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Cyclopropane structural chemistry

Since both structures 6 and 7 are highly unstable, we can conclude that the cyclopropane structure 1 is by far the most stable cyclic C3H6 system possible. It complies with the rules of classical carbon chemistry [tetravalent C, (distorted) tetragonal geometries] and, therefore, it is relatively stable. [Pg.47]


See other pages where Cyclopropane structural chemistry is mentioned: [Pg.1109]    [Pg.16]    [Pg.141]    [Pg.143]    [Pg.145]    [Pg.147]    [Pg.149]    [Pg.151]    [Pg.153]    [Pg.155]    [Pg.157]    [Pg.159]    [Pg.161]    [Pg.163]    [Pg.165]    [Pg.167]    [Pg.169]    [Pg.171]    [Pg.173]    [Pg.175]    [Pg.177]    [Pg.179]    [Pg.181]    [Pg.183]    [Pg.185]    [Pg.187]    [Pg.189]    [Pg.191]    [Pg.193]    [Pg.195]    [Pg.197]    [Pg.199]    [Pg.201]    [Pg.203]    [Pg.205]    [Pg.207]    [Pg.209]    [Pg.211]    [Pg.213]    [Pg.215]    [Pg.217]    [Pg.219]    [Pg.221]    [Pg.481]    [Pg.1010]    [Pg.1013]    [Pg.538]    [Pg.16]   
See also in sourсe #XX -- [ Pg.79 ]




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