Ammonolysis of Alkyl halides followed by the treatment with NaOH solution can be used to prepare primary, secondary and tertiary amines. The purpose…

The correct order of the rate of reaction of the following reactants with nucleophile by SN1 mechanism is: (Given : Structure I and II are rigid) 

Identify the incorrect statements.  Choose the correct answer from the options given below:

For the following Friedel Craft's alkylation reaction, which of the statements are correct?  A. Major product is n-propyl benzene. B. iso-propyl carbocation intermediate is also generated. C. Multiple substitution is inevitable. D. Introducing electron-donating substituent on benzene will not produce any alkyl benzene. Choose the correct answer from the options given below:

Match the LIST-I with LIST-II <table class="pyq-table"><tbody><tr><th>List-I (Reaction)</th><th>List-II (Mechanism)</th></tr><tr><td>A. Williamson Synthesis</td><td>I. Electrophilic addition</td></tr><tr><td>B. Friedel Craft Reaction</td><td>II. Free radical substitution</td></tr><tr><td>C. Bromination of vinyl benzene</td><td>III. Nucleophilic substitution</td></tr><tr><td>D. Chlorination of toluene in light</td><td>IV. Electrophilic substitution</td></tr></tbody></table> Choose the correct answer from the options given below:

Consider the following reactions sequence  When the product (P) is subjected to Carius analysis using $AgNO_3$, $1.0$ g of the product (P) will produce _______ g of the precipitate of AgBr. (Nearest Integer) (Given: molar mass in g mol$^{-1}$ C : 12, H : 1, O : 16, N : 14, Br : 80, Ag : 108)