1.) NAOH : Elimination reaction. Converts haloalkanes to alkenes.
2.) Acidified KMnO₄ : Oxidizing agent. Converts alkenes to diols.
3.) Tin in HCL : Reducing agent. Converts Nitro benzene to phenyl amine.
4.) H₂₍g₎, Nickel, 300°C and 30atm pressure : Hydrogenation. Converts Benzene to Cylcohexane.
5.) H₂₍g₎, Nickel, 150°C : Reducing agent. Converts Alkenes to Alkanes.
6.) Br in CCl₄ : Electrophilic addition. Converts Alkenes to dihaloalkanes.
7.) SOCl₂, Sunlight : Radical reaction. Converts Alkenes to Haloalkanes.
8.) Excess Conc. H₂SO₄ : Dehydrating agent. Dehydrates Alcohol to Alkenes.
9.) K₂Cr₂O₇ with Conc. H₂SO₄ : Oxidizing agent. Oxidizing secondary Alcohols to Ketones