00:01
Another podcast where we're just taking a look at reactions synthesis, retro -synthetic analysis, radical reactions.
00:06
We're really encompassing all of the topics that we've looked at so far, but in this summary podcast, we'll just look at the overall scheme, which will be just our starting material, our reagents, and our product.
00:26
So here we have our starting material.
00:29
Then we have quite a substantial amount of steps to access our product where our product is as follows still have that benzene ring and now we have two we have one ketone at the top and then at the bottom we have a chlorine group and then we have one more reaction to look at in part b where again i will just concern this podcast with the overall mechanism just to save time so in this first step, we have n -a -n -h -2.
01:34
Add e -t -i.
01:36
Second step, we have lind -lars -catalyst, which is h -2.
01:43
In our third step, we have n -b -s, which is our bromine source...