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 substitution.:
-Cl
-CN
-OH
-OCH3
Withdrawal of electrons through resonance:
-NHCOCH3
-SO3H
-OCOCH3
-NO2
ortho/para-directed substitution:
-NH2
-CN
-OCH3
-SO3H
-F
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....
arrange the following substituents in decreasing order of ring activation for electrophilic aromatic substitution: -NHCOCH3, -CH3, -OCH3, -OH, NO2, -H, Cl, NH2.
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
1. (0.3pts) Identify the most reactive site(s) on the substituted arenes below toward electrophilic aromatic substitution SO, NO2 2. (0.7pts) For each functional group, identify the description that best matches the group's substituent effects. Some of the statements below will require more than one answer to be fully correct. CO" -OH + Br -CH2CH3 collon të na pécon tim a. Donates electrons by hyperconjugation and does not donat lectrons by resonar BO b. Withdraws electrons inductively and withdraw c. Deactivates...