Which of the following compound is most reactive in the nucleophilic aromatic substitution reaction with NaOH ?

Question

Which of the following compound is most reactive in the nucleophilic aromatic substitution reaction with NaOH ?

Which of the following compound is most reactive in the nucleophilic aromatic substitution reaction with NaOH ?
A. `p-` nitrofluorobenezene
B. `p-`nitrochlorobenzene
C. `p-`nitrobromobenzene
D. `p-`nitroiodobenzene

Monjur Alahi

4 views

2025-01-04 04:42

1 Answers

Related Questions

Aryl halides are less reactive towards nucleophilic substitution reaction as compared to alyl halides due to

2 Answers 4 Views

Aryl halides are less reactive towards nucleophilic substitution because

2 Answers 4 Views

Assertion: Aryl undergoes nucleophilic substitution with ease Reason The carbon halogen bond in aryl halides has partial double bond character .

2 Answers 4 Views

Which of the following compounds does not undergo nucleophilic substitution reactions ?

2 Answers 4 Views

Assertion : Aromatic aldehydes and formadehyde undergo Cannizzaro reaction Reason : Aromatic aldehydes are almost reactive a formaldehyde.

2 Answers 5 Views

The `NH_(2)` group of aniline acts as a / an ________ in electropilic aromatic substitution .

2 Answers 4 Views

Which one is more reactive in nucleophilic acyl substituion. Why is it so ? `F_(3)C-overset(O)overset(||)(C)-O-C_(2)H_(5) ` or `H_(3)C-overset(O)overs

2 Answers 4 Views

Which of the following compounds give a nucleophilic substitution reaction with phosphorus pentachloride?

2 Answers 4 Views

Towards electrophilic substitution, the most reactive is

2 Answers 5 Views

Amines are less reactive in substitution reactions. Their reactivity is much lesser than alcohols and alkylflourides towards substitution. Protonation

2 Answers 4 Views

Salim Ahmed Kawsar · Accepted Answer · 2023-02-05T15:29:48+06:00

Salim Ahmed Kawsar

Correct Answer - 1
In the nucleophilic aromatic substitution reaction reactivity order is `(ArFgtArClgtArBrgtArI)`.

4 views Answered 2023-02-05 15:29