To determine which of the given carbocations is the most stable, we need to analyze each option based on the degree of substitution of the carbocation and the factors affecting their stability.

This is because tertiary carbocations have three alkyl groups that can donate electron density through hyperconjugation and inductive effects, making them more stable. Therefore, the most stable …

Therefore, based on this concept, we can say that the carbocation in option 3) is more stable as the electrons can move freely in this molecule. So, the correct answer is “Option C”.

Jan 19, 2020 · Hyper conjugation provides stability to carbocation. It is proportional to number of alpha hydrogen (adjacent H). 4th option has max (5) alpha hydrogen, so it will be most stable.

A tertiary carbocation is the most stable carbocation due to the electron releasing effect of three methyl groups. An increased + I effect by three methyl groups stabilizes the positive charge on the carbocation.

Jan 7, 2025 · To determine the most stable carbocation, we need to consider the degree of substitution of the carbocation. More substituted carbocations are generally more stable due to hyperconjugation …

In CH+ 3, the vacant p-orbital is perpendicular to the plane in which C-H bonds lie and hence there is no possibility of overlapping. Thus CH+ 3 lacks hyperconjugation stability and is the least stable …

Jan 3, 2025 · Carbocation stability is determined by the number of alkyl groups attached to the positively charged carbon atom. More alkyl groups lead to greater stability due to inductive effects and …

Jan 28, 2018 · The stability of carbocation is 3°-carbocation > 2°-carbocation > 1°-carbocation (a) (CH3)3C---CH2+ {1°-carbocation} (b) (CH)3C+ {3°-carbocation} (c)CH3-CH2-CH2+ {1°-carbocation} …

Therefore, (C H 3) 3 C + is the most stable carbocation. Note: Carefully classify the given carbocations into 1 o, 2 o and 3 o to determine the stability. Greater the dispersal of positive charge more is the …