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

Suggest a reasonable mechanism for the reaction shown Br here. HO CH;CH,OH

i) ii) 1. Propose a mechanism for the following reactions. H (CH3)2NH H* NaOH EtOH

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

Please show a drawn mechanism, including intermediates where necessary for the reaction shown below. A drawn mechanism showing arrows and the movement of charges/electrons aids in understanding more than just walls of text.

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

The following reaction can be carried out in two steps. Choose the correct reagents i) and ii) to perform the following reaction. CN i) 11) or Oi) CN; ii) heat Oi) CN ; ii) H₂O, acid catalyst O i) Br₂; ii) CN- O i) H₂O, acid catalyst; ii) CN O i) HBr; ii) CN

Can you answer the question and explain it? With the mechanism  I ONLY CARE ABOUT THE ELIMINATION

Please explain how to solve

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