147611-07-2Relevant academic research and scientific papers
Substituent effects on the solvolysis rates and gas phase stabilities of 1,2,2-trimethyl-1-phenylpropyl and 1,2,2-trimethyl-1-(2-methylphenyl)propyl systems
Nakata, Kazuhide,Fujio, Mizue,Mishima, Masaaki,Nomura, Hideyuki,Tsuno, Yuho,Nishimoto, Kichisuke
, p. 581 - 590 (2007/10/03)
Substituent effects on the solvolysis rates of 1,2,2-trimethyl-1- phenylpropyl chlorides in 80% (v/v) aq acetone at 45 °C and 1,2,2-trimethyl- 1-(2-methylphenyl)propyl p-nitrobenzoates in 50% (v/v) aq ethanol at 75 °C were correlated with the Yukawa-Tsuno
Substituent effect on the solvolysis of α-t-butyl-α-methylbenzyl chlorides
Fujio, Mizue,Nomura, Hideyuki,Nakata, Kazuhide,Saeki, Yoshihiro,Mishima, Masaaki,Kobayashi, Shinjiro,Matsushita, Toshio,Nishomoto, Kichisuke,Tsuno, Yuho
, p. 5005 - 5008 (2007/10/02)
The substituent effect on the solvolysis rates of α-t-butyl-α- methylbenzyl chlorides in 80% aq. acetone was correlated to give p=-4.3 and r=0.91 in terms of the LArSR Eq. (1). This slightly reduced r value relative to full conjugation corresponds to a deviation by 0=24.5° from the coplanarity of the benzylic π-system.
