Friedel-Crafts alkylation requires an electrophilic aromatic substrate. Aniline does not undergo Friedel-Crafts alkylation because the amino group (-\(NH_2\)) on the benzene ring strongly activates the ring towards electrophilic attack, leading to significant reactivity and making it difficult to control the reaction. Furthermore, the lone pair of electrons on the nitrogen atom in aniline coordinates with the Lewis acid catalyst (like \(AlCl_3\)),
deactivating the ring and preventing alkylation.
The carbylamine test is positive for primary amines. Aniline is a primary amine and will give a positive test.
The correct order of the rate of reaction of the following reactants with nucleophile by \( \mathrm{S_N1} \) mechanism is:
(Given: Structures I and II are rigid) 
| LIST I | LIST II | ||
|---|---|---|---|
| A | Lyman | I | Near IR |
| B | Balmer | II | Far IR |
| C | Paschen | III | Visible |
| D | p-fund | IV | UV |
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The output (Y) of the given logic implementation is similar to the output of an/a …………. gate.