Answer:
Honestly makes no sense sorry :(
Explanation:
I can try though.. There are three types of selectivity possible for any synthesis: (i) Chemoselectivity is deciding which group reacts. (ii) Regioselectivity is where the reaction takes place in that group. (iii) Stereoselectivity is how the group reacts with respect to the stereochemistry of the product.
A stereospecific mechanism specifies the stereochemical outcome of a given reactant, whereas a stereoselective reaction selects products from those made available by the same, non-specific mechanism acting on a given reactant. Of stereoisomeric reactants, each behaves in its own specific way.
I tried to explain it the best I could.
Hopefully this helps you :)
Feel free to correct me If it was wrong
8
It’s 8 bc I said it was 8 ;)
Answer:
here is ur ans Lilly
Explanation:
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hope it's helpful for you mark brainlest where you from , age
To name this Alkyne, simply count from the direction that will give the lowest starting number to appear at the beginning of the carbon triple bond.
If you were to count from the top of the chain, the position of the carbon next to the triple bond would be 4. Yet if you count from the bottom chain going left to right and above the chain, the position of the carbon next to the triple bond would be 3.
Then identify the groups that are connected off the parent chain, here we have a methyl group on carbon 2.
Thus the name would be 2 - methyl - 3 - heptyne. I believe.
