# How to decide the order of stability of allylic carbocations when comparing to benzylic carbocation?

I was going through my organic notes and found this order of stability of carbocation:

3° benzylic > 2° benzylic > 2° allylic > 3° alkyl

I understand that all this is explained on the basis of combined result of resonance and inductive effect. What if one has to predict these?

For example, if I ask you where will you place 3° allylic and where will you place $$\ce{Ph-(CH+)-C=R}?$$ How to decide the order in these cases if this kind of question comes up in an exam?

• Combining electronic effects of inductive as well as mesomeric type. As you said. – Alchimista Feb 15 at 10:14
• @Alchimista Thanks for the comment 1st of all secondly,where will we place the given compound in the order that I have mensioned? – Veerain Feb 16 at 8:11