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- Provide reagents and reaction conditions for each stepDraw mechanism using pyradine as a base in the intial step Draw the mechanism using pydradine as a general base Draw the mechanism using pyradine as a nucleophilic catalyst Draw the mechanism using nucleophilic catalysis and using acetate as a general base H3C ROH ་ ་ CH3 N H3C -RNonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.
- Provide reagents and conditions to produce the products indicated. EN OH H3C CH3 HO HODraw a stepwise mechanism for the attached reaction that illustrateshow two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reactionconditions, even though it is a 1 ° alkyl halide.Pleas explain how this process occurs. Identify SN1, SN2, E2, E1, nucleophiles and electrophiles.