isomer$41073$ - translation to spanish
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isomer$41073$ - translation to spanish

TYPE OF CHEMICAL ISOMERISM
Endo conformer; Endo isomer; Exo isomer

isomer      
n. isómero (compuesto químico con las mismas características de otro compuesto excepto una distinta estructura molecular)
isomeric         
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  • Molecular models of cyclohexane in boat and chair conformations.  The carbon atoms are colored amber or blue according to whether they lie above or below the mean plane of the ring. The C–C bonds on the ring are light green.
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  • O}}: '''I''' 1-propanol, '''II''' 2-propanol, '''III''' ethyl-methyl-ether.
MOLECULE WITH IDENTICAL ATOMIC COMPOSITION AS ANOTHER, BUT WITH DIFFERENT STRUCTURES OR ORIENTATIONS
Isomers; Isomeric; Isomerism; Molecular isomerism; Chemical isomer; Isomerizing; Isomerized
(adj.) = isomérico
Ex: The new centric indexes may be used for topological correlations, for estimating the topological shape of isomeric chemical structures, and for use in coding and computer processing of chemical information.
isomer         
  • 150px
  • Molecular models of cyclohexane in boat and chair conformations.  The carbon atoms are colored amber or blue according to whether they lie above or below the mean plane of the ring. The C–C bonds on the ring are light green.
  • center
  • center
  • 120px
  • 120px
  • 150px
  • O}}: '''I''' 1-propanol, '''II''' 2-propanol, '''III''' ethyl-methyl-ether.
MOLECULE WITH IDENTICAL ATOMIC COMPOSITION AS ANOTHER, BUT WITH DIFFERENT STRUCTURES OR ORIENTATIONS
Isomers; Isomeric; Isomerism; Molecular isomerism; Chemical isomer; Isomerizing; Isomerized
(n.) = isómero
Ex: Even more severe problems arise when we consider isomers: compounds containing the same atoms in each molecule, but differently arranged.

Definition

Isomerism
·noun The state, quality, or relation, of two or more isomeric substances.

Wikipedia

Endo-exo isomerism

In organic chemistry, endoexo isomerism is a special type of stereoisomerism found in organic compounds with a substituent on a bridged ring system. The prefix endo is reserved for the isomer with the substituent located closest, or "syn", to the longest bridge. The prefix exo is reserved for the isomer with the substituent located farthest, or "anti", to the longest bridge. Here "longest" and "shortest" refer to the number of atoms that comprise the bridge. This type of molecular geometry is found in norbornane systems such as dicyclopentadiene.

The terms endo and exo are used in a similar sense in discussions of the stereoselectivity in Diels–Alder reactions.