Draw the major organic product of each reaction. Indicate the stereochemistry at the stereogenic center. Omit byproducts such as salts. If applicable, expand octets to minimize formal charges. SOCI₂ CH₂S- OH Pyridine Hill.... D product 1 Draw product 1. If the C-O bond breaks, assume inversion of configuration. product 2 Draw product 2. Select Draw Rings More Erase
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.
Draw the major organic product of each reaction. Indicate the stereochemistry
a.
![Draw the major organic product of each reaction. Indicate the stereochemistry at the stereogenic center. Omit byproducts such as
salts. If applicable, expand octets to minimize formal charges.
SOCI₂
CH₂S
OH Pyridine
Hll.
D
product 1
Draw product 1. If the C-O bond breaks, assume
inversion of configuration.
Select Draw Rings More
G
product 2
Erase
с H O D S cl
Q2Q
Draw product 2.
Select Draw Rings More
15
с
H O
Erase
D S cl
2 Q](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F8a98c306-c589-4f52-9305-c3af127d02d9%2F2667e120-d018-42af-bcec-ec1d11400adf%2Fshlznvi_processed.png&w=3840&q=75)
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