The stability of free radicals mirrors that of carbocations. Similar to carbocations, tertiary radicals exhibit greater stability compared to secondary and primary radicals. This phenomenon can be elucidated by the electron-donating (+I) effect of alkyl groups bonded to carbon radicals. As the number of alkyl groups attached to the carbon radical increases, there is a corresponding rise in the availability of electrons, leading to enhanced stabilization. Consequently, tertiary free radicals are more stabilized than secondary and primary counterparts.
The overall stability order among free radicals is:
triphenyl methyl > benzyl > allyl \(> 3^{\circ} > 2^{\circ} >1^{\circ} >\) methyl > vinyl.
So, the correct option is (C): III
List-I | List-II | ||
(A) | 1 mol of H2O to O2 | (I) | 3F |
(B) | 1 mol of MnO-4 to Mn2+ | (II) | 2F |
(C) | 1.5 mol of Ca from molten CaCl2 | (III) | 1F |
(D) | 1 mol of FeO to Fe2O3 | (IV) | 5F |
List-I | List-II | ||
(A) | [Co(NH3)5(NO2)]Cl2 | (I) | Solvate isomerism |
(B) | [Co(NH3)5(SO4)]Br | (II) | Linkage isomerism |
(C) | [Co(NH3)6] [Cr(CN)6] | (III) | Ionization isomerism |
(D) | [Co(H2O)6]Cl3 | (IV) | Coordination isomerism |
Organic Chemistry is a subset of chemistry dealing with compounds of carbon. Therefore, we can say that Organic chemistry is the chemistry of carbon compounds and is 200-225 years old. Carbon forms bond with itself to form long chains of hydrocarbons, e.g.CH4, methane and CH3-CH3 ethane. Carbon has the ability to form carbon-carbon bonds quite elaborately. Polymers like polyethylene is a linear chain where hundreds of CH2 are linked together.
Read Also: Organic Compounds
Organic chemistry is applicable in a variety of areas including-