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Explain the mechanism of S_(N^(1)) and S_(N^(2)) reactions with examples.
The correct decreasing order of reactivity for a given (R) group in both S_(N^(1)) " and " S_(N^(2)) reaction mechanism is :
Out of S_(N^(1)) and S_(N^(2)) reaction, which is accompanied by inversion of configuration?
(A) Vinyl chloride undergoes S_(N^(1)) " and "S_(N^(2)) reactions. (R) Allyl carbocations is stabilised due to resonance.
Identify number of substrate those can give S_(N^(1))" and "S_(N^(2)) reaction both .
Consider the following statements : (1)Brideherated halides are inert towards both S_(N^(1)) and S_(N^(2)) reaction till one of the ring size is eoght member ring ) (2) The first step in both S_(N^(1)) and E_(1) reactions is the same (3) S_(N^(2)) reactions proceed with total retention of configuration (4) E_(2) elimination s are by the use of a solvent of low polarity and high concentration of a stromng base Which of the above statements are correct?
