Table 2.
Simple oxidized molecules
| Compound, pKa | kCl•, mol–1 dm3 s–1 | Method, pH | Reference |
|---|---|---|---|
| Methanol | 1.0 ± 0.2×109 | LFP, 6 | Buxton et al. 2000 |
| 1.0 ± 0.1×109 | LFP, 5.4 | Wicktor et al. 2003 | |
| 9.0×109 | LFP, 7 | Lei et al. 2019 | |
| Ethanol | 2.25×109 | Compl., ESR, 2 | Gilbert et al. 1988 |
| 1.7 ± 0.3×109 | LFP, 6 | Buxton et al. 2000 | |
| 2.2 ± 0.3×109 | LFP, 5.4 | Wicktor et al. 2003 | |
| 1-Propanol | 2.2 ± 0.4×109 | LFP, 5.4 | Wicktor et al. 2003 |
| 2-Propanol | 6×109 | PR | Mertens and von Sonntag 1995 |
| 1.5 ± 0.2×109 | LFP, 6 | Buxton et al. 2000 | |
| 3.2 ± 0.7×109 | LFP, 5.4 | Wicktor et al. 2003 | |
| 2-Butanol | 5.0 ± 0.6×109 | LFP, 5.4 | Wicktor et al. 2003 |
| tert-Butanol | 2.2×109 | Compl., ESR, 2 | Gilbert et al. 1988 |
| 3×108 | PR | Mertens and von Sonntag 1995 | |
| 3.2×108 | LFP, 6, 5 °C | Buxton et al. 2000 | |
| 4.78×108 | LFP, 6, 15 °C | ||
| 6.2 ± 0.3×108 | LFP, 6, 25 °C | ||
| 8.51×108 | LFP, 6, 35 °C | ||
| 1.5 ± 0.1×109 | LFP, 5.4 | Wicktor et al. 2003 | |
| Formaldehyde (hydrated) | 1.4 ± 0.1×109 | PR, 6 | Buxton et al. 2000 |
| 1.4 ± 0.3×109 | LFP, 5.4 | Wicktor et al. 2003 | |
| Acetaldehyde | 6.3 ± 0.4×108 | LFP, 6 | Buxton et al. 2000 |
| Acetone | < 5×106 | LFP, 6 | Buxton et al. 2000 |
| 7.8 ± 0.7×107 | LFP, 5.4 | Wicktor et al. 2003 | |
| 2-Butanone | 2.4 ± 0.3×108 | LFP, 5.4 | Wicktor et al. 2003 |
| Formic acid, 3.75 | 1.3 ± 0.1×108 | LFP, 1 | Buxton et al. 2000 |
| 2.8 ± 0.3×109 | LFP, 1 | Wicktor et al. 2003 | |
| Formate | 4.2 ± 0.1×109 | LFP, 6 | Buxton et al. 2000 |
| Acetic acid, 4.75 | 2×108 | Compl., ESR, 2 | Gilbert et al. 1988 |
| 3.2 ± 0.2×107 | LFP, 1 | Buxton et al. 2000 | |
| 1.0 ± 0.2×108 | LFP, 1 | Wicktor et al. 2003 | |
| Acetate | 3.7 ± 0.4×109 | PR, 6 | Buxton et al. 2000 |
| Propionic acid, 4.88 | 8×108 | Compl., ESR, 2 | Gilbert et al. 1988 |
| 1.2 ± 0.3×109 | LFP, 1 | Wicktor et al. 2003 | |
| Isobutyric acid, 4.86 | 1.7 ± 0.3×109 | LFP, 1 | Wicktor et al. 2003 |
| Diethyl ether | 1.3 ± 0.1×109 | LFP, 5.8 | Wicktor et al. 2003 |
| Methyl-tert-butyl ether | 1.3 ± 0.1×109 | LFP, 5.4 | Wicktor et al. 2003 |
| Methyl formate | 2.0 ± 0.1×107 | LFP, 4 | Buxton et al. 2001 |
| Ethyl formate | 7.2 ± 0.2×107 | LFP, 4 | Buxton et al. 2001 |
| Methyl acetate | 1.4 ± 0.1×107 | LFP, 4 | Buxton et al. 2001 |
| Ethyl acetate | 8.0 ± 0.7×107 | LFP, 4 | Buxton et al. 2001 |
| Acetylacetone, 8.9 | 2.9 ± 0.3×109 | Comp., 7 | Lei et al. 2019 |
| Fumaric acid, 3.03, 4.44 | 3~3×109 | Compl., ESR, 2 | Gilbert et al. 1988 |
| β-Cyclocitral | 9.58 ± 0.38 × 109 | Comp, 7 | Xiang et al. 2020 |
| 1,4-Dioxan | 2.8–3.4×109 | Est | Li et al. 2017 |
| 4.38 ± 0.38×106 | PR, 5.8 | Patton et al. 2017 | |
| Tetrahydrofuran | 2.6 ± 0.4×109 | LFP, 5.4 | Wicktor et al. 2003 |