00:01
So in this podcast, we're looking to predict the reaction products.
00:07
So first off, we start with our cyclopentan carbaldihyde.
00:10
This reacts with our methyl amine to form n cyclopentilometyline methamene.
00:19
So that looks as following.
00:25
Recyclic ring double bond to our nitrogen with a methyl.
00:37
Next, we have our cyclohexylene, which is a ketone.
00:43
React with pyrolydeen in the presence of an acid to form an anamine.
00:49
That looks as following.
00:50
So we have a heteratum in a cyclohexane ring.
00:56
Then we have another cyclohexene ring here though.
01:00
So that's a double bond.
01:01
So we have one cyclohex 1 -en, 1 -isle -ilidine.
01:13
Following this, we have an intramolecular reaction where the ketone and our primary amine when they are treated in the presence of an acid will lose a molecule of water and then we form a cyclical structure.
01:28
That looks as follows.
01:46
Next we have a cyclohexanone that reacts with a phosphorus yield to form an alkene derivative...