Basically what
@bubba21 said, although I'd emphasis:
1.a. Learn the beginning chapters (resonance, chirality, R/S, E/Z, trans/cis, etc.) so well you could do them in your sleep. This will help tremendously later.
1.b. The same goes for SN1, SN2, E1, and E2. Etch the chart (primary, secondary, strong base/nucleophile, etc.) into your brain permanently.
2. As
@bubba21 said, don't fall behind. Be ahead if possible. The lecture should be review and not the first time you've seen the material.
3. Make GOOD flashcards for reactions. Use words instead of pictures. This forces you to both describe what is happening and to visualize it when you review the flashcards. If you can't visualize it, make a second set of flashcards specifically for that - "Nitrile - picture, Carboxyl group - picture, etc."
4. Mechanisms look complicated but they're really just applied knowledge. If you're studying hard, you should see patterns pretty early that repeat through Orgo 1 and 2. Mechanisms should be the easiest "gimme" as they're just memorization and you can pretty much just figure them out "on the go" if you have to.
Finally, don't underestimate Orgo. It's likely to be the toughest course you've taken so far by a good margin. Having said that, it's not uncrackable, just don't treat it like the other classes you've had so far.
I found Organic as a Second Language kind of useless if you're already using the main Klein book. Also: Do all the problems throughout the chapter - especially synthesis problems.