00:01
Hello, in here in cyclo.
00:05
In cyclohexene, in cyclohexen, there are two types of h present here.
00:22
Two types of h present.
00:23
One is axial, one is axial and another is equator.
00:32
If any bulky group present in an axial position, so there will be more repulsion.
01:04
And that is that confirms that confirmation would have would have higher energy so here compound structure is and compound structure is this one here so here is h and here is h here is h here is h here is h here is h here is h here is h here is h here is h here is h here is also h and here is h here.
02:03
So rotation this carbon here structure will be like this one here.
02:17
So rotation of carbon in this form here.
02:20
This one rotate here.
02:22
So here cyclohexing can be formed as like in this form here.
02:28
So this one is here and this one is here.
02:35
Right.
02:36
So here both.
02:37
Here is h here is h and in both case here is h here is h and here both h and here is h and here is h and here is also compound here so this one is a structure here and similarly for this one here another structure is this one here with h and h and here is with h and here is with h and here is o h and here is here is here already and here is h and h this one is b here so cyclohexene here is cyclohexene b has in this structure b so we can write b has more energy b has more b has more energy energy than a because oh because of oh contains, oh contain lawn pair, lawn, pair of e minus and will be, will cover more side, will cover more side.
04:10
So there will be, so there will be, so there will be more repulsion, more repulsion, hence it has, hence, it has higher, energy then a and for the compound b here similarly for option b here this one is trans three methyl three methyl cyclo hexinal so the product will be here here is h and here is ch3 similarly here is o h and here is h here is h here so the compound will be in here is h and here is ch3 here is h here is h here is h and here is oh and h here and h here is h here.
05:25
So this one is transposition and this position is cis here.
05:30
So in the transposition here so this transposition is unstable and will have high energy will have high energy will have high energy because of repulsion because of repulsion repulsion both bulky groups bulky groups and in the cis position here is stable this one is stable will have less energy less energy co2 of less interaction of loan pair and methyl group and methyl group here and for the last one option here for the third part see here here cis one metal our product is here cis one metal three one methanol cyclohexane cyclohexane here so here here product will be in this format here.
07:14
Here is in this form here...