✦ LIBER ✦

Rates of Solvolysis of the m- and p-Phenyl-, m- and p-Methylthio-, and m- and p- Trimethylsilylphenyldimethylcarbinyl Chlorides. Steric Inhibition of Resonance as a Factor in Electrophilic Substituent Constants1,2

✍ Scribed by Brown, Herbert C.; Okamoto, Y.; Inukai, T.

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Spectral comparison of steric inhibition

✍ Twine, Charles E.; Bursey, Maurice M. 📂 Article 📅 1974 🏛 American Chemical Society 🌐 English ⚖ 888 KB

Through-bond transmission of substituent

✍ Adcock, William; Krstic, Alexander R.; Duggan, Peter J.; Shiner, V. J.; Coope, J 📂 Article 📅 1990 🏛 American Chemical Society 🌐 English ⚖ 956 KB

Unusually high exo:endo rate ratios in t

✍ Brown, Herbert C.; Takeuchi, Kenichi. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 338 KB

Effect of a homoallylic double bond on t

✍ Peters, Edward N.; Brown, Herbert C. 📂 Article 📅 1972 🏛 American Chemical Society 🌐 English ⚖ 254 KB

Energies, E1, M1, and E2 transition rate

✍ P. Jönsson; P. Rynkun; G. Gaigalas 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 357 KB

Remote and proximate substituent effects

✍ Coates, Robert M.; Fretz, E. Robert 📂 Article 📅 1977 🏛 American Chemical Society 🌐 English ⚖ 393 KB