This might take a while, I'll probably have to come back to it later.
1. I would say how they do it (ie join nucleotides etc.)
2. RNA not DNA and they don't bind promoter sequences, they're synthesized
3. Okazaki are just fragments of ssDNA that form on the lagging strand as it is unwound by helicase, you don't really need more than that. The lagging strand is the one being synthesized in the 3' direction. I seriously doubt you'll be asked for definitions though.
3a. SCNT just gets the same genetic starter kit, there are plenty of other things that affect the genome (intra uterine environment, random mutation, etc.)
4. Trisomy 21 = 3 copies of 21 NOT the whole genome
5. Not at all times, but generally yes.
6. They replicate independently and are very easy to transfer between organisms, so they can confer new traits with relative ease. Worth pointing out that they're not produced by the bacteria, they're just parasites that hitch a ride.
7. You don't need to know the details
8. Produces only 2, genetically identical cells (clones). Can't remember the subtle other differences
9. Yes, just add the antibiotic to the dish you're plating on. Why would they already be antibiotic resistant, it's not like every bacterium is resistant to every antibiotic. Anyway, when you're working with bacteria and inserting a resistance plasmid to select certain ones, you will be using bacteria that specifically aren't resistant prior to plasmid transfection.