



Step 1. Understanding Vinyl Halide: Vinyl halides are compounds in which a halogen atom is directly attached to an sp2 hybridized aliphatic carbon atom, which forms part of a double bond.
Step 2. Examine Each Structure: Option (1): Contains a halogen attached to an sp2 hybridized carbon in a double-bonded system, classifying it as a vinyl halide. Option (2): Represents an allyl halide, with the halogen attached to an sp3 hybridized carbon adjacent to a double bond. Options (3) and (4): Both structures are aryl halides, with the halogen attached to an aromatic ring.
Step 3. Conclusion: Option (1) is the correct example of a vinyl halide.
A vinylic halide is an organic compound where a halogen atom is directly bonded to a carbon-carbon double bond. This is different from allylic halides, where the halogen is bonded to a carbon adjacent to the double bond.
Let's examine the options to identify the vinylic halide:
Based on the analysis, the correct answer is Option 1, where we see the halogen directly bonded to the carbon-carbon double bond, confirming it as a vinylic halide.





Consider the following reaction of benzene. the percentage of oxygen is _______ %. (Nearest integer) 
Two p-n junction diodes \(D_1\) and \(D_2\) are connected as shown in the figure. \(A\) and \(B\) are input signals and \(C\) is the output. The given circuit will function as a _______. 
A substance 'X' (1.5 g) dissolved in 150 g of a solvent 'Y' (molar mass = 300 g mol$^{-1}$) led to an elevation of the boiling point by 0.5 K. The relative lowering in the vapour pressure of the solvent 'Y' is $____________ \(\times 10^{-2}\). (nearest integer)
[Given : $K_{b}$ of the solvent = 5.0 K kg mol$^{-1}$]
Assume the solution to be dilute and no association or dissociation of X takes place in solution.