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Indicate by an arrow the positon(s) where `SE` reaction takes place in the following:
image
j. `Ph - CF_(3)`
k. `Ph - overset(o+)(N) R_(3) } NO_(3)^(o-)`
l. `o,m-` and `p-` Ethoxyacentanilide

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a. image
`Se` reaction takes place at the place indicated by the arrows in the centra ring. Since it is joined to two activating phenyl rings.
b. image
c. image
Same explanation as in (b), `p-` product is major.
d. image
Ring `(A)` bonded to `(underset(..)overset(..)(-O-))` group is activated.
RIng `(B)` bonded to `(underset(O)underset(||)(-C-))` group si deactivated `p-` product is major.
e. image
Ring `(B)` is deactivated by `(-CN)` group. Ring `(A)` is activated by `(-CH_(2) - Ar)` group. `p-` product is less hindered from than `orhtho`, so it is major product.
f. image [same explanation as in `(e)`]
g. image
The `(-COOH)` group is deactivating and `m-` directing, `(-CH_(3))` group is activating, and `o-` and `p-` directing class `I(-CH_(3))` decides orientation.
h. image
The `(-COOH)` group is deactivating and `m-` directing, `(-OH)` is activating, and `o-` and `p-` directing class `I (-OH)` decides orientation.
i. image
No reaction because of two strongly deactivity `(-NO_(2))` groups.
However, the `(-NO_(2))` group si `m-` director, if suitable conditions are employed then `(-NO_(2))` directs at `m-` positon.
j. image
Deacttivting by strong `-I` effect of three `F` atoms and `m-` directing.
k. image
Deactivated by strong `-I` effect fo `overset(o+)(N)R_(3)` and `m-` director.
l. image
image
When both the groups are nearly equal moderate activators and both are `o-` and `p-` directing, then the products of the reaction ortho and para to both are obtained.

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