Chemistry, 30.07.2021 02:10 bobelliot67789
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
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In an energy pyramid, which level has the most available energy?
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1)each group 16 element has how many valence electrons? ( )4 ( )6 ( )8 ( )16 2)how many dots appear in the dot structure for calcium ion, ca2+? ( )zero ( )one ( )two ( )eight 3) which of the following atoms forms a cation to obtain an octet of outer shell electrons? ( )magnesium ( )oxygen ( )fluorine ( )helium 4) an al3+ ion contains 13 protons and 10 electrons. ( )true ( )false 5) valence and non-valence electrons are represented in lewis dot structures. ( )true ( )false
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How do cfcs cause ozone depletion? how do cfcs cause ozone depletion? ultraviolet radiation breaks down cfcs, molecules containing chlorine. chlorine then breaks one oxygen atom away from ozone, leaving behind a paired oxygen molecule. ultraviolet radiation breaks down cfcs, molecules containing chlorine. chlorine then breaks two oxygen atoms away from ozone, leaving behind a paired oxygen molecule. ultraviolet radiation creates cfcs, molecules containing chlorine. chlorine then breaks two oxygen atoms away from ozone, leaving behind a paired oxygen molecule. ultraviolet radiation creates cfcs, molecules containing chlorine. chlorine then breaks one oxygen atom away from ozone, leaving behind a paired oxygen molecule.
Answers: 2
During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Gr...
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