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C
6
H
6
138 molecule(s)
non-Kekulé molecules
non-Kekulé molecules
bicycle rearrangement
bicycle rearrangement
acenes
acid anhydrides
acid anhydrides
acylals
acyl groups
alternant
amides
amides
amidium ions
aminium ions
ammoniumyl radical ions
anilides
anilides
anilides
anthocyanidins
anti
aryl cations
arylene groups
aryl groups
axial chirality
azoxy compounds
benzylic groups
benzylic intermediates
betaines
biradical
bisphenols
catalytic dehydrocyclization
catalytic hydrogenolysis
catalytic hydrogenolysis
catalytic hydrogenolysis
catalytic hydrogenolysis
catalytic hydrogenolysis
catalytic hydrogenolysis
catecholamines
chain reaction
chain reaction
chain reaction
chain transfer
chain transfer
chain transfer
chain transfer
chain transfer
chain transfer
chain transfer
cine-substitution
cine-substitution
common-ion effect (on rates)
common-ion effect (on rates)
common-ion effect (on rates)
common-ion effect (on rates)
coumarins
cyanides
cyanine dyes
cyclic acid anhydrides (cyclic anhydrides)
cyclophanes
dehydroarenes
depsides
diazooxides
Dimroth–Reichardt
parameter
electrophile (electrophilic)
electrophile (electrophilic)
epoxy compounds
flavins
flavonoids (isoflavonoids and neoflavonoids)
flavonoids (isoflavonoids and neoflavonoids)
flavonoids (isoflavonoids and neoflavonoids)
folates
fragmentation
fragmentation
furocoumarins
furocoumarins
glycosides
helicenes
helicity
Herz compounds
heteroaryl groups
heteroarynes
heteroarynes
hyperconjugation
isocoumarins
isodesmic reaction
isodesmic reaction
isodesmic reaction
isodesmic reaction
isolated double bonds
isotope exchange
isotope exchange
isotopic scrambling
isotopic scrambling
isotopic scrambling
isotopic scrambling
isotopic scrambling
isotopic scrambling
Kekulé structure (for aromatic compounds)
Kekulé structure (for aromatic compounds)
leaving group
leaving group
leaving group
leaving group
lignans
lignans
meso
-compound
molecular rearrangement
molecular rearrangement
molecular rearrangement
molecular rearrangement
molecular rearrangement
NIH
shift
NIH
shift
nitrilium ions
nitrilium ions
ortho
- and
peri
-fused (polycyclic compounds)
ortho
- and
peri
-fused (polycyclic compounds)
ortho
-fused (polycyclic compounds)
oxocarbons
π-adduct
phenols
photo-Fries rearrangement
photo-Fries rearrangement
phthaleins
planar chirality
polyketides
pseudo-asymmetric carbon atom
pseudo bases
pseudo bases
quinhydrones
Reissert compounds
rhodamine dyes
ring assembly
ring assembly
rotenoids
sulfonphthaleins
tetracyclines
xanthene dyes
parameter
