explanation
Type 1- All groups having a lone pair at the key atom are ortho, para-directing groups. For example, -X, -O-, -OH, -OR, -OCO-R, -NH2, -NHR, -NHCOR etc.
Type 2- All groups having their key atom multiply bonded to more powerful element are meta--directing groups. For example, -NO2, -CN, -COOH, -COR,-SO3H etc.
Type 3- Alkyl groups are ortho, para-directing groups. whereas -CX3,-(NR3)+ are meta--directing groups.
The directive influence can easily be decided by drawing the resonating structures of the intermediate after ortho, meta or para - attack and comparing their stabilities.
Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution reactions. Substituents can...
Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution reactions. Substituents can activate or deactivate the ring to substitution, donate or withdraw electrons inductively, donate or withdraw electrons through resonance, and direct substitution either to the ortho/para or to the meta positions. From the following lists, select the substituents that have the indicated property. The substituents are written as -XY, where X is the atom directly bound to the aromatic ring. Activation of the ring towards...
Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution reactions. Substituents can activate or deactivate the ring to substitution, donate or withdraw electrons inductively, donate or withdraw electrons through resonance, and direct substitution either to the ortho/para or to the meta positions. From the following lists, select the substituents that have the indicated property. The substituents are written as XY, where X is the atom directly bound to the aromatic ring. Activation of the ring towards...
Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution reactions. Substituents can activate or deactivate the ring to substitution donate or withdraw electrons through resonance, and direct substitution either to the ortho/para or to the meta positions. From the following lists, select the substituents that have the indicated property. The substituents are written as -XY, where X is the atom directly bound to the aromatic ring. Activation of the ring towards substitution. Withdrawal of electrons through...
Substituents on an aromatic ring can have several effects on
electrophilic aromatic substitution reactions. Substituents can
activate or deactivate the ring to substitution, donate or withdraw
electrons inductively, donate or withdraw electrons through
resonance, and direct substitution either to the ortho/para or to
the meta positions. From the following lists, select the
substituents that have the indicated property. The substituents are
written as -XY, where X is the atom directly bound to the aromatic
ring.
Substituents on an aromatic ring...
Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution reactions. Substituents can activate or deactivate the ring to substitution, donate or withdraw electrons inductively, donate or withdraw electrons through resonance, and direct substitution either to the ortho/para or to the meta positions. From the following lists, select the substituents that have the indicated property. The substituents are written as -XY, where X is the atom directly bound to the aromatic ring.
Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution reactions. Substituents can activate or deactivate the ring to substitution, donate or withdraw electrons inductively, donate or withdraw electrons through resonance, and direct substitution either to the ortho/para or to the meta positions. From the following lists, select the substituents that have the indicated property. The substituents are written as -XY, where X is the atom directly bound to the aromatic ring.
Synthesis of disubstituted benzenes involves two steps, each introducing one of the functional groups For the synthesis of p-chlorosulfonic acid, select the reagent for each step and draw the structure of the monosubstituted intermediate compound. Put the intermediate substituent in the same place that it is oberved in the product (i.e. either the top or the bottom of the benzene ring). Intermediate Step 1 Step 2 O C2, peroxide O Ch. FeCl3 O SOs, H2S04 O Cl2. peroxide O Cl2....
In an electrophilic aromatic substitution reaction, which group is both ortho, para directing and ring deactivating? of Select one: O -NH2 O-SO3H O-1 0 -CN O-OCH3
Please help... Need a detail Mechanism of this reaction.
Thanks...
Electrophilic aromatic substitution describes the reaction where a hydrogen from a benzene ring is replaced by an electrophile. Halogenation, nitration, sulfonation, alkylation and acylation are all possible using this type of reaction. The electrophile attacks the pi electrons of the aromatic ring, yielding a benzenonium ion. The substituted aromatic product is obtained when a proton is lost, restoring the aromatic system. If there is a substituent on the aromatic ring...
arrange the following substituents in decreasing order of ring activation for electrophilic aromatic substitution: -NHCOCH3, -CH3, -OCH3, -OH, NO2, -H, Cl, NH2.