Although chlorine is an electron withdrawing group, yet it is ortho-, para- directing in electrophilic aromatic substitution reactions. Why?

Althrough chlorine is an electron withdrawing group, yet it is ortho-para-directing in electrophilic aromatic substitution reactions. Explain why it is so ?

For an electrophilic aromatic substitution reaction

(i). Why are alkyl halides insoluble in water. ? (ii). Although chlorine is an electron withdrawing group, yet it is ortho and para directing in electrophilic aromatic substitution.

Introduction OF Electrophilic Aromatic Substitution Reaction

Which of the following is not a meta-directing group in electrophilic aromatic substitution?

Halogens are deactivating yet ortho,para directing in electrophilic aromatic substitution. Which statements do not explain this ?

For a typical nucleophilic aromatic substitution reaction to take place . 1. Nucleophilic atom should be of oxygen nitrogen or sulphur. 2. Leaving groups should be halide. 3. There should be strong electron withdrawing at ortho and para position to leaving group. Fastest nucleophilic aromatic substitution reaction take place in :

Which of the following stes of groups activates the ortho and para positions in electrophilic aromatic substitutions ?

For a typical nucleophilic aromatic subsitution reaction to take place. (1) Nucleophilic atom should be of oxygen, nitrogen or sulphur. (2) Leaving group should be halide . (3) There should be strong electron withdarwing at ortho and para position to leaving group. Fastest nucleophilic aromatic substitution reaction take place in :