Ingold, Sir Christopher

Sir Christopher Ingold, Structure and Mechanism in Organic Chemistry. 2nd edition, ch. 6. London Bell. 

In the 1920s Sir Christopher Ingold proposed a mechanism for dehydrohalogenation that IS still accepted as the best description of how these reactions occur Some of the mfor matron on which Ingold based his mechanism included these facts... 

The mechanisms by which nucleophilic substitution takes place have been the subject of much study Extensive research by Sir Christopher Ingold and Edward D Hughes and their associates at University College London during the 1930s emphasized kinetic and stereochemical measurements to probe the mechanisms of these reactions... 

Cahn and Sir Christopher Ingold (England) and Vladimir Prelog (Switzerland) in the context of a different aspect of organic stereochemistry they will appear again in Chapter 7. 

The role of nitronium ion in the nitration of benzene was demonstrated by Sir Christopher Ingold—the same person who suggested the n1 and n2 mechanisms of nucleophilic substitution and who collaborated with Cahn and Prelog on the R and S notational system. 

Proposed by Edward D. Hughes and Sir Christopher Ingold (the University College, London) in 1937. 

R. S. Cahn, Sir Christopher Ingold, and V. Prelog, Spezifikation der molekularen Chiralitat. Angew. Chem. 78, 413 447 (1966). 

Shoppee. "Christopher Kelk Ingold," 350, 358, 369 and J. H. S. Green, "Sir Christopher Ingold and the Chemistry Department, University College, London," in J. H. Ridd, ed., Studies on Chemical Structure and Reactivity Presented to Sir Christopher Ingold (London Methuen, 1966) 265274, on 271. 

Sir Christopher K. Ingold, following his investiture at Buckingham Palace in 1958. Courtesy of the Chemistry Department of... 

In the year 1937, Edward Davies Hughes and Sir Christopher Ingold proposed a mechanism for an S 2 reaction. 

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