Which of the following carbocations is the most stable?
- A$CH_3CH_2^+$
- B$CH_3^+$
- C$C_6H_5CH_2^+$
- D$CH_3CH_2CH_2^+$
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Similar Questions
What is the decreasing order of stability (most stable $\to$ least stable) of the following carbocations?
Medium
View SolutionWhich free radical is most stable among the following?
Which of the following is more stable than the remaining three?
Medium
View SolutionMatch the List-$I$ with List-$II$:
$A$. Carbocation $I$. Species that can supply a pair of electrons. $B$. Carbon free radical $II$. Species that can receive a pair of electrons. $C$. Nucleophile $III$. $sp^2$ hybridized carbon with empty $p$-orbital. $D$. Electrophile $IV$. $sp^2/sp^3$ hybridized carbon with one unpaired electron.
Choose the correct answer from the options given below:
| $A$. Carbocation | $I$. Species that can supply a pair of electrons. |
| $B$. Carbon free radical | $II$. Species that can receive a pair of electrons. |
| $C$. Nucleophile | $III$. $sp^2$ hybridized carbon with empty $p$-orbital. |
| $D$. Electrophile | $IV$. $sp^2/sp^3$ hybridized carbon with one unpaired electron. |
Choose the correct answer from the options given below:
Which of the following is the most stable carbanion?
Easy
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