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166:"Revised Nomenclature for Radicals, Ions, Radical Ions and Related Species (IUPAC Recommendations 1993) Appendix"
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144:, for this reason, they are commonly generated as intermediaries to activate alcohols. To this end,
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The functionalization to include tolyl groups into compounds is often done by
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is reacted in the presence of a base with the corresponding alcohol.
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27:Class of functional groups derived from toluene
34:Structures of the three isomers of tolyl group
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73:, the change of the relative position of the
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7:
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196:. You can help Knowledge (XXG) by
168:. Queen Mary University of London.
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101:which are commonly found in the
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77:and the R substituent on the
81:can generate three possible
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146:4-toluenesulfonyl chloride
142:nucleophilic substitutions
122:Williamson etherification
54:. They have the general
243:Organic chemistry stubs
109:. They are considered
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128:as reagents, or by
107:chemical compounds
83:structural isomers
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190:organic chemistry
132:reactions. Tolyl
48:functional groups
40:organic chemistry
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138:leaving groups
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198:expanding it
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130:C-C coupling
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44:tolyl groups
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248:Aryl groups
115:hydrophobic
105:of diverse
99:aryl groups
50:related to
237:Categories
152:References
134:sulfonates
103:structure
126:alcohols
117:groups.
111:nonpolar
89:), 1,3 (
56:formula
52:toluene
75:methyl
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87:ortho
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95:para
91:meta
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