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Fluorene resonance structures

Fig. 5 Fully conjugated indeno[l,2-h]fluorene 2 and resonance structures of 22... Fig. 5 Fully conjugated indeno[l,2-h]fluorene 2 and resonance structures of 22...
The hydrocarbon with the common name fluorene is acidic enough (p a = 23) to be a useful indicator in deprotonation reactions of compounds of greater acidity. Indicate the most acidic hydrogen(s) in fluorene. Draw resonance structures to explain the relative stability of its conjugate base. [Pg.1031]

A methylene group resonance which joins two ring structures (bridgehead) appears at lower magnetic field, Table 3. The singlets at 3.36 and 3.88 ppm in Fraction K can be assigned to acenaphthene and fluorene, respectively. [Pg.298]


See other pages where Fluorene resonance structures is mentioned: [Pg.424]    [Pg.51]    [Pg.901]    [Pg.1332]    [Pg.174]    [Pg.424]    [Pg.444]    [Pg.130]    [Pg.137]    [Pg.158]    [Pg.95]    [Pg.80]    [Pg.25]    [Pg.172]    [Pg.279]    [Pg.429]    [Pg.174]    [Pg.26]    [Pg.592]    [Pg.592]    [Pg.467]    [Pg.63]    [Pg.273]   
See also in sourсe #XX -- [ Pg.214 ]

See also in sourсe #XX -- [ Pg.214 ]




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