1) 2) Please give a detailed stepwise mechanism for the following reactions. All arrows, charges, and intermediates must be shown. NaOH, H₂O, heat я H₂O*, Bг₂ Br .. + HBr

Please help me with both of these problems, they are  the same question its just a two-part, I really want to study so please help

Show how you would carry out each of the following transformations.

Please give a detailed stepwise mechanism for the following reactions. All arrows, charges, and intermediates must be shown. 1) CN H*, H₂O, heat Яон OH

Bhu Please don't provide handwritten solution Write the mechanism of the reaction show with proper arrow formations. Do not combine in one step

Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.

Provide the mechanism for the following reaction (1) PhMgBr (2 equiv) (2) H3O+ workup OH

6-40 Give the substitution products expected from solvolysis of each compound by heating in ethanol. (a) (b) (c) Br (d) Br CI CH3 Br

Q2) a) Write a mechanism for the following reaction. 1.NH₂OH CI N N +ZnCl₂ 2. CINCI MeCN, Reflux 2 hr NH

Provide the products, intermediates, and/or reagents for the following reactions: