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Why is anisole ortho and para director towards electrophile substitution reaction?
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Anisole does not form peroxide easily why?
Oygen atom is strongly bonded to the benzene ring. so, anisole can not easily form peroxides. But diethyl ethers easily form peroxides in air.
What product form when anisole react with HI?
Phenol, though additional iodide salt is sometimes needed.
Why phenol is more reactive than anisol?
Because the -OH group present in phenol is more ring activating than -OCH3 group in anisole.
Why does the friedel crafts acylation of anisole favor the para-methoxyacetophenone?
Anisole has a methoxyl group that participates in activating the benzene ring during acylation. When the benzene ring breaks its bond in order to attach an acetone functional group, it is destablized and therefore energy unfavorable. However, other functional groups like alkoxides (-OR) animo (-NR2), thio groups (-SR) all have lone electrons AND single bonds, which can form into double bonds--donating those electrons to the benzene ring and stabilizing its positive charge. The attachment will always para to the activating group due to steric effects, followed by ortho position due to specific locations that the positive charge can exist (when the methoxyl group adds its electrons).
Give a simple procedure to convert anisole into phenol?
in the presence of con.h2so4 anisole will convert into phenol and hi
Why doesn't Anisole form peroxide easily?
anisole does not form peroxides easily as the oxygen atom is strongly bonded to the benzene ring .
What is an anisole?
An anisole is a type of aromatic compound that has a methoxy group (-OCH3) attached to a benzene ring. It is often used as a solvent in various chemical reactions and as a starting material for the synthesis of other compounds. Anisole has a sweet, pleasant odor and is a colorless liquid at room temperature.
What is the atomic number for Anisole?
Anisole is a compound, not an element and so it does not have an atomic number. It is composed of carbon, hydrogen, and oxygen which have the atomic numbers 6,1, and 8 respectively.
Anisole does not form peroxide easily why?
Oygen atom is strongly bonded to the benzene ring. so, anisole can not easily form peroxides. But diethyl ethers easily form peroxides in air.
What is an anisyl?
An anisyl is any of three isomeric univalent radicals derived from anisole.
What product form when anisole react with HI?
Phenol, though additional iodide salt is sometimes needed.
Why phenol is more reactive than anisol?
Because the -OH group present in phenol is more ring activating than -OCH3 group in anisole.
What is anasoles use?
Anisole is mainly used for its derivatives for many natural and artificial toiletry uses. Its derivatives are often used in items like perfume, pharmaceuticals, and some insect pheromones.
Name two anti-oxidants which are usually added to fat and oil containing foods to prevent?
prevent rancidity???? if it so then the answer is - 1) BHA {Butylated Hydroxy-Anisole} 2) BHT {Butylated Hydroxy-Toluene} Hope it helped!!!
Why should you limit the fat and salt in your diet?
Fats contains Butyric hydroxy anisole,Monosodium acetate,Butyric hydroxy Toluene which in excess causes increased risks of heart strokes,obesity related problems. about common salt ovedose of this causes bones to melt
Why does the friedel crafts acylation of anisole favor the para-methoxyacetophenone?
Anisole has a methoxyl group that participates in activating the benzene ring during acylation. When the benzene ring breaks its bond in order to attach an acetone functional group, it is destablized and therefore energy unfavorable. However, other functional groups like alkoxides (-OR) animo (-NR2), thio groups (-SR) all have lone electrons AND single bonds, which can form into double bonds--donating those electrons to the benzene ring and stabilizing its positive charge. The attachment will always para to the activating group due to steric effects, followed by ortho position due to specific locations that the positive charge can exist (when the methoxyl group adds its electrons).
