as shown in the Newman projection. There is steric hindrance between these hydrogens so the molecule twists a little producing the twist boat conformation which is 1.

The even-numbered carbons have their downward bonds axial and their upward bonds equatorial. Conformations with Extremely Bulky Groups Caption: The simplest alkane is methane, CH4. Torsional energy of butane.


When molecules can pack in conformaciohes order avoiding empty pockets the melting point will be higher than when the packing is not ordered. Angle strain in cyclopropane. Angle strain and torsional strain account for the high reactivity of 4-membered rings.

Torsional strain in cyclopropane. Conformations of Cyclopropane Caption: Ethane has two sp3 carbons. Compare this actual structure with the hypothetical planar structure in Figure The Newman projection looks straight down the carbon-carbon bond.


Chair Conformations of trans-1,3-Dimethylcyclohexane Caption: When there are two carbon chains of the same length, the one that has the most substituents must be chosen to name the compound.

Comparison of the boiling points of the unbranched alkanes blue alcanoz those of some branched alkanes red.

The more stable conformation has both methyl groups in equatorial positions. The molecular formula of alkanes is CnH2n, two hydrogen less than an open chain alkane.

An error occurred.

The most stable conformation is the chair because it has all the C-H bonds staggered. Much like ethane the staggered conformations of propane is lower in energy than the eclipsed conformations.

Substituents on a carbon chain are called alkyl groups. Alkanes with an even number of carbons pack better than those with an odd number of carbons.

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.

Conformmaciones substituents on cyclohexane rings will tend to be equatorial to avoid 1,3-diaxial interactions. Because of their smaller surface areas, branched alkanes have lower boiling points than unbranched alkanes.