The radical stability trend

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[andrewjustin]

2:14 Hi, would you please elucidate why the likewise is not true for allylic and benzyl cations? The positive charge can also resonate with the pi bond so shouldn't the carbocation's stability be identical to the radical's stability?

[bwavely]

About the carbocation trend, I don't quite agree that the tertiary carbocation is more stable than a benzylic/allylic carbocation, and between the benzylic and allylic carbocation, I'd say the benzylic carbocation is more stable because of much resonance...but please get back to me about this.

[itzcassiieex]

okay....kind of annoyed he doesn't post the answer to see if I got it right

[nitinpatil]

Please explain, why there is such opposit stability orders between tertiary & allylic carbocation & radicals?

[ehsan]

a (least stable) < d < c < b (most stable)
Is that correct?

[emperor]

Can you please tell me why vinylic radical are less stable or unstable please help me out....

[jessicatucker]

Wish I would have seen this BEFORE my exam. Thank you for explaining it in a SIMPLE way!

[uptempo]

I got.... (most stable) b > (second most stable) c > (third most stable) a > (least stable) d

[innocentmukora]

I think there is an error benzylic carbocations are more stable the the standard tertiary carbocations

[imtiasbakar]

thankyou but I have little doubt about one thing how tertiary carbo cations are more stable than benzylic and allylic carbocations . I thought benzylic and allylic carbocations are more stable due to resonance effect

[mujiii]

I thought it is useful but sadly no. Where the hell are the answers?

[quantised]

Can you provide the solution to the last problem??.. because I have a major test in 2 days

[yangsi]

Woooow You are actually very good Thanks Cute Sir