



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 sequence of reactions : 
Molar mass of the product formed (A) is ______ g mol\(^{-1}\).
Predict the major product $ P $ in the following sequence of reactions:
(i) HBr, benzoyl peroxide
(ii) KCN
(iii) Na(Hg), $C_{2}H_{5}OH$
Nature of compounds TeO₂ and TeH₂ is___________ and ______________respectively.
The magnitude of heat exchanged by a system for the given cyclic process ABC (as shown in the figure) is (in SI units):
