My Problems

Because the chlorine is more electronegative than iodine, the iodine will have a partial positive charge and will be attacked by the alkene. It forms the more stable carbocation as normal (as in problem 335). The nucleophile (HSCH₂CH₃) will eventually attack the carbocation, but the iodine does something special first- it forms a cyclic intermediate.

The formation of the cyclic halonium ion is probably the most important concept you will learn in first semester organic chemistry. With iodine, it's called an iodonium ion. (with chlorine or bromine, it's called a chloronium or bromonium ion). 

The HSCH₂CH₃ will attack the carbon that was the carbocation, but it's forced to attack from the side opposite to that of the iodine. So the product will always have anti stereochemistry (you get the trans product).

The first step in this reaciton, like many reactions, is an acid-base reaction- when you see an H⁺ (acid), the first step is usually something getting protonated. This starting material is a thiol (sulfur), but the same thing would happen with an alcohol or ether (oxygen).

When you have a protonated thiol (or alcohol, ether, etc.), you know the reaction isn't finished yet- products are rarely charged. There are two legal moves to get that positive charge off of the protonated thiol. Either the thiol deprotonates, or it takes off as a neutral leaving group. It can't deprontate because that would be going backwards, so your only "legal move" is for the HSCH₂CH₃ to act as a leaving group (See problem 518).

But then you're left with a carbocation, which is definitely not the final product. How can we get rid of it? (See problem 335 for general ways carbocations react). If the HSCH₂CH₃ attacked in an S_N1 type reaction that would be OK, but it would be going backwards! So the only way to get rid of the carbocation is to do a beta-elminiation (E1).

This is a acid-catalyzed hydration of an alkene, which is a Markovnikov addition. The product is an alcohol.

This is a hydroboration reaction (also called hydroboration-oxidation in some textbooks). The product is an alcohol.

Boron bonds to the less substituted carbon, and is replaced with an oxygen after the borane intermediate is treated with peroxide, resulting in an anti-Markovnikov addition. 

Note that one equivalent of BH₃ reacts with three equivalents of alkene; the borane intermediate is not BH₂(alkyl) but rather B(alkyl)₃.

This is a free radical halogenation. The hint is that you see light (hν) in the reaction arrow, indicating radicals are involved.

The more substituted the carbon atom, the more stable the corresponding radical, so the major product of this reaction is the 3º alkyl halide.

This is a substitution reaction. Because the reaction takes place in acid and the leaving group is on a 2º carbon, it will probably form a carbocation (S_N1 mechanism).

^-OH is a poor leaving group so the alcohol will protonate first, so it can leave as H₂O, which is neutral.

For a), the product is neutral and so you are done after the nucleophile (Cl-) attacks the carbocation.

For b), the the intermediate is a protonated alcohol, and so you must do a proton exchange step (also called a hydrogen exchange or deprotonation) to get the final alcohol product, which is neutral.

For c), there are two different types of beta hydrogens, and so two different alkenes are possible.

The more stable alkene is the one that will form, and this will always be the most highly substituted alkene. This is Zaitsev's rule. The rationale for this is hyperconjugation: neighboring carbon atoms stabilize an alkene.