During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the
benzene ring, that direct ortho/para further stabilize this intermediate by participating in the resonance delocalization of the positive charge. Assume that the following group is present on a benzene ring at position 1 and that you are brominating the ring at positon 4. Draw the structure of the resonance contributor that shows this group actively participating in the charge delocalization. -----OCH3
Aromatic compounds undergo electrophilic aromatic substitution reactions in which the aromatic ring is maintained.
Substituted benzenes may be more or less reactive towards electrophilic aromatic substitution than benzene depending on the nature of the substituent present in the ring.
Substituents that activate the ring towards electrophilic substitution such as -OCH3 are ortho-para directing.
The major products of the bromination of anisole are p-bromoanisole and o-bromoanisole. The resonance structures leading to these products are shown in the image attached.
Typically, only one element is present, so all atomic radii are the same. -Metallic bonding is not directional. -Nearest neighbor distances tend to be small in order to lower bond energy.
We assume you are converting between grams ZnSO4 and mole. You can view more details on each measurement unit: molecular weight of ZnSO4 or mol This compound is also known as Zinc Sulfate. The SI base unit for amount of substance is the mole. 1 grams ZnSO4 is equal to 0.0061941519772353 mole.
Electrons are transferred from atoms of sodium to atoms of phosophorus. This transfer makes the sodium atoms positive and the phosphorus atoms negative. As a result, the sodium and phosphorus atoms strongly attract each other.
