Answer:
Then, at some point, these higher energy electrons give up their "extra" energy in the form of a photon of light, and fall back down to their original energy level.
Explanation:
When properly stimulated, electrons in these materials move from a lower level of energy up to a higher level of energy and occupy a different orbital.
Answer:
carbon with graphite as the allotrope
Explanation:
Equiv means equivalent ...
a) Group 2 elements have 2 electrons on their outer shell, so they form a 2+ charge.
b) they lose 2 electrons as they are transferred to the non metal.
c)They obtain this charge as when they are made into an ionic compound the 2 electrons on the outer shell are transferred to the non metal, meaning there are 2 more protons that electrons, giving it a positive charge.
hope this helps! :)
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>