Answer:
The order of reactivity towards electrophilic susbtitution is shown below:
a. anisole > ethylbenzene>benzene>chlorobenzene>nitrobenzene
b. p-cresol>p-xylene>toluene>benzene
c.Phenol>propylbenzene>benzene>benzoic acid
d.p-chloromethylbenzene>p-methylnitrobenzene> 2-chloro-1-methyl-4-nitrobenzene> 1-methyl-2,4-dinitrobenzene
Explanation:
Electron donating groups favor the electrophilic substitution reactions at ortho and para positions of the benzene ring.
For example: -OH, -OCH3, -NH2, Alkyl groups favor electrophilic aromatic substitution in benzene.
The -I (negative inductive effect) groups, electron-withdrawing groups deactivate the benzene ring towards electrophilic aromatic substitution.
Examples: -NO2, -SO3H, halide groups, Carboxylic acid groups, carbonyl gropus.
The "Van Gogh" one is subjective, because it expresses opinion and is not a true, hard fact. :)
There is no picture hunny. Please add a picture please boo.
Answer: AgCl + Fe
Explanation:
A single replacement reaction is one in which a more reactive element displaces a less reactive element from its salt solution. Thus one element should be different from another element.
A general single displacement reaction can be represented as :
The blanced chemical reaction will be :
Ethanol is polar because the oxygen atoms attract electrons because of their higher electronegativity than other atoms in the molecule. Thus the -OH group in ethanol has a slight negative charge. Ammonia (NH3) is polar. Sulfur dioxide (SO2) is polar.
