Name the following benzene derivatives using ortho, meta, and para to identify the relative position of substituents.
(a)

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Name the following benzene derivatives using ortho, meta, and para to identify the relative position of substituents.
(a)
The zwitterionic form of carbonyls is often used to explain their electrophilicity. Draw the zwitterionic structure of NO+2. Why is this such a great electrophile at the central nitrogen?
Predict the product of the following Friedel–Crafts alkylation reactions. Assume only one alkyl group adds in each case.
(d)
Predict the product of the following Friedel–Crafts acylation reactions.
(b)
In Section 23.7.4, we learned that Friedel–Crafts alkylation suffers from overalkylation.
(a) Draw the product of a Friedel–Crafts reaction that resulted in three methyl groups adding to the ring.
(b) Why is hard to stop at the addition of one alkyl group?
Convert the given name into the corresponding IUPAC name.
(b)