| Name of Reagent | Conditions | Example of its Use |
| K2Cr2O7 with conc. H2SO4 | Warm gently | Oxidising agent, used commonly for oxidising secondary alcohols to ketones. |
| Excess conc. H2SO4 | heat to 170 C | Dehydrating agent, used to dehydrate alcohols to alkenes. |
| Cl2(g) | Ultra Violet light | Free radical reaction, used to convert alkanes to haloalkanes. |
| Br2 in CCl4 | Room temperature, in the dark | Electrophilic addition, converts alkenes to dihaloalkanes. |
| H2(g) | Nickel catalyst, 300 C and 30 atmospheres pressure | Hydrogenating agent, used to convert benzene to cylcohexane. |
| H2(g) | Nickel catalyst, 150 C | Reducing agent, used to convert alkenes to alkanes |
| Tin in hydrochloric acid | Reflux | Reducing agent for converting nitrobenzene to phenylamine. |
| Acidified KMNO4 | Room temperature | Oxidising agent, converts alkenes to diols. |
| NaOH in ethanol | Reflux | Elimination reaction, converts haloalkanes to alkenes. |
| Aqueous NaOH | Reflux | Nucleophilic substitution, converts haloalkanes to alcohols. |
| Mg in dry ether | Reflux | Used to make grignard reagents with haloalkanes. |
| PCl5 | Room temperature | Chlorinating agent, reacts with OH group in alcohols and carboxyllic acids |
| HNO3 and H2SO4 | 55 C | Adds NO2 group onto benzene ring. |
| Cl2 and AlCl3 | Warm gently | Adds Cl group onto benzene ring. |
| CH3CH2Cl and AlCl3 | Warm gently | Adds CH3CH2 group onto benzene ring. |
| HCl and NaNO2 | Below 5 C | Forms diazonium salts with phenylamine.
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