Save
Common Aromatic Ring Names
Save
Share
Learn
Content
Leaderboard
Learn
Created by
Taynala
Visit profile
Cards (37)
Benzoic
Acid
ortho-
adjacent carbons
para-
separated by
two
carbons
meta-
separated by
one
carbon
NH2
electron donating group
ortho/para directing
OH
electron donating group
ortho/para directing
OR
electron donating group
ortho
/
para directing
NHCOR
electron donating group
ortho/para directing
CH3
electron donating group
ortho
/
para directing
phenyl
electron donating group
ortho/para directing
F
electron donating group
ortho
/
para directing
Cl
electron donating group
ortho
/
para directing
Br
electron donating group
ortho
/
para directing
I
electron donating group
ortho
/
para directing
HC=O
electron donating group
meta
diracting
O=COR
electron donating group
meta
diracting
O=COH
electron donating group
meta
diracting
O=CR
electron donating group
meta diracting
SO3H
electron donating group
meta diracting
CN
electron donating group
meta diracting
NO2
electron donating group
meta diracting
NR3
electron donating group
meta diracting
pyridine
aromatic
Pyrimidine
aromatic
pyrrole
aromatic
imidazole
aromatic
furan
aromatic
thiophen
aromatic
electron withdrawing produced by E.N. difference
inductive effect
F
, Cl,
Br
, I, NO2, COCH3
electron donating
resonance effect
F
,
Cl
, Br, I,
OH
,
NH2
, OR
electron withdrawing
resonance effect
RCOR,
CN
,
NO2
withdrawing electrons inductively but donating electrons through resonance effect
OH
,
NH2
,
OR
ortho-para directing activators
alkyl groups
(
R's
),
OH
/
OR
,
NH2
,
NHR
,
NR2
,
NHCOR
ortho-para directing deactivator
halogens
meta directing deactivators
all electron withdrawing groups except
halogens
directing effect of R1 and R2 in tri-substituted alkenes
if
reinforce
each other than
additive
effect
if
oppose
each other
stronger activiating group
wins
meta di-substituted reaction
will not add between
two R groups
because of
steric hinderance