Physics
Scientific paper
Nov 1964
adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=1964natur.204..876g&link_type=abstract
Nature, Volume 204, Issue 4961, pp. 876 (1964).
Physics
1
Scientific paper
THE remarkable prevalence of re-arrangement in simple alkyl groups during the formation of alkyl halides, and the concomitant loss in optical purity have been loosely ascribed to the intermediate formation of a carbonium cation1. The conversion of an alkyl halide into the alcohol, ester, or ether must therefore be scrutinized for points of correlation. There are few published examples of alkyl rearrangement in the solvolysis of straight chain alkyl halides. Isopropanol was formed in the mercury catalysed solvolysis of n-propyl bromide in aqueous formic acid, and the carbonium ion mechanism was postulated2.
Gerrard W.
Hudson H. R.
No associations
LandOfFree
Carbonium Ion Mechanism and Results of Solvolysis of (+)-2-Bromo-octane does not yet have a rating. At this time, there are no reviews or comments for this scientific paper.
If you have personal experience with Carbonium Ion Mechanism and Results of Solvolysis of (+)-2-Bromo-octane, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Carbonium Ion Mechanism and Results of Solvolysis of (+)-2-Bromo-octane will most certainly appreciate the feedback.
Profile ID: LFWR-SCP-O-1342864