Question

The stability of carbocation is both influenced by both resonance and inductive effect, an alkyl group has an electron releasing inductive effect, an alkyl group attached to the positively charged carbon of a carbo cation tends to release charge on the carbon stability decreases as + decreases the groups which exerts - effect like CI,F. NO2 are decreases the stability of carbocation. Which of the following is correct about the species: (CH3)3 - C* Option A a) It is planar Option B b) Its Ct is sp2 hybridised Optionc c) A nucleophile can attack on its C+ Option D d) All of these​

Answer 1

Answer:

Explanation:

effect like CI,F. NO2 are decreases the stability of carbocation. Which of the following is correct about the species: (CH3)3 - C* Option A a) It is planar Option B b) Its Ct is sp2 hybridised Optionc c) A nucleophile can attack on its C+ Option D d) All of these​