Arrange the following compounds in the increasing order of their reactivity towards HCN. I. Acetaldehyde II. Acetone III. Methyl-tert-butyl ketone IV. Di-tert-butyl ketone
A
III < II < IV < I
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B
II < I < IV < II
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C
IV < III < II < I
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D
II < IV < I < III
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Solution
The correct option is C IV < III < II < I More electron-withdrawing group favours NA reaction (nucleophilic addition reaction), whereas the electron-donating group decreases reactivity towards NA reaction or reactivity towards HCN.
So, increasing the order of reactivity towards HCN is IV < III < II < I.