In physical organic chemistry, the GrunwaldâÂÂWinstein equation is a linear free energy relationship between relative rate constants and the ionizing power of various solvent systems, describing the effect of solvent as nucleophile on different substrates. The equation, which was developed by Ernest Grunwald and Saul Winstein in 1948, could be written
where the and are the solvolysis rate constants for a certain compound in different solvent systems and in the reference solvent, 80% aqueous ethanol, respectively. The parameter is a parameter measuring the sensitivity of the solvolysis rate with respect to , the measure of ionizing power of the solvent.
The Hammett equation (Equation 1) provides the relationship between the substituent on the benzene ring and the ionizing rate constant of the reaction. Hammett used the ionization of benzoic acid as the standard reaction to define a set of substituent parameters ÃÂ<sub>X</sub>, and then to generate the ÃÂ values, which represent ionizing abilities of different substrates. This relationship can be visualized through a Hammett plot.
However, if the solvent of the reaction is changed, but not the structure of the substrate, the rate constant may change too. Following this idea, Grunwald and Winstein plotted the relative rate constant vs. the change of solvent system, and formulated this behavior in the GrunwaldâÂÂWinstein equation. Since the equation has the same pattern as the Hammett equation but captures the change of the solvent system, it is considered as an extension of the Hammett equation.
The substitution reaction of tert-Butyl chloride was chosen as reference reaction. The first step, ionizing step, is the rate determining step, SO stands for the nucleophilic solvent. The reference solvent is 80% Ethanol and 20% water by volume. Both of them can carry out the nucleophilic attack on the carbocation.
The S<sub>N</sub>1 reaction is performed through a stable carbocation intermediate, the more nucleophilic solvent can stabilize the carbocation better, thus the rate constant of the reaction could be larger. Since thereâÂÂs no sharp line between the S<sub>N</sub>1 and S<sub>N</sub>2 reaction, a reaction that goes through S<sub>N</sub>1 mechanism more is preferred to achieve a better linear relationship, hence t-BuCl was chosen.
In equation , stands for the rate constant of t-BuCl reaction in 80% aqueous Ethanol, which is chosen as the reference. The variable stands for the rate constant of the same reaction in a different solvent system, such as ethanol-water, methanol-water, and acetic acid-formic acid. Thus, Y reflects the ionizing power of different nucleophile solvents.
The equation parameter m, called the sensitivity factor of solvolysis, describes the compoundâÂÂs ability to form the carbocation intermediate in given solvent system. It is the slope of the plot of log(k<sub>sol</sub>/k<sub>80%EtOH</sub>) vs Y values. Since the reference reaction has little solvent nucleophilic assistance, the reactions with m equal to 1 or larger than 1 have almost full ionized intermediates. If the compounds are not so sensitive to the ionizing ability of solvent, then the m values are smaller than 1. That is: