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Haloalkanes and haloarenes are classified based on the number of halogen atoms present, exhibiting distinct chemical properties and reactivity. Their synthesis is primarily achieved through various methods such as nucleophilic substitution and electrophilic aromatic substitution, with significant applications across industries. Understanding their behavior and reactivity is crucial, particularly in terms of environmental impact and organic synthesis.
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Term: Nucleophilic substitution
Definition: A reaction mechanism where a nucleophile replaces a leaving group in a haloalkane.
Term: Elimination reaction
Definition: A process in which a b-hydrogen and a halogen are removed from adjacent carbon atoms, forming an alkene.
Term: Ambident nucleophiles
Definition: Nucleophiles that can react through two different atoms, each providing a site for nucleophilic attack.
Term: Chirality
Definition: A property of a molecule that has a non-superimposable mirror image, often leading to optical activity.