Rank the reactivity of the following alkenes toward acid-catalyzed hydration from most reactive to least reactive. (The alkenes are not in the corect order). The image displays a vertical sequence of four organic molecules ranked by their reactivity. It is arranged from "Most reactive" at the top to "Least reactive" at the bottom. Here is a detailed explanation of each compound:1. **Most reactive:** - The first molecule is 1,2-dichloroethene, featuring a two-carbon chain with double bonds between the carbons and each carbon further bonded to a chlorine atom.2. **Second in reactivity:** - The second structure is an alkene with a branched carbon chain. It shows a double bond joining two central carbon atoms with two alkyl groups extending from these carbons.3. **Third in reactivity:** - The third molecule is another branched alkene. It has a similar structure to the second compound but differs in the placement or type of alkyl groups attached.4. **Least reactive:** - The last molecule is a simple linear alkene. It consists of a straight chain of three carbon atoms with one double bond, indicating the least reactivity among the displayed compounds.The diagram uses a descending arrow from the top to the bottom to clearly show the progression from most to least reactive.

Hydration of alkene in the presence of acid proceeds with the formation of a carbocation intermediate.The alkene that forms the most stable carbocation is most reactive and those that form the least stable carbocation are least reactive. Carbocation stability depends upon- Resonance stability Inductive effect of the attached alkyl group.The order is –