The question is incomplete, the complete question is shown in the image attached
Answer:
A and B
Explanation:
The electrophilic substitution of arenes yields a cation intermediate. The positive charge of the cation is delocalized over the entire ring.
The -CN group directs incoming electrophiles to the ortho/para position. The resonance structures for the chlorination of benzonitrile are shown in the question.
Recall that -CN is an electron withdrawing group. The resonance forms that destablize the carbocation intermediate are those in which the -CN group is directly attached to the carbon atom bearing the positive charge as in structures A and B.
Maybe her old shoes had soft worn out bottoms and she slips in them. So her new shoes had more grip than her old ones so they kept her from falling.
Answer:
its easy ask to chrome or search in yt ;)
ionic bond is formed between ca and cl forming molecule cacl2 ca has 2 velancy and cl has one velancy (ca has 2 electrons in its outer most shell while cl has 1 electron vecancy in its outermost shell). So ca would make bond with 2 cl atoms
The Coriolis Effect describes the turn of the wind to the right in the Northern Hemisphere caused by earth's rotation.