EASY
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Ionic reactions with organic compounds proceed through:

(A) Homolytic bond cleavage

(B) Heterolytic bond cleavage

(C) Free radical formation

(D) Primary free radical

(E) Secondary free radical

Choose the correct answer from the options given below:

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Important Questions on Organic Chemistry- Some Basic Principles and Techniques

MEDIUM
The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due to 
HARD
A solution of (-)1-chloro-1-phenylethane in toluene racemises slowly in the presence of a small amount of SbCl5, due to the formation of :
MEDIUM
In which of the following compounds, the C-Cl bond ionization shall give most stable carbonium ion?
MEDIUM

C7H5O22hvX2C˙6H5+2CO2

Consider the above reaction and identify the intermediated 'X'