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@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.inductive
m
INDUCTIVE
why inductive?
BOND LENGTH iguess
James Ashenhurst
Master Organic Chemistry
3 Factors That Stabilize Carbocations
Three main factors increase the stability of carbocations: Increasing the number of adjacent carbon atoms (methyl < primary < secondary < tertiary (most stable) Adjacent pi bonds that allow the carbocation p-orbital to be part of a conjugated pi-system system ("delocalization through resonance") Adjacent atoms with lone pairs More details below.
iteachchem
Transcription requested by Opt
Hey, you're asking about question seven, right? So generally, what difference would it make if you have a hydrogen versus a deuterium versus a tritium? Is it the inductive effect or the hyperconjugation effect? Which one, which one would get affected?
It's hyperconjugation that gets affected.
Hyperconjugation would be stronger
Think of it this way. Is it easier for a C-H bond to break or a C-D bond?
C-H
because of size order of H,D,T is T>D>H
So the greater ease of hyperconjugation is in which system?
C-H?
@Opt ?
Yup, that should be it.
+solved @Opt + @iTeachChem
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