GRE Subject Test: Chemistry : Carbocations
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Example Questions
Example Question #1 : Carbocations
What intermediate is involved in the conversion of compound B to compound C?
Tertiary carbocation
Tertiary carbanion
Secondary radical
Secondary carbocation
Tertiary radical
Tertiary carbocation
The strong sulfuric acid protonates the hydroxyl group of compound B, resulting in the loss of water as a leaving group and the generation of a carbocation intermediate. Since this carbocation carbon is attached to three other carbons, this is a tertiary carbocation. It is bound to the phenyl substituent, a methyl group, and the branched carbon chain.
Example Question #241 : Organic Chemistry
Which of the following carbocation intermediates requires the least activation energy?
Cannot be determined
The more stable the carbocation, the lower the activation energy for reaching that intermediate will be. The more substituted a carbocation is, the more stable it is. The carbocation bonded to three alkanes (tertiary carbocation) is the most stable, and thus the correct answer.
Secondary carbocations will require more energy than tertiary, and primary carbocations will require the most energy.
Example Question #42 : Organic Chemistry
Carbon 1:
Carbon 2:
Let's say we react the given compound with 
Carbon 2 because the bromine will first attack the double bond from the least sterically hindered side
Carbon 1 because the bromine anion is large and requires space to react
Carbon 2 because the intermediate will be a secondary carbocation
Carbon 1 because the intermediate will then be a secondary carbocation
Carbon 1 because the intermediate will be a primary carbocation
Carbon 1 because the intermediate will then be a secondary carbocation
The correct answer is: carbon 1 because the intermediate will then be a secondary carbocation.
This is a case of 
If the hydrogen attached the carbon 2 then we would have a positive charge on carbon 1 and vice versa. A positive charge on carbon 1 is known as a primary carbocation (a carbon attached to 1 other carbon or function group), which is rarely if ever seen due to its overwhelming instability. A positive charge on carbon 2 is known as a secondary carbocation (a carbon attached to 2 other carbons or functional groups) and is much more stable than a primary carbocation.
We would want the more thermodynamically stable intermediate for our reaction to proceed, so we would want the positive charge on carbon 2 and the hydrogen attached to carbon 1.
Example Question #1 : Carbocations
If the carbon being pointed to was deprotonated (resulting in a positive charge on it). Would the resonance form (the positive charge being redistributed to the carbon with a bromine) be more stable than a secondary carbocation? Why?
Yes because bromine donates some electrons
Yes because bromine is an electrophile
No because bromine is an electrophile
No because secondary carbocations are unstable
No because bromine's bulky electron cloud will interfere
No because bromine is an electrophile
The resonance form of this compound would put the positive charge on the carbon attached to the bromine. Unfortunately this carbon is already slightly positive due to the electron withdrawing effects of bromine due to its high electrophilicity. So this resonance form would be more unstable than a secondary carbocation due to the increased concentration of positive charge from bromine's electron withdrawal.
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