anthocyanin HO MOH lt; gt; HOW 0 – `OH Ha The reaction above

in /by

anthocyanin HO MOH lt; gt; HOW 0 – `OH Ha The reaction above

Multiple choices questions:

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anthocyaninHOMOH < > HOW0 -`OHHaThe reaction above is reactant favored . Which of the below energetic arguments best justifies this data ?2) CH ; CH , OH is a less stable , stronger acid , than the acid on the product side because it has possible resonance structures as aconjugate base , which delocalizes the electrons , lowering the PE due to less electronicelectron repulsions .b ) CH ; CH , OH] is a less stable , weaker acid , than the acid on the product side because no possible resonance structures exist as aconjugate base . Where anthocyanin does resonance as a conjugate base , making it the stronger acid.C ) Resonance for the base on the reactant side creates more organization of the water molecules , decreasing the entropy of thesystem more so than with the base on the product side .$) Resonance for the base on the reactant side creates less organization of the water molecules , decreasing the entropy of thesystem less than with the base on the product side*

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