stability of carbocations depends on

'Stability of carbocations depends upon the electron releasing inductive effect of groups adjacent to positively charged atom involvement of neighbouring groups in hyperconjugation and resonace''. Write structure of various carbocations that can be obtained from 2-methylbutane. Arrange these carbocations in order of increasing stability

'Stability of carbocations depends upon the electron releasing inductive effect of groups adjacent to positively charged atom involvement of neighbouring groups in hyperconjugation and resonace''. Which of the following ions is more stable ? Use resonance of explain your answer.

'Stability of carbocations depends upon the electron releasing inductive effect of groups adjacent to positively charged atom involvement of neighbouring groups in hyperconjugation and resonace''. The structure of triphenylmethyl cation is given below. This is very stable and some of its salts can be stored for months. Explain the cause of high stability of this cation

'Stability of carbocations depends upon the electron releasing inductive effect of groups adjacent to positively charged atom involvement of neighbouring groups in hyperconjugation and resonace''. Draw the possible resonance structures for CH_(3) - underset(..)overset(..)(O) - overset(+)(C) H_(2) and predict which of the structures is more stable. Give reason for your answer.

Assertion (A) : SN^(1) reaction is carried out in the presence of a plar protic solvent. Reason (R): A polar protic solvent increases the stability of carbocation due to solvation.

Assertion: The order of stability of carbocations is 3^(@) gt 2^(@) gt 1^(@) Reason: Carbon atom in carbocation is in sp^(3) state of hybridisation.

Arrange stability of given carbocations in decreasing order

Stability of ecosystem depends upon

"Stability of a community depends on its species richness." Write how did David Tilman show this experimentally.