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Concepts and reason

This problem is based on the bimolecular nucleophilic substitution SN2{{\rm{S}}_{\rm{N}}}2 mechanism of alkyl halide.

The SN2{{\rm{S}}_{\rm{N}}}2 mechanism involves the inversion of configuration as the attack of nucleophile on sp3 hybridized carbon of alkyl halide and removal of leaving group occurs simultaneously in a single step.

Fundamentals

In a SN2{{\rm{S}}_{\rm{N}}}2 mechanism, the reaction proceeds through a five-membered transition stage, which has partial attachment of nucleophile (Nu-) and partial detachment of leaving group X-.

The reaction is given below:

H
NHZ +
UH
+
TH
NH2
H

The mechanism is given below:

H ||LIULIH-
一人一个,
---x
--NH2
Hlli U11
T
+
CNH.
HH
HNH

Ans:

Structures of products of the reaction are given below:

NH2
H

The selection for nucleophile, substrate and leaving group is given below:

)
CH,I is the substrate, NH, is the nucleophile and I is the leaving group.
NH, is the substrate, CH,I is the nucleophile and

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For the following SN2 reaction, draw the organic and inorganic products of the reaction, and identify...
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