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Give the order of stability of these carbocations

Give the order of stability of the given carbocations.

Usually stability is determined by studying effects taking place in the carbocation. All are resonating and there is no diff in inductive effect.So I want to know how the molecular weight might affect stability

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    $\begingroup$ Give us your thoughts on this or the question will be closed $\endgroup$ – Waylander Jan 21 at 18:36
  • $\begingroup$ Usually stability is determined by studying effects taking place in the carbocation. All are resonating and there is no diff in inductive effect.So I want to know how the molecular weight might affect stability $\endgroup$ – hp2505 Jan 22 at 15:24
  • $\begingroup$ Edit your question to include this comment $\endgroup$ – Waylander Jan 22 at 15:36
  • $\begingroup$ Ok i did it...now its a valid question right? $\endgroup$ – hp2505 Jan 23 at 17:02
  • $\begingroup$ I think so, I have voted to reopen $\endgroup$ – Waylander Jan 23 at 17:31
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The question is pretty easy though the INDUCTIVE and MESOMARIC effects are same but there is a diffrence in the HYPERCONJUGATIVE Effect as in HYPERCONJUGATIVE Effect the bond between $C-H$ breaks to provide stability thus any change in bond energy of the bond to be broken changes the strength of effect.

Now as the bond strength of $C-T$ bond if highest hence the HYPERCONJUGATIVE Effect of $\ce{CT3}$ decreases and hence the carbocation is least stable.And $\ce{CH3}$ is most stable

You can read more about Hyperconjugation in the following Site: https://chemistry.tutorvista.com/inorganic-chemistry/hyperconjugation.html

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