which carbon cation is most stabilized
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A tertiary Carbocation is more stable than primary and secondary ones, although “stability” is a relative term (carbocations are very reactive, transient species); this is due to the electron-releasing effect of its substituent Alkyl groups.
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Alkyl groups – methyl, ethyl, and the like – are weak electron donating groups, and thus stabilize nearby carbocations. What this means is that, in general, more substituted carbocations are more stable: a tert-butyl carbocation, for example, is more stable than an isopropyl carbocation
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