Which of the following compounds undergoes ma | vedclass

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(A) The extent of hydration of carbonyl compounds depends on the electrophilicity of the carbonyl carbon and steric hindrance. $1$. Electron-withdrawi

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$CF_3-CO-CF_3$

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(A) The extent of hydration of carbonyl compounds depends on the electrophilicity of the carbonyl carbon and steric hindrance. $1$. Electron-withdrawing groups (like $-F$ or $-Cl$) increase the electrophilicity of the carbonyl carbon by the inductive effect ($-I$ effect),making it more susceptible to nucleophilic attack by water. $2$. The compound $CF_3-CO-CF_3$ (hexafluoroacetone) has two highly electronegative $CF_3$ groups,which exert a strong $-I$ effect,significantly increasing the positive charge on the carbonyl carbon. $3$. Consequently,$CF_3-CO-CF_3$ forms a stable hydrate (gem-diol) most readily compared to the other options. Therefore,the correct option is $A$.

Which of the following compounds undergoes maximum hydration?

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