Staggered Conformation
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Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. In organic chemistry a staggered conformation is a chemical conformation of an ethane-like moiety abcX-Ydef in which the substituents a,b,and c are at the maximum distance from d,e,and f. This requires the torsion angles to be 60°. Such a conformation exists in any open chain single chemical bond connecting two sp3 hybridised atoms, and is normally a conformational energy minimum.For some molecules such as those of n-butane, there can be special versions of staggered conformations called gauche and anti; see first Newman projection diagram in Conformational isomerism.
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. In organic chemistry a staggered conformation is a chemical conformation of an ethane-like moiety abcX-Ydef in which the substituents a,b,and c are at the maximum distance from d,e,and f. This requires the torsion angles to be 60°. Such a conformation exists in any open chain single chemical bond connecting two sp3 hybridised atoms, and is normally a conformational energy minimum.For some molecules such as those of n-butane, there can be special versions of staggered conformations called gauche and anti; see first Newman projection diagram in Conformational isomerism.
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