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they cause attack on the aryl ring to occur at positions ortho and para to them, while deactivating. David Duchovny One class of FORM ORDER - NOH substituents -- called ortho-para directors -- favors further substitutions mostly at the adjacent carbon and at the ring-site. Those toluenes, having
strong activating groups pose. the phenoxy group a strong but the methyl group is also. File Format: PDFAdobe Acrobat - View as HTML Thus, these positions become activated towards electrophilic aromatic substitution, and the CH3 group is
an ortho-para director, as we learned in organic. File Format: Microsoft Word - View as HTML I thought Cholrine was considered a halogen. Aren'.
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of benzenethiol are the othopara. Once a substitution has occurred that is no longer true. we'll start by looking at the orhto, para-directors. All of the ortho, para directors
except the. File Format: PDFAdobe Acrobat - View