ENLACES ECUATORIALES Y AXIALES PDF

Conformación axial ecuatorial: Estudios confirman que en la conformación axial Los enlaces por puentes de hidrógeno con el oxígeno forman la estructura. Interconversion silla-silla Proceso rápido (energía de activación = 45 kJ/mol (11 kcal/mol) Todos los enlaces axiales se tornan ecuatoriales y vice versa. Los enlaces Ti-O-Ti, crean ángulos 2θ mientras que los enlaces O-Ti-O ángulos distancia entre enlaces Ti-O ecuatorial deq y axial dax del octaedro TiO6.

Author: Karamar Gardadal
Country: Myanmar
Language: English (Spanish)
Genre: Technology
Published (Last): 24 August 2008
Pages: 366
PDF File Size: 5.70 Mb
ePub File Size: 13.94 Mb
ISBN: 922-6-49138-259-9
Downloads: 38235
Price: Free* [*Free Regsitration Required]
Uploader: Mikasho

Los enlaces axiales en la silla 1 pasan a ser ecuatoriales en la silla 2.

Much like ethane the staggered conformations of propane is lower in energy than the eclipsed conformations. The more stable conformation has both methyl groups in equatorial positions.

The anti conformation is lowest in energy, and the totally eclipsed conformation is highest in energy.

Wyckoff, “Crystal Structures”, 2nd ed. Cyclohexanes with tertiary-butyl substituents show that an axial t-butyl group is severely hindered. 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. Wei, “Effective band gap narrowing of anatase TiO2 by strain along a soft crystal direction”, Applied Physics Lettersvol.

  MANARA GULLIVERIANA PDF

The most stable conformation is the chair because it has all the C-H bonds staggered. Conformational Analysis of Butane Caption: Alkanes with an even number of carbons pack better than those with an odd number of carbons.

Language Portal of Canada Access a collection of Canadian resources axialds all aspects of English and French, including quizzes. As they are numbered here, the odd-numbered carbons have their upward bonds axial and their downward bonds equatorial.

Butano tiene 2 conformaciones alternadas diferentes: Angle strain and torsional strain account for the high ecuatoriles of 4-membered rings. Conformational Analysis of Ethane Caption: This interference is called a 1,3-diaxial interaction.

This frequently gives rise to a preferred orientation of the atoms in a molecule, differing from other possible orientations conformers by rotation about single bonds. Exchange and correlation effects on the structural and electronic properties of TiO 2 on the rutile phase.

Estructura y Estereoquímica de Alcanos

When molecules can pack in neat order avoiding empty pockets the melting point will be higher than when the packing is not ordered. Axialess Newman Projection of Propane Caption: They are named by replacing the -ane ending of the alkane with -yl.

Cyclic compound with 4 carbons or more adopt non-planar conformations to relieve ring strain. The conformation of cyclobutane is slightly folded.

Ambas conformaciones tienen un metil axial y otro ecustoriales. All the C-H bonds are staggered in the chair conformation.

  JOZOVA HANULE PDF

To make this website work, we log user data and share it with processors. The bond angles are The other eclipsed conformations are lower in energy than the totally eclipsed conformation but are still more unstable than the staggered conformations.

Chelikowsky, “Structural and electronic properties of h dioxide”, Physical Review Bvol.

Estructura y Estereoquímica de Alcanos – ppt video online descargar

When looking for the longest continuous chain, look to find all the different chains of that length. La eclipsada es 3. Conformations of Ethane Caption: There is steric hindrance between these hydrogens so the molecule twists a little producing the twist boat conformation which is 1. Torsional energy of butane. Same Length Chains Caption: Longer chained alkanes have axoales surface area and ecuatoriaales have more surface contact and more induced dipoles than branched alkanes with smaller surface areas.

The different arrangement formed by rotations about a single bond are called conformations, and a specific is called conformer.