Show how to carry out the transformation in the highest yield possible. Select the appropriate reagents and draw the correct organic product at each step. 1. CH3COCI 2. base reagent 1 reagent 2 product 1 product 2 + product 3 reagent 4 reagent 5 H2N- product 4 Identify reagent 1. Draw product 1. Select Draw Rings More Erase H N
Reactive Intermediates
In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.
Hydride Shift
A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.
Vinylic Carbocation
A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.
Cycloheptatrienyl Cation
It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.
Stability of Vinyl Carbocation
Carbocations are positively charged carbon atoms. It is also known as a carbonium ion.
 alt="Show how to carry out the transformation in the highest yield possible. Select the appropriate reagents and draw the
correct organic product at each step.
1. CH3COCI
2. base
reagent 1
reagent 2
product 1
product 2
+ product 3
reagent 4
reagent 5
H2N-
product 4
Identify reagent 1.
Draw product 1.
Select
Draw
Rings
More
Erase
H
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 alt="entify reagent 2.
Draw product 2.
Select Draw
Rings
More
Erase
| 7 | |
H
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