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Combustion: This is the most common reaction, where a hydrocarbon reacts with oxygen to produce carbon dioxide, water, and heat. This is a highly exothermic process, forming the basis of energy production in internal combustion engines and fuels like methane, propane, and butane. Substitution: Common in saturated hydrocarbons (alkanes), this reaction involves replacing one or more hydrogen atoms with a different atom or group, such as a halogen (chlorine or bromine). This process, often requiring heat or light to begin, converts alkanes into haloalkanes, which are crucial for chemical synthesis. Addition: Specific to unsaturated hydrocarbons (alkenes and alkynes), this reaction breaks the double or triple bonds between carbon atoms to allow new atoms or molecules to join the carbon chain. An example is hydrogenation, where hydrogen is added to an alkene to create an alkane. Cracking: A process used in the petrochemical industry to break down large, heavy hydrocarbon molecules into smaller, more useful ones. Reforming: This process converts alkanes into alkenes and aromatic hydrocarbons, altering the molecular structure to improve fuel quality. Key Characteristics Hydrocarbons are generally nonpolar and relatively unreactive at room temperature. They require specific conditions, such as high temperatures, catalysts, or exposure to light (like ultraviolet light for halogenation), to react. Combustion always produces carbon dioxide and water when sufficient oxygen is present #neet2026 #jeemains #jeemain #jeemains2026 #neet #neetmumbra #hydrocarbon #oneshotrevision #organicchemistry #organicbooster #kolbe #wurtzreaction #halogenation #electrophilic #substitution #bestrevision #oneshot #masteringorganicreagents #reagents #neetmotivation #conceptneetdigital #conceptmumbra #mumbra #mumbrakausa #bestlecture