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- Explain why the reaction in Problem 18.48 proceeds dramatically more slowly under neutral conditions than under either acidic or basic conditions.write a balnced chemical reaction to synthesize this compound via fischer esterificationWe your anver on paper and submit a picture here gir emaitto me ty the end of pe time for he exam CHOH CH.OH CHOH HA Provide a step-wise mechanism for the following equation, show intermediates and arrows for exchange of electrons.
- Tautomerization is a process in which an enol yields a ketone Give one examplefor a keto to enol tautomerization. Which form is more stable. Also, which ismore stable the E isomer or the Z isomer of 2-Chloro, 2-Butene22:43 10. Provide the following: the resonance structure of the intermediate that can resonate into the other intermediate that is given the product that results from the given resonance structure Specify which product is the kinetic product and which is the thermodynamic product . OH 50% H₂SO4 H~Which of the following will readily undergo decarboxylation upon heating?