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Cyclodecane, conformations table

Studies of cyclodecane derivatives by X-ray crystallographic methods have demonstrated that the boat-chair-boat conformation is adopted in the solid state. (Notice that boat is used here in a different sense than for cyclohexane.) As was indicated in Table 3.7 (p. 146), cyclodecane is significantly more strained than cyclohexane. Examination of the boat-chair-boat conformation reveals that the source of most of this strain is the close van der Waals contacts between two sets of three hydrogens on either side of the molecule. [Pg.148]

Some years ago, when PEF400 was new, it was applied to cyclodecane. Five conformations were selected. Three of them have been found in crystal structures Nos. 1, 2 and 4 in Table 10-3 No. 3... [Pg.127]


See other pages where Cyclodecane, conformations table is mentioned: [Pg.128]    [Pg.71]    [Pg.81]    [Pg.162]    [Pg.38]    [Pg.128]    [Pg.129]    [Pg.129]   
See also in sourсe #XX -- [ Pg.464 ]




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