The correct sequence of bond enthalpy of ‘C–X’ bond is
CH3−Cl > CH3−F > CH3−Br > CH3−I
CH3−F < CH3−Cl < CH3−Br < CH3−I
CH3−F > CH3−Cl > CH3−Br > CH3−I
CH3−F < CH3−Cl > CH3−Br > CH3−I
To determine the correct sequence of bond enthalpy for the ‘C–X’ bond in methyl halides, we must understand the concept of bond enthalpy, which is the measure of bond strength in a chemical bond.
Bond Enthalpy Explanation: Bond enthalpy is the energy required to break one mole of bonds in gaseous molecules. A higher bond enthalpy indicates a stronger bond. The bond enthalpy of a C–X bond decreases as we move down the halogen group (F, Cl, Br, I) due to increased atomic size and decreased electronegativity.
Comparison of C–X Bonds:
From this understanding, the correct sequence of bond enthalpies is:
CH_3-F > CH_3-Cl > CH_3-Br > CH_3-I
Conclusion: The correct answer is CH3−F > CH3−Cl > CH3−Br > CH3−I because bond strength decreases as the size of the halogen increases. This trend matches the provided option and confirms our understanding of bond enthalpies in methyl halides.

A sphere of radius R is cut from a larger solid sphere of radius 2R as shown in the figure. The ratio of the moment of inertia of the smaller sphere to that of the rest part of the sphere about the Y-axis is : 
A constant voltage of 50 V is maintained between the points A and B of the circuit shown in the figure. The current through the branch CD of the circuit is :
The current passing through the battery in the given circuit, is: 
Given below are two statements:
Statement I: The primary source of energy in an ecosystem is solar energy.
Statement II: The rate of production of organic matter during photosynthesis in an ecosystem is called net primary productivity (NPP).
In light of the above statements, choose the most appropriate answer from the options given below:
‘Alkyl halide’ is the very common name for haloalkanes. The written format for haloalkane in the IUPAC name is “numerical position-alphabetically placed halo- root-word-ane”
‘Aryl Halide’ is the very common name for haloarenes. In the nomenclature system, the numerical prefixes are named, depending on the basic position of the halogen atom in the aromatic ring.
In presence of more than one halogen atom, the halogen group is named and the aromatic ring is numbered based on the numerical position of the aromatic ring. Numerical prefixes are written in the format (1, 2) ; (1,3) ; (1,4). Always the least number is given to the halogen number.
Read More: Nomenclature of Haloalkanes and Haloarenes

Nomenclature of Haloalkanes and Haloarenes