MECHANISM OF SUBSTITUTION AT A SATURATED CARBON ATOM .27. THE ROLE OF STERIC HINDRANCE - (SECTION-B) A COMPARISON OF THE RATES OF REACTION OF ETHYL AND NEOPENTYL BROMIDES WITH INORGANIC IODIDES IN ACETONE SOLUTION

被引：15
作者：
DOSTROVSKY, I
HUGHES, ED
机构：
来源：
JOURNAL OF THE CHEMICAL SOCIETY | 1946年 / MAR期
关键词：
D O I：
10.1039/jr9460000161
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
引用
收藏
页码：161 / 164
页数：4
相关论文
共 11 条
[1]   An acetylenic analog of neopentyl bromide, evidence that the hindrance to displacement reactions in neopentyl halides is steric in nature [J].
Bartlett, PD ;
Rosen, LJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1942, 64 :543-546
[2]   The relation between the structure of organic halides and the speeds of their reaction with inorganic iodides. II. A study of the alkyl chlorides [J].
Conant, JB ;
Hussey, RE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1925, 47 :476-488
[3]  
CONANT JB, 1924, J AM CHEM SOC, V46, P245
[4]  
HAMMETT, 1940, PHYSICAL ORGANIC CHE, P154
[5]  
HUGHES, 1935, J CHEM SOC, P1525
[6]  
HUGHES, 1935, J CHEM SOC, P244
[7]  
LANG, 1922, Z ANORG CHEM, V122, P332
[8]  
LANG, 1925, Z ANORG CHEM, V144, P75
[9]  
LANG, 1925, Z ANORG ALLG CHEM, V142, P279
[10]   A new jodometric method, which is based on the formation and measurement of iodine cyanide II. [J].
Lang, R .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1925, 142 (3/4) :229-256
12