но OCH2CF3 -CH=C -CH=C + CF;CH,OH -CH=C Н,о N=C CH3 H' ČH3 ČH3

H3C H3C H3C OH Amides can be hydrolyzed to yield carboxylic acids. The conditions are much more severe than those for other carboxylic acid derivatives. Acidic hydrolysis occurs by addition of water to the protonated carbonyl, followed by proton transfer to make the nitrogen a better leaving group. The reactions are reversible, and the reaction is driven to completion by protonation of NH3 at the end. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions NOC XT .H + NH3 NH₂ -OH H3O+ H₂O: NH3 H3C :0: OH NH3 H3O+

None

Perform the following synthesis. The number of steps in my path is provided. 5 steps OH SH

Label the reactants with either electrophile, nucleophile, base or acid.

Draw the mechanism for the reactions between the given carboxylic acid and -OH in H2O

Draw the entire extended reaction mechanism (curly arrows) for this reaction но- OH HO HO OMe H OMe OMe HO HO OMe

Please provide only typed answer solution no handwritten solution needed allowed