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In the disubstitution reaction of 3-methyl-2-butanol with 1,4-dimethoxybenzene, the formation of the new carbon-carbon bonds could result in three isomers around the benzene ring. What are the roles of o,m,p-directing effects and steric effects that cause only one isomer to be formed in the reaction?
In the disubstitution reaction of 3-methyl-2-butanol with 1,4-dimethoxybenzene, the formation of the new carbon-carbon bonds could result in three isomers around the benzene ring. What are the roles of o,m,p-directing effects and steric effects that cause only one isomer to be formed in the reaction?
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