Chapter 8 Page 7 1) Conditions that have catalytic acid in excess weakly nuceophilic solvent 2) Most stable cation intermediate forms, which dictates where the incoming nucleophile ends up. 3)

Is a cation rearrangement via 1,2 hydride or methyl shift possible leading to a more stable cation? If so the hydride/methyl shift takes place before nucelophile addition. 4) When chirality centers are produced, both enatiomers are produced. Draw the arrows/ intermediates/products for the acid catalysed hydration reactions: Draw the arrows/ intermediates/products for the acid catalysed hydration reactions: Draw the arrows/ intermediates/products for the acid catalysed hydration reactions: + what other compound?