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In the following carbocation, $\mathrm{H} / \mathrm{CH}_3$ that is most likely to migrate to the positively charged carbon is

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$\mathrm{H}$ at $\mathrm{C}-2$
$\mathrm{H}$ at $\mathrm{C}-2$
Hydride shift from $\mathrm{C}-2$ will give most stable resonance stabilised carbocation as Fig.
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