How does the intermediate produced in nucleophilic aromatic substitution differ from the intermediate produced in electrophilic aromatic substitution? How are the two intermediates similar? Briefly explain.

sorry i was late, but i don't know what assignment your talking about, i'm in flvs as well, im in earth space science. but u are behind pace bc every class should be in the 3's or 4'

because natural gas is colorless, odorless, and tasteless, distributors add mercaptan (a chemical that smells like sulfur) to give natural gas a distinct unpleasant odor (it smells like rotten eggs). they locate the types of rock that are likely to contain natural gas deposits.

c is having 4 valence electrons and is bonded to three hydrogens and one sulphur atom, therefore, the number of bond pair is equal to four. as all the valence electrons are used in forming the bonds so, there is no lone pair left on carbon.

s is having 6 valence electrons and is bonded to one other sulfur atom and one carbon atom, therefore, the number of bond pair is equal to 2. as only two valence electrons are used in forming the bonds so, four electrons are left. therefore, two lone pairs are present on s.