Question

Which of the following compounds undergoes nucleophilic
substitution reaction most easily ?

Answer 1

Answer:

alhyl halide is the write answer I think

Answer 2

Paranitrochlorobenzene has the most affinity towards nucleophilic substitution.

Explanation:

• Paranitrochlorobenzene has a nitro group in the para position of the chlorobenzene.

• The nitro group has two oxygen group with the nitrogen itself.

• All the three atoms of the nitro group are very much electronegative.

• So they draws huge pool of electron from the benzene ring.

• This in turn draws the electron from chlorine.

• So the carbocation formation of the molecule becomes more easy with Paranitrochlorobenzene.

• So it forms nucleophilic substitution more easily.

For more information about nucleophilic substitution,

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Explain why alkyl halides show nucleophilic substitution reaction

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Ch3f ch3cl ch3br ch3i increasing reactivity towards nucleophilic substitution and increasing order of dipole moment