00:05
And this question, we're drawing condensed structures for each of these compounds.
00:10
So a is two hexine.
00:12
So we'll have carbon one, two has the alkyne on it, three, four, five, six carbons.
00:21
There is two hexine.
00:23
Part b is five ethyl, three octane.
00:26
So that's eight carbons long.
00:29
So carbon one, oops, two, and then three has our alkyne on it for three octine.
00:35
Carbon four, five has an ethyl group on it.
00:41
And then six, seven, eight carbons.
00:47
C is methyl acetylene.
00:50
So acetylene looks, um, oops, looks like this.
00:56
It's just two carbons with a triple bond between them.
01:00
And to make it methyl acetylene, we'll replace one of those hs with a methyl group.
01:05
D is vinyl acetylene.
01:07
So again, we'll start with that two carbons with a triple bond.
01:10
And then we'll add a vinyl group on.
01:12
So that means a double bond.
01:14
So that would look like that.
01:17
This is our vinyl group.
01:20
E is methoxy ethine.
01:22
So ethine is the i -u -pac name for acetylene.
01:25
It's just those two carbons with the triple bond.
01:29
And then methoxy is an o -c -h -3 group.
01:31
It's an ether.
01:34
F is secbuttalene.
01:36
So again, we'll start with those triple bonds.
01:39
And then we have on one side, we have sec -beutal -a -turt -sadelene.
01:42
Butel...