Question

explain the electrophilic addition to 1,3 butadiene.​

Answer 1

Answer:

Mechanism for the Electrophilic Addition to Conjugate Dienes

For 1,3-butadiene, the proton is added to form the allylic, resonance stabilized carbocation intermediate. The resulting cation has a substantial delocalization energy, with the charge distributed over two carbons.

Answer 2

$\huge\bigstar\mathtt{ \color{red}{A} \color{orange}{N} \color{yellow}{S} \color{lightgreen}{W} \color{blue}{E} \color{indigo}{R}\bigstar}$

Mechanism for the Electrophilic Addition to Conjugate Dienes

Mechanism for the Electrophilic Addition to Conjugate DienesFor 1,3-butadiene, the proton is added to form the allylic, resonance stabilized carbocation intermediate. The resulting cation has a substantial delocalization energy, with the charge distributed over two carbons

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