Many electrophilic aromatic halogenations require the presence of an aluminum trihalide as a catalyst. We generally acetylated the amino group as protection. Now, this acetanilide can be brominated at Ortho or para position. An atom that is attached to an aromatic system usually hydrogen is replaced by an electrophile is an organic reaction which is called Electrophilic aromatic substitution. There are what you called important electrophilic aromatic substitutions they are aromatic nitration, aromatic sulfonation, aromatic halogenation and acylation and alkylating Friedel-Crafts reaction. Aromatic bromination is an electrophilic aromatic substitution (EAS) reaction, which will require benzene to act as a nucleophile to acquire an electrophile. Therefore, any directing groups that activate the ring will make it react more quickly with respect to aromatic bromination. Acetanilide is a moderately-activated ring <span>having a decent EWG.</span>
<span>C) The bonds prevent ions from moving throughout the crystal, so a solid ionic compound is a poor conductor is your answer, however, technically speaking the bonds prevent electrons from moving, since the ions are locked in place and don't want their electrons to go.</span>
They have the same amount but if you count the wrist it was more then the leg and ankle.
The pressure of the gas will increase with the temperature as each molecule moves around. think of hot air balloons the way they inflate that big balloon is a flame underneath the gas which increases temperature and pressure.
