918314-81-5Relevant articles and documents
The leaving group dependence in the rates of solvolysis of 1,2-diphenylethyl system
Santhosh Kumara,Jayakumarb,Balachandranc
experimental part, p. 783 - 788 (2011/05/05)
1,2-Diphenylethyl chloride undergoes solvolysis by SN1 mechanism in aqueous organic solvents. The α-phenyl group of 1,2-diphenylethyl chloride enters into conjugation with the developing carbocationic centre. The β-phenyl group on the other hand was unable to extend its conjugation via neighbouring group participation due to steric inhibition of resonance in the formation of non-classical carbocation. 1,2-Diphenylethyl chloride thus behaves similar to 1-phenylethyl chloride in its solvolysis pattern. The solvolytic rate studies of chloride and methanesulphonate of 1,2-diphenylethyl alcohol in various aqueous organic solvents show that the dispersion observed in the Winstein- Grunwald plot is not due to a change in leaving group but due to the difference in solvation requirements of aromatic and aliphatic groups. Copyright
