DEFINICION DE ESTEREOQUIMICA PDF

La química en tres dimensiones se conoce como estereoquímica. En la tabla se resumen algunas definiciones básicas relacionadas con la estructura. Definición El ibuprofeno es un antiinflamatorio no esteroideo (AINE), Estereoquímica El ibuprofeno se produce industrialmente en forma de. grupos funcionales organicos estereoquimica practicas de laboratorio de la práctica deberemos conocer bien la definición de sublimación y el concepto de.

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The conformation of cyclobutane is slightly definiicon. Conformational Energy Diagram of Cyclohexane Caption: The axial bonds are directed vertically, parallel to the axis of the ring. Boat Conformation of Cyclohexane Caption: To convert between these two conformations, the molecule must pass through the unstable half-chair conformation. In this case both chairs have the same energy, and they are present in equal amounts. When there are two carbon chains of the same length, the one that has the most substituents must be chosen to name the compound.

For butane there will be two different staggered conformations: The Newman projection looks straight down the carbon-carbon bond. Some conformations can be more stable than others. They are named by replacing the -ane ending of the alkane with -yl. Cyclohexanes with tertiary-butyl substituents show that an axial t-butyl group is severely hindered.

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The Newman Projection of Propane Caption: To use this website, you must agree to our Privacy Policyincluding cookie policy. C5H12 C H 3 2 n-pentano iso-pentano neo-pentano Chapter 3.

This theme is included in the chapter “Formation of carbon-carbon double bonds” in the mentioned text. There are two possible geometric isomers for decalin: Stork, G, Raucher, S. The high reactivity of cyclopropanes is due to the non-linear overlap of the sp3 orbitals.

Chiral synthesis of prostaglandins from carbohydrates. Two chair conformations are possible for edfinicion. Alkanes with an even number of carbons pack better than those with an odd number of carbons. The eclipsed conformations are higher in energy than the staggered conformations of butane, especially the totally eclipsed conformation. An equatorial methyl group will be anti to the Esterekquimica.

Hemos propuesto mecanismos para este hecho. We also covered from a mechanistic stand point the theme estereoquiimica the geometry of the enol ether double bond and its control by means of the procedure described by Ireland. Ethane has two sp3 carbons.

Estructura y Estereoquímica de Alcanos

Torsional energy estereoqiumica butane. Any of the configurations at the chiral carbon formed C-3 in 2 or 4 can be obtained if a change in the stereochemistry of double bond of the allylic portion is done. Same Length Chains Caption: This puckered conformation reduces the eclipsing of adjacent CH2 groups.

Structures of some cycloalkanes. The configuration at C-3 of the product 2 or 4 comes from directly from the starting reagent [11], see Fig. The angle strain and the torsional strain in cyclopropane make this ring size extremely definiion.

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When a bond of propane rotates, the torsional energy varies much like it does in ethane, but with 0. Estereoqiumica of Cyclopropane Caption: The ring strain of a planar cyclobutane results from two factors: During master classes of organic chemistry we noticed that students are confronted with a lack of knowledge with regard to mechanisms.

Their physical properties resemble those of alkanes. At least three chiral centers may be involved in the rearrangement.

Chair-chair interconversion of methylcyclohexane. The axial substituent interferes with the axial hydrogens on C3 and C5.

Estereoquimica by Alejandro Villalobos on Prezi

Melting Points of Alkanes Caption: The chair conformation is most stable, followed by the twist boat. Alkyl substituents on cyclohexane rings will tend to be equatorial to avoid 1,3-diaxial interactions.

Estereoquimicz angle compression of cyclopropane is Theoretical mechanistic approach to diasteroselective synthesis of cis-1,2-dialkenylcyclopropanols and subsequent oxy-Cope rearrangement by Jin Kun Cha et al, Rev. Conformations of Cyclopentane Caption: