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- Select the reagents that will allow the following transformation(s) to occur. -H ? 1) NaOH 2) propyl bromide 1) Na2HSO4 2) propylanol 1) NaOH 2) propyl bromide 1) NaNH₂ 2) propyl bromideProvide reaction mechanisms for the following transformations1. Provide stepwise synthesis including reagents and intermediates for the following syntheses. OH COOH
- i) ii) 1. Propose a mechanism for the following reactions. H (CH3)2NH H* NaOH EtOH4) Provide a synthesis of the following compounds using the given starting material and any other reagents. starting material final product CI starting material final product OH OH OH starting material final product 5) Provide an arrow-pushing mechanism for the following reaction to get to the product shown. HON OH H₂O*, H₂O НО ملهProvide reagents needed to carry out the multi step synthesis
- Acetic acid has been mixed with isoamyl alcohol to produce isoamyl acetate giving off a banana smell. Propose a reaction mechanism for this reaction.Predict the product or provide reagents needed to complete each transformation.Predict the structure of compounds A and B and provide a mechanism for the reaction. OH CI HOO A H3O*
- Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. 1) CH3CH2M9B CH3OH H+ (ехcess) но 2) H30*, H2O B A OCH3Ethylene oxide is the starting material for the synthesis of 1,4-dioxane. Propose a mechanism for each step in this synthesis.Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.