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>
Answer:
The number of valence electrons can be known from the group that the element is in (except the lanthanides, actinides and groups 3-12).
Explanation:
Group 1 has 1 valence electron. Group 2 has 2 valence electrons. Group 13 has 3 valence electrons. Group 14 has 4, group 15 has 5, group 16 has 6, group 17 has 7, and group 18 has 8.
Group 18 are the noble gases which are stable.
Group 17 are the halogens and react well with the alkali metals.
"X" in the reaction above is acetic acid with a chemical formula CH3COOH. The chemical reaction would be NaOH + CH3COOH = NaCH3COO + H2O. This is a neutralization reaction in which it produces a salt and water. The salt produced is called sodium acetate.
Answer:
5.85 g C2H6O has more carbon
Explanation:
Weight of carbon in 4.71 g of C6H12O6
grams
Weight of carbon in 5.85 g of C2H6O
grams
Hence, 5.85 g C2H6O has more carbon
