The given compound is:
To identify the type of compound, let’s examine its structure. The compound shown contains a halogen (Cl) attached to a carbon that is adjacent to a double bond (C=C). This arrangement is indicative of an allylic position. The key feature in this structure is that the halogen is bonded to a carbon that is adjacent to a carbon-carbon double bond. This structure defines an allylic halide.
Allylic halides are compounds where a halogen (usually chlorine, bromine, or iodine) is attached to a carbon that is adjacent to a carbon-carbon double bond. The position of the halogen relative to the double bond makes the carbon-halogen bond weaker, which makes these compounds reactive in nucleophilic substitution reactions. \[ \text{Allylic Halide:} \quad \text{R-CH}_2\text{CH=CH}_2\text{Cl} \] The halogen in an allylic halide can be replaced by other nucleophiles in a reaction, making these compounds useful intermediates in organic synthesis.
Based on the structure and the position of the halogen relative to the double bond, we conclude that the given compound is an example of an **Allylic Halide**.
The given compound is an example of Allylic Halide.
A bob of heavy mass \(m\) is suspended by a light string of length \(l\). The bob is given a horizontal velocity \(v_0\) as shown in figure. If the string gets slack at some point P making an angle \( \theta \) from the horizontal, the ratio of the speed \(v\) of the bob at point P to its initial speed \(v_0\) is :
The hydrocarbons such as Haloalkanes and Haloarenes are the ones, in which one or more hydrogen atoms are replaced with halogen atoms. The main difference between Haloalkanes and Haloarenes is that Haloalkanes are derived from open chained hydrocarbons, also called alkanes, and Haloarenes are derived from aromatic hydrocarbons.