What is anisole from chapter hydrocarbon ??
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an aromatic hydrocarbons or anisole is a hydrocarbon An aromatic hydrocarbon or arene[1] (or sometimes aryl hydrocarbon)[2] is a hydrocarbon with sigma bonds and a delocalized pi electrons between carbon atoms forming a circle. In contrast, aliphatic hydrocarbons lack this delocalizatio. The term 'aromatic' was assigned before the physical mechanism determining aromaticity was discovered; the term was coined as such simply because many of the compounds have a sweet or pleasant odour. The configuration of six carbon atoms in aromatic compounds is known as a benzene ring, after the simplest possible such hydrocarbon, benzene. Aromatic hydrocarbons can be monocyclic(MAH) or polycyclic (PAH).
Some non-benzene-based compounds called heteroarenes, which follow Hückel's rule (for monocyclic rings: when the number of its π-electrons equals 4n + 2, where n = 0, 1, 2, 3,…), are also called aromatic compounds. In these compounds, at least one carbon atom is replaced by one of the heteroatoms oxygen, nitrogen, or sulfur.
Some non-benzene-based compounds called heteroarenes, which follow Hückel's rule (for monocyclic rings: when the number of its π-electrons equals 4n + 2, where n = 0, 1, 2, 3,…), are also called aromatic compounds. In these compounds, at least one carbon atom is replaced by one of the heteroatoms oxygen, nitrogen, or sulfur.
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Anisole is a flavouring agent Anisole is a precursor to perfumes, insect pheromones, and pharmaceuticals. For example, synthetic anethole is prepared from anisole. Anisole undergoes electrophilic aromatic substitution reaction more quickly than does benzene, which in turn reacts more quickly than nitrobenzene. The methoxy group is an ortho/para directing group, which means that electrophilic substitution preferentially occurs at these three sites. The enhanced nucleophilicity of anisole vs benzene reflects the influence of the methoxy group, which renders the ring more electron-rich. The methoxy group strongly affects the pi cloud of the ring, moreso than the inductive effect of the electronegative oxygen.
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