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Nope. There are a few (literally, you can count them on fingers of one hand) that would be less stable. The absolute majority of the allylic carbocations are more stable than tertiary.
@VictortheOrganicChemistryTutor sir I am confused everywhere in internet it is saying that ter. Carbocation is more stable than allylic ones. Please guide me
@@SaurabhSharma-p2k There are quite a few people on the internet that will also argue that the Earth is flat. Paying attention to what you read and the context is important. The allyl carbocation (CH2=CH-CH2+) is less stable than a 3⁰ carbocation. This is *NOT* the same as allylic carbocation, which is R-CH=CH-CH(+)-R. Allylic carbocations are more stable than tertiary.
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Hey Victor you are an amazing teacher. You put in a lot of effort with the examples and explain really well! I am definitely subscribing!
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10:58 This product's name is 2,5-Dimethylhexa-2,4-diene not hexa-3,4-diene
Good catch! Thank you for noticing!
@@VictortheOrganicChemistryTutor Sir, I have a question. Would you like to help me?
@@VictortheOrganicChemistryTutor Why the alpha hydrogens in the butan-2-one are less acidic than alpha hydrogens in butanal ?
Aldehydes are more polarized so they act as a stronger electron-withdrawing group making the alpha position more acidic.
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No need to go to extremes, but donations are always appreciated 😜
But tertiary carbonation is more stable than allylic carbonation n??
Nope. There are a few (literally, you can count them on fingers of one hand) that would be less stable. The absolute majority of the allylic carbocations are more stable than tertiary.
@VictortheOrganicChemistryTutor sir I am confused everywhere in internet it is saying that ter. Carbocation is more stable than allylic ones. Please guide me
@@SaurabhSharma-p2k There are quite a few people on the internet that will also argue that the Earth is flat.
Paying attention to what you read and the context is important.
The allyl carbocation (CH2=CH-CH2+) is less stable than a 3⁰ carbocation. This is *NOT* the same as allylic carbocation, which is R-CH=CH-CH(+)-R. Allylic carbocations are more stable than tertiary.
@@VictortheOrganicChemistryTutor thank you sir for your time and effort
Understood the context