# Grunwald–Winstein equation

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In physical organic chemistry, the Grunwald–Winstein 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[1][2]

$\log \frac{k_{x,sol}}{k_{x,80\% EtOH}} = mY$

where the kx, sol and kx, 80% EtOH are the solvolysis rate constants for a certain compound in different solvent systems and in the reference solvent, 80% aqueous ethanol, respectively. The m is a parameter of the compound measuring sensitivity of solvolysis rate to Y, the measure of ionizing power of the solvent.[3]

## Background

Dissociation of substituted benzoic acids.

Hammett equation (Equation 1) provides the relationship between the substituent on the benzene ring and the ionizing rate constant of the reaction. Hammett use the ionization of benzoic acid as the standard reaction to define a set of substituent parameters σX, and then generate the ρ values, which represent ionizing abilities of different substrate, through Hammett Plot.

$\log \frac{k_X}{k_H} = \sigma_X\rho$ (1)

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, a plot of relative rate constant vs. the change of solvent system can be generate through an equation, which is the Grunwald-Winstein Equation. Since it has the same pattern with Hammett equation but dealing with the change of solvent system, we can also consider it as a supplement of Hammett Equation.

## Definition

### Reference compound

SN1 mechanism of substitution reaction

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.[4][5]

The SN1 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 there’s no sharp line between SN1 and SN2 reaction, a reaction goes through SN1 mechanism more is preferred to achieve a better linear relationship, hence t-BuCl was chosen.

### Y values

$\log \frac{k_{t-BuCl, sol}}{k_{t-BuCl, 80\% EtOH}} = Y$ (2)

In equation 2, kt-BuCl, 80% EtOH stands for the rate constant of t-BuCl reaction in 80% aqueous Ethanol, it is a constant. kt-BuCl, sol. stands for the k of the same reaction in different solvent system, such as ethanol-water, methanol-water, and acetic acid-formic acid. Thus Y reflects the ionizing power of different nucleophile solvents.

solvent, %by vol. Y solvent, %by vol. Y solvent, %by vol. Y
EtOH-H2O 25 2.908 30 2.753
100 -2.033 20 3.051 20 3.025
98 -1.681 15 3.189 10 3.279
95 -1.287 10 3.312 AcOH-HCOOH
90 -0.747 5 3.397 100 -1.639
80 0 H2O 3.493 90 -0.929
70 0.595 MeOH-H2O 75 -0.175
60 1.124 100 -1.09 50 0.757
50 1.655 90 -0.301 25 1.466
45 1.924 80 0.381 10 1.862
40 2.196 70 0.961
37.5 2.338 60 1.492
35 2.473 50 1.972
30 2.721 40 2.391

### m values

The equation parameter, sensitivity factor of solvolysis, m describes the compound’s ability to form the carbocation intermediate in certain solvent system. It is the slope of the plot of log(ksol/k80%EtOH) vs Y values. Since the reference reaction has little solvent nucleophilic assistance, the reactions with m equal to 1 or lager than 1 have almost full ionized intermediate. If the compounds are not so sensitive to the ionizing ability of solvent, then the m values are smaller than 1. That is:

1. m ≥ 1, the reactions go through SN1 mechanism.

2. m < 1, the reactions go through the mechanism between SN1 and SN2.