Answer:
The correct answer is A electron on the aniline nitrogen are somehow delocalized to the aromatic ring.
Explanation:
The structure of aniline contain double bonds and lone pair of electron in the nitrogen atom of -NH2 group that is attached to the benzene ring.
The electron pair present in the nitrogen atom of -NH3 group of aniline undergo delocalization with the aromatic ring of benzene resulting in the formation of resonance hybrid that increases the ability of nitrogen atom of -NH2 group of aniline to easily donate that lone pair of electron.
ON the other hand the resonance stabilization cannot be possible with the cyclohexylamine ring as it is saturated.
A chemist has discovered<span> a </span>drug<span> that </span>blocks phosphoglucoisomerase<span>, an </span>enzyme<span> that </span>catalyzes<span> the</span>second reaction<span> in </span>glycolysis<span>. </span>He wants<span> to </span>use<span> the </span>drug<span> to </span>treat people<span> with </span>bacterial infections.However<span>, </span>he can't do<span> this </span>because _____<span>. human cells also perform </span>glycolysis<span>; the </span>drug<span> might also poison them. Most NADH ...</span>
There 3 elements wich is
C =4
H=8
O=4
So the total atoms are 16
