78072-78-3Relevant academic research and scientific papers
Substituent Effects in the Solvolysis of p-(2-Substituted Cyclopropyl)-α-Methylbenzyl Chlorides
Kusuyama, Yoshiaki,Kubo, Takako,Iyo, Masami,Kagosaku, Tamami,Tokami, Kenjiro
, p. 2954 - 2960 (2007/10/02)
The solvolysis rates of p-(cis- or trans-2-substituted cyclopropyl)-α-methylbenzyl chlorides including electron-donating and electron-attracting substituents relative to a hydrogen substituent were measured in 80percent aqueous acetone.The trans isomers w
ELECTRON-DONATING CHARACTERISTICS OF HALOGENOCYCLOPROPYL GROUPS. KINETICS OF THE SOLVOLYSIS OF SUBSTITUTED 2-PHENYL-2-CHLOROPROPANES
Kulinkovich, O. G.,Tishchenko, I. G.,Reznikov, I. V.,Pap, A. A.
, p. 396 - 400 (2007/10/02)
The kinetics of the solvolysis of stereoisomeric 2--2-chloropropanes and 2--2-chloropropanes (X = Cl, Br) in 90percent aqueous acetone were investigated, and the ?+ constants of the halo
