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.
Lithium has the lowest. if fluorine is the highest then lithium is the lowest. i hope this helps you out!
Answer:
2-Methylpentane is a branched-chain alkane with the molecular formula C6H14. It is a structural isomer of hexane composed of a methyl group bonded to the second carbon atom in a pentane chain.
<span>The answer is 4. The molecules of each material entice each other over dispersion (London) intermolecular forces. Whether a substance is a solid, liquid, or gas hinge on the stability between the kinetic energies of the molecules and their intermolecular magnetisms. In fluorine, the electrons are firmly apprehended to the nuclei. The electrons have slight accidental to stroll to one side of the molecule, so the London dispersion powers are comparatively weak. As we go from fluorine to iodine, the electrons are far from the nuclei so the electron exhausts can more effortlessly misrepresent. The London dispersion forces developed to be increasingly stronger.</span>
Solid (ice caps)
Liquid (oceans, rivers, lakes, etc)
Gas (clouds)
