The major products of the following reaction | vedclass

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(B) The reaction shown is the final step of the haloform reaction. In this step,the hydroxide ion $(OH^{-})$ acts as a nucleophile and attacks the car

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$PhCOO^{-}$ and $CHBr_{3}$

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(B) The reaction shown is the final step of the haloform reaction. In this step,the hydroxide ion $(OH^{-})$ acts as a nucleophile and attacks the carbonyl carbon of the $PhCOCBr_{3}$ molecule. This leads to the formation of a tetrahedral intermediate,which then collapses to expel the stable $CBr_{3}^{-}$ carbanion and form benzoic acid $(PhCOOH)$. Finally,an intermolecular proton exchange occurs between the carboxylic acid $(PhCOOH)$ and the $CBr_{3}^{-}$ carbanion,resulting in the formation of the benzoate ion $(PhCOO^{-})$ and bromoform $(CHBr_{3})$.

The major products of the following reaction are:

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The major product obtained in the following reaction is:

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