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A H2O-promoted and (NH4)2CO3-enabled deiodoamination and defluoroiminization reaction of fluoroalkyl alkenes has been developed under transition-metal-free conditions. Structurally important fluoroalkylated 1,5-diazapentadienes were obtained in excellent Z-selectivity with good functional group tolerance. The versatility of the method was illustrated in the synthesis of valuable organofluorides from the obtained products. Compared to traditional synthetic methods, several apparent limitations, including distillation for purification, multistep manipulation, harsh reaction conditions, moisture exclusion, and the use of toxic/sensitive reagents, could be avoided. The key to the success of the reaction is the use of (NH4)2CO3 as a commercially available, inexpensive, low-toxic, and efficient NH2/NH source and water as a C(sp3)–F bond cleavage promoter. Moreover, the distinctive fluorine effects of perfluoroalkyl substituents on substrates are also vital for enhancing the reaction efficiency. [ABSTRACT FROM AUTHOR]