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
The reaction sequence given below is carried out with 16 moles of X. The yield of the major product in each step is given below the product in parentheses. The amount (in grams) of S produced is ____. 
Use: Atomic mass (in amu): H = 1, C = 12, O = 16, Br = 80

In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by:
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-