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The vector stencils library "Conformations" contains 32 symbols of ring conformations, Newman and Fisher projections for chemical and biochemical drawing the molecular models and structural formulas of organic molecules and biochemical metabolites, the conformers spatial structures of organic molecules, the schemes of stereospecific chemical reactions in organic synthesis.
Use these shapes to draw your stereochemistry drawings in the ConceptDraw PRO diagramming and vector drawing software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
www.conceptdraw.com/ solution-park/ science-education-chemistry
Cyclohexane: boat conformation
Cyclohexane: boat conformation, cyclohexane, boat conformation,
Cyclohexane: chair conformation
Cyclohexane: chair conformation, cyclohexane, chair conformation,
Cyclopentane: envelope conformation
Cyclopentane: envelope conformation, cyclopentane, envelope conformation,
Cyclopentane: envelope conformation
Cyclopentane: envelope conformation, cyclopentane, envelope conformation,
Cyclobutane: saddle conformation
Cyclobutane: saddle conformation, cyclobutane, saddle conformation,
Cyclobutane: saddle conformation
Cyclobutane: saddle conformation, cyclobutane, saddle conformation,
Fischer projection formula
Fischer projection formula, Fischer projection formula, monosaccharide,
Fischer projection formula
Fischer projection formula, Fischer projection formula, monosaccharide,
Fischer projection formula
Fischer projection formula, Fischer projection formula, monosaccharide,
Pyranose cycle
Pyranose cycle, pyranose cycle, pyranose, Haworth formula, monosaccharide,
Pyranose cycle
Pyranose cycle, pyranose cycle, pyranose, Haworth formula, monosaccharide,
Furanose cycle
Furanose cycle, furanose cycle, furanose, Haworth formula, monosaccharide,
Furanose cycle
Furanose cycle, furanose cycle, furanose, Haworth formula, monosaccharide,
Furanose cycle
Furanose cycle, furanose cycle, furanose, Haworth formula, monosaccharide,
Furanose cycle
Furanose cycle, furanose cycle, furanose, Haworth formula, monosaccharide,
Cyclobutane
Cyclobutane, cyclobutane,
Cyclopropane
Cyclopropane, cyclopropane,
Cyclopropane
Cyclopropane, cyclopropane,
Conformation
Conformation, conformation,
Conformation
Conformation, conformation,
Newman projection formula
Newman projection formula, Newman projection formula,
Newman projection formula
Newman projection formula, Newman projection formula,
Cyclohexane: twist-boat
Cyclohexane: twist-boat, cyclohexane, twist-boat conformation,
Cyclohexane: twist-chair
Cyclohexane: twist-chair, cyclohexane, twist-chair conformation,
Cyclohexane: planar form
Cyclohexane: planar form, cyclohexane, planar form,
Cyclohexane: equatorial form
Cyclohexane: equatorial form, cyclohexane, equatorial form,
Cycloheptane: chair conformation
Cycloheptane: chair conformation, cycloheptane, chair conformation,
Cycloheptane: boat conformation
Cycloheptane: boat conformation, cycloheptane, boat conformation,
Cycloheptane: equatorial form
Cycloheptane: equatorial form, cycloheptane, equatorial form,
Cyclooctane: chair conformation
Cyclooctane: chair conformation, cyclooctane, chair conformation,
Cyclooctane: boat conformation
Cyclooctane: boat conformation, cyclooctane, boat conformation,
Cyclooctane: equatorial form
Cyclooctane: equatorial form, cyclooctane, equatorial form,
Used Solutions
The vector stencils library "Conformations" contains 32 symbols of ring conformations, Newman and Fisher projections for chemical and biochemical drawing the molecular models and structural formulas of organic molecules and biochemical metabolites. It is useful in stereochemistry for drawing spatial structures of conformers of organic molecules, and schemes of stereospecific chemical reactions in organic synthesis.
"In chemistry, conformational isomerism is a form of stereoisomerism in which the isomers can be interconverted exclusively by rotations about formally single bonds (refer to figure on single bond rotation). Such isomers are generally referred to as conformational isomers or conformers and, specifically, as rotamers. Rotations about single bonds are restricted by a rotational energy barrier which must be overcome to interconvert one conformer to another. Conformational isomerism arises when the rotation about a single bond is relatively unhindered. That is, the energy barrier must be small enough for the interconversion to occur.
Conformational isomers are thus distinct from the other classes of stereoisomers (i. e. configurational isomers) where interconversion necessarily involves breaking and reforming of chemical bonds. For example, L- & D and R- & S- configurations of organic molecules have different handedness and optical activities, and can only be interconverted by breaking one or more bonds connected to the chiral atom and reforming a similar bond in a different direction or spatial orientation.
The study of the energetics between different rotamers is referred to as conformational analysis. It is useful for understanding the stability of different isomers, for example, by taking into account the spatial orientation and through-space interactions of substituents. In addition, conformational analysis can be used to predict and explain product(s) selectivity, mechanisms, and rates of reactions." [Conformational isomerism. Wikipedia]
The chemical symbols example "Design elements - Conformations" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
Molecular conformations and projections
Molecular conformations and projections, pyranose cycle, pyranose, Haworth formula, monosaccharide, furanose cycle, furanose, Haworth formula, monosaccharide, cyclopropane, cyclopentane, envelope conformation, cyclooctane, equatorial form, cyclooctane, chair conformation, cyclooctane, boat conformation, cyclohexane, twist-chair conformation, cyclohexane, twist-boat conformation, cyclohexane, planar form, cyclohexane, equatorial form, cyclohexane, chair conformation, cyclohexane, boat conformation, cycloheptane, equatorial form, cycloheptane, chair conformation, cycloheptane, boat conformation, cyclobutane, saddle conformation, cyclobutane, conformation, Newman projection formula, Fischer projection formula, monosaccharide,
Used Solutions