The crystals of both dextro and lævo tartaric acids prove to be pyro-electric, that is, develop electric excitation when slightly heated. The end which exhibits the development of the clinodome develops positive electricity in each case, when the crystal is allowed to cool after warming, so that the two varieties are oppositely pyro-electric, just as they are oppositely optically active. The most convenient method of demonstrating the fact is to dust a little of Kundt’s powder, a mixture of finely powdered red lead and sulphur, through a fine muslin sieve on to the crystal as it cools. The sulphur becomes negatively electrified and the red lead positively by mutual friction of the particles in the sifting, and the sulphur thus attaches itself to the positively electrified part of the crystal and the red lead to the negatively electrified end. This phenomenon of the development by the two varieties of an optically active substance of opposite electrical polarity has since been shown to be a general one. Finally, on mixing concentrated solutions containing equivalent weights of dextro and lævo tartaric acid Pasteur observed that heat was evolved, a sign of chemical combination, and the solution afterwards deposited on cooling crystals of racemic acid. Hence, the only conclusion possible is that racemic acid must be a molecular compound of the two oppositely optically active tartaric acids. It thus partakes of the character of a double salt, analogous to potassium magnesium sulphate for instance. Consequently the crystal structure is one in which alternating molecules of the two acids are uniformly distributed, and the case is actually presented of two oppositely enantiomorphous sets of molecules producing a homogeneous structure.