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.
Answer:
Explanation:
Group one elements are alkali metals. All alkali metal have one valance electron. They loses their one valance electron and from cation with charge of +1.
Charges on group one.
Hydrogen = +1
Lithium = +1
Sodium = +1
Potassium = +1
Rubidium = +1
Cesium = +1
Francium = +1
Group two elements are alkaline earth metals. All alkaline earth metal have two valance electron. They loses their two valance electron and from cation with charge of +2.
Charges on group two.
Beryllium = +2
Magnesium = +2
Calcium = +2
Strontium = +2
Barium= +2
Radium = +2
Group 13 elements are boron family. All elements have three valance electrons. They loses their three valance electron and from cation with charge of +3.
Charges on group 13.
Boron = +3
Aluminium = +3
Gallium = +3
Indium = +3
Thallium= +3
Group 13 elements are also shows +1 charge by losing one valance electron.
Water is a polar solvent. Since, 'Like dissolves like' a polar compound will be most soluble in water whereas a non-polar compound will be the least soluble.
The increasing order of polarity for the given organic compounds is:-
CH3OCH3 < CH3NH2 < CH3CHO < CH3CH2OH
Ether is the least polar and hence least soluble in water.
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