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Chemical reaction
Vicinal difunctionalization refers to a chemical reaction involving transformations at two adjacent centers (most commonly carbons). This transformation
Vicinal_difunctionalization
Molecular-structure relationship
2-relationship). It may arise from vicinal difunctionalization. For example, the molecule 2,3-dibromobutane carries two vicinal bromine atoms and 1,3-dibromobutane
Vicinal_(chemistry)
Class of organic compounds
intermediate carbocation. Less aggressive reagents suffice for vicinal difunctionalization. In industry, the diol ethylene glycol forms when ethylene oxide
Alcohol_(chemistry)
Organic reaction
keto-enol tautomerism to the saturated carbonyl compound. In vicinal difunctionalization the proton is replaced by another electrophile. In conjugate
Nucleophilic conjugate addition
Nucleophilic_conjugate_addition
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VICINAL DIFUNCTIONALIZATION
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VICINAL DIFUNCTIONALIZATION
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