00:03
Suppose we want to predict the products of various different carboxylacic acid derivatives.
00:09
Well, in the first case, we have an alconol halide, and we're adding a thial to it.
00:16
And the key thing to note is thyls are very similar, very similar to alcohols in the way they function.
00:30
So, in fact, this will make something called a thioester, because it is that it is a very similar.
00:36
It's not exactly an ester because it isn't an alcohol being reacted.
00:43
Instead, it would be a sulfur atom instead of the alcohol.
00:48
But nonetheless, there is an ester bond, which is called a thioester bond.
00:55
But this functional group is a thioester.
00:59
And that will be our product.
01:02
What about in the next question? what about an alconol halide with excess ammonium or ammonia or an amine? rather excess amines.
01:15
Well, this will make an amide, this amide, plus we will have an ammonium salt, and that will be a side product, but it is still an organic product.
01:44
What about this example? we have an inhydride and an alcohol.
01:55
Well, it seems like it will be making an ester, which would be a correct assumption with a with a carboxylic acid group.
02:07
And i have drawn this poorly.
02:12
Let's try that again...