Which of the following is most reactive towar | vedclass

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(B) The reactivity of carbonyl compounds towards nucleophilic addition depends on two main factors: $1$. Steric hindrance: Smaller groups around the c

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Cyclohexa$-2,5-$diene$-1,4-$dione

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(B) The reactivity of carbonyl compounds towards nucleophilic addition depends on two main factors: $1$. Steric hindrance: Smaller groups around the carbonyl carbon increase reactivity. $2$. Electronic effects: Electron-withdrawing groups increase the electrophilicity of the carbonyl carbon,thereby increasing reactivity. Among the given options,$Cyclohexa-2,5-diene-1,4-dione$ (also known as $p-benzoquinone$) has two carbonyl groups and is conjugated with double bonds. The presence of two electron-withdrawing carbonyl groups and the conjugated system makes the carbonyl carbon highly electrophilic,making it the most reactive towards nucleophilic addition.

Which of the following is most reactive towards nucleophilic addition reaction?

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