The reaction given below is an example of Firedel craft  alkylation reaction.In number of cases of Friedel – crafts alkylation the final product is found to contain a rearranged alkyl group. Generally with stronger Lewis acid product is rearranged due to enough polariazation of complex while with weak Lewis acid no such effect is observed. Temperature also favoures rearranged product.What is electrophile in give reaction?

What is the correct order of steps in the mechanism for a Friedel-Crafts alkylation (after the initial formation of the reactive electrophile, E+)?Select answer from the options belowProton Transfer: Nucleophilic Attack: Loss of a Leaving GroupNucleophilic Attack: Proton TransferProton Transfer: Nucleophilic AttackProton Transfer: Nucleophilic Attack: Proton Transfer

In the proton transfer step of a Friedel-Crafts alkylation reaction, where does the proton go?Select answer from the options belowTo the sigma complexTo the aluminum trichloride, restoring a proper valence shellTo the ring to restore aromaticityTo form an acid byproduct (HX)Save for LaterSubmit Answer

In the proton transfer step of a Friedel-Crafts alkylation reaction, where does the proton go?Select answer from the options belowTo the aluminum trichloride, restoring a proper valence shellTo form an acid byproduct (HX)To the sigma complexTo the ring to restore aromaticity

In the proton transfer step of a Friedel-Crafts alkylation reaction, where does the proton go?Select answer from the options belowTo the aluminum trichloride, restoring a proper valence shellTo the ring to restore aromaticityTo form an acid byproduct (HX)To the sigma complex

Why is it generally inefficient to use a primary alkyl halide as an electrophile in a Friedel-Crafts alkylation?Select answer from the options belowPrimary alkyl halides do not form a sigma complex after a nucleophilic attack since they connect at the primary carbocation site.The use of a primary alkyl halide in a Friedel-Crafts alkylation reaction violates one of the three standard limitations for Friedel-Crafts alkylation reactions.Primary alkyl halides give primary carbocations which can rearrange beforfe being attacked by the aromatic ring, resulting in a mixture of products.Primary alkyl halides are resonance-stabilized, making them unreactive.