Abstract
Like cyclohexane derivatives, the glucopyranose ring may have the chair or boat conformation [2]. It is generally accepted that the more stable conformation of cyclohexane is the chair one with D3d-symmetry (Fig. II.15). The bonds parallel to the C3-axis are usually called axial (a), those forming a tetrahedral angle with this axis—equatorial (e). The cyclohexane ring actually is not tetrahedral and the endocyclic angle C-C-C seems to be 111.5° (Fig. II.16). With regard to this value the torsion angle C-C-C (ϕ) happens to be 54.5°. The torsion angle between the adjacent axial and equatorial bonds is also 54.5°. Taking into account that the H-C-H angles in cyclohexane are less than tetrahedral the value of the projection angle H-C-H (ω) is accepted as being 118°.
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© 1991 Springer-Verlag Berlin Heidelberg
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Tarchevsky, I.A., Marchenko, G.N. (1991). Cellulose Conformation. In: Cellulose: Biosynthesis and Structure. Heidelberger Lehrtexte Wirtschaftswissenschaften. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-75474-6_15
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DOI: https://doi.org/10.1007/978-3-642-75474-6_15
Publisher Name: Springer, Berlin, Heidelberg
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