Chloral hydrate gives one apparently diffusion-controlled wave (E~/~. ~bout --1.4 v vs. S.C.E.), dichloroacetaldehyde two kinetic-controlled waves (--1.0 and --1.7 v), and chloroacetaldehyde two kinetic-controlled waves (--1.1 and -1.7 v). The chloral hydrate wave is actually controlled by a composite of diffusion and kinetic processes. Coulometric and polarographic data show that chloral hydrate is reduced to dichloroacetaldehyde hydrate; the latter dehydrates, and the unhydrated molecule is reduced to chloroacetaldehyde, which is then reduced to acetaldehyde; finally, the latter is reduced to ethyl alcohol or 2,3-dihydro• or both. This over-all reduction process forms only one wave; the acetaldehyde, whose reduction should result in a second wave, is formed in such a small amount that the wave is clearly demarcated in ammonia buffers only. Dichloroacetaldehyde is reduced to chloroacetaldehyde, which in turn is reduced to acetaldehyde with the formation of one wave; acetaldehyde reduction accounts for the second wave. Chloroaceta]dehyde's first wave is due to reduction to acetaldehyde; the second due to reduction of acetaldehyde.