A mechanism that may lead to asymmetry between the concentrations of levo and dextro enantiomers is suggested. Under certain conditions, chiral symmetry breaking is possible due to the cooperative effect in solution when the chiral configuration of a molecule is affected by the chirality of others. This effect may lead to a kind of "phase transition" of the system to the state where a presence of only one type of enantiomers, either levo or dextro, is energetically advantageous. Cooperativity results from an increase of the effective radius of the intermolecular interaction due to mobility of molecules in the liquid and gas phases. The kinetics of the reactions, as well as possible ways to the synthesis of the compounds with desirable chirality, are considered. An experiment on chiral symmetry breaking in sodium chlorate crystallization, an example of chiral symmetry breaking in a macro system, is discussed.