EFFECTS OF ALKYL GROUPS IN NUCLEOPHILIC SUBSTITUTION

[1] Mechanism of substitution at a saturated carbon atom Part XVI Hydrolysis of methyl, ethyl, isopropyl and tert -butyl bromides in acidic solutions under conditions believed to be conducive to uniformity of mechanism [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1940, : 945 - 948

[2] NUCLEOPHILIC DISPLACEMENT IN THE BENZENE SERIES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (06) : 1574 - 1579

[3] BERLINER E, COMMUNICATION

[4] Mechanism of substitution at a saturated carbon atom Part XVII Polar effects in alkyl groups, as illustrated by solvolytic substitutions of p-alkylbenzhydryl chlorides [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1940, : 949 - 956

[5] Mechanism and kinetics of substitution at a saturated carbon atom. [J]. TRANSACTIONS OF THE FARADAY SOCIETY, 1941, 37 : 0603 - 0631

[1] Mechanism of substitution at a saturated carbon atom Part XVI Hydrolysis of methyl, ethyl, isopropyl and tert -butyl bromides in acidic solutions under conditions believed to be conducive to uniformity of mechanism [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1940, : 945 - 948

[2] NUCLEOPHILIC DISPLACEMENT IN THE BENZENE SERIES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (06) : 1574 - 1579

[3] BERLINER E, COMMUNICATION

[4] Mechanism of substitution at a saturated carbon atom Part XVII Polar effects in alkyl groups, as illustrated by solvolytic substitutions of p-alkylbenzhydryl chlorides [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1940, : 949 - 956

[5] Mechanism and kinetics of substitution at a saturated carbon atom. [J]. TRANSACTIONS OF THE FARADAY SOCIETY, 1941, 37 : 0603 - 0631