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Is there any reaction in which the cyclisation of the sidechain to form fused ring with benzene causes the losing of aromatic character(conjugation of double bonds) of benzene? If so what are the factors which eliminate the aromaticity? What about the cyclisation of 5-phenyl-3-methyl pent-1-ene in presence of mineral acid (proton)? Is there any reaction in which the cyclisation of the sidechain to form fused ring with benzene causes the losing of aromatic character(conjugation of double bonds) of benzene? If so what are the factors which eliminate the aromaticity? What about the cyclisation of 5-phenyl-3-methyl pent-1-ene in presence of mineral acid (proton)?
Is there any reaction in which the cyclisation of the sidechain to form fused ring with benzene causes the losing of aromatic character(conjugation of double bonds) of benzene? If so what are the factors which eliminate the aromaticity?
What about the cyclisation of 5-phenyl-3-methyl pent-1-ene in presence of mineral acid (proton)?
Please go through attached imagehttps://www.askiitians.com/iit-jee-chemistry/organic-chemistry/iupac-and-goc/reaction-intermediates/
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