Abstract
1. From the IR spectra of the O-methyl(phenyl)methylchlorophosphonates it follows that the stabilization of one conformer is characteristic for these compounds. 2. Employing the method of dipole moments, it was determined that this confirmation can be either the form with a cis-position of the P=O and O-CH3 bonds, or with a gauche-position (the projection of OC is located between PO and PCl). 3. An estimate of the interactions of the unbound atoms disclosed that the latter conformation is more favorable.
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