Electrochemical CH bond functionalization of organic molecules has emerged as one of the most powerful tools for the synthesis of carbon–carbon and carbon–heteroatom bonds. In past decades, metal‐catalyzed CH activation has attracted significant attention owing to the drawbacks of the conventional methods. At the same time, classical approaches suffer from serious limitations such as the use of expensive catalytic systems, toxic reagents, harsh reaction conditions, and additional waste generation. This has highlighted the need for a sustainable and atom‐efficient solution in the form of various modern‐day techniques. Metal‐ and oxidant‐free electrochemical CH functionalization has proved to be an efficient alternative in terms of efficacy as well as atom economy. Herein, we have discussed about the contribution of metal‐free oxidative electrochemical CH activation in the construction of challenging CC and C–heteroatom (CN, CO, CS, C–halogen) bonds. Detailed mechanistic descriptions and applications toward synthesis of bio‐active drug molecules are also considered till April 2021.