Rank the following carbocations in order of increasing stability. H. A B O A B, D O D,A, B O B, A D O A D, B Which of the following reactions would result in a 50/50 mixture of stereoisomeric products? HBr ? ...... REACTION A HBr REACTION B O Both reaction A and B O Neither reaction A nor B O Reaction B O Reaction A Ozonolysis of molecule A would result in the formation of what two functional groups? A O Two Aldehydes O An Aldehyde and a Carboxylic Acid O A Ketone and an Aldehyde O Two Ketones
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.
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+)
H.
A
B
D
O A, B, D
O D, A, B
O B, A D
O A, D, B
Which of the following reactions would result in a 50/50 mixture of stereoisomeric products?
HBr
REACTION A
HBr
?
REACTION B
O Both reaction A and B
O Neither reaction A nor B
O Reaction B
O ReactionA
Ozonolysis of molecule A would result in the formation of what two functional groups?
A
O Two Aldehydes
O An Aldehyde and a Carboxylic Acid
O A Ketone and an Aldehyde
O Two Ketones"

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