<span>Lithium has a property
of high reactivity and to obtain lithium is through electrolysis of its fused
salts. Because lithium is very reactive, it is not found free so electrolysis
is use to split it apart to get it. Moreover,
Lithium is an alkali metal with single valence electron that is easily given up
to form cation, which make it a good conductor of heat and electricity.</span>
<span> </span>
Answer:
3–methyl–2–butanol
Explanation:
To name the compound, we must:
1. Identify the functional group.
2. Give the functional group of the compound the lowest possible count.
3. Locate the longest continuous carbon chain. This gives the parent name of the compound.
4. Identify the substituent group attached.
5. Give the substituent group the lowest possible count.
6. Combine the above to get the name of the compound.
Now, let us obtain the name of the compound.
1. The functional group of the compound is Alcohol i.e —OH.
2. The functional group is located at carbon 2.
3. The longest continuous carbon chain is carbon 4 i.e butane. But the presence of the functional group i.e OH will replace the –e in butane with –ol. Therefore, the compound is butanol.
4. The substituent group attached is methyl i.e CH3.
5. The substituent group is located at carbon 3.
6. Therefore, the name of the compound is:
3–methyl–2–butanol.
Answer:
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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>
